Lediga jobb Mcneil AB i Helsingborg

Kenvue is currently recruiting for a:
Planning Manager
What we do
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.
Who We Are
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.
Role reports to:
Senior Regional Supply Chain Manager
Location:
Europe/Middle East/Africa, Sweden, Skane, HelsingborgWork Location:
Fully Onsite
What you will do
The Production planning manager for Smoking Cessation is responsible for managing the planning and preparation of production schedules for manufacturing, implementing production planning policies, and analyzing production specifications to meet business goals:
**Key Responsibilities**
Team Leadership
Lead and mentor a team of planners and customer service, fostering a culture of efficiency, innovation, and continuous improvement.
Strategic Planning & Execution
Develop and implement production planning strategies tailored to the unique requirements of Smoking Cessation products. Lead the development of production schedules that align with customer demand, sales forecasts, and manufacturing capabilities.
Cross-Functional Collaboration
Collaborate with demand planning, quality, logistics and manufacturing teams to ensure seamless execution of production plans.
Operational Excellence
Monitor and maintain planning systems with up-to-date lead times, capacity data, and production specifications. Identify and resolve capacity constraints and operational bottlenecks to ensure on-time delivery. Improve the supply chain from production planning to market supply by optimizing service while balancing inventory and cost.
Data Analysis & Reporting
Utilize analytical tools to assess supply performance and identify areas for improvement. Prepare and present comprehensive production planning reports to senior management with actionable insights. Analyse shifting requirements from customers and markets and supporting the team with analysis and scenario planning.
Compliance & Governance
Ensure adherence to safety regulations, quality standards, and company policies in all planning activities. Manage the operational budget effectively and address backorder issues promptly.
Customer Focus
Establish strong communication channels with customers and production teams. Resolve complex production issues and customer complaints with a focus on satisfaction and service excellence.
What we are looking for
**Required Qualifications**
Strong Leadership and people management skills
Bachelor's Degree or Equivalent in a relevant field such as Supply Chain Management or Operations
8-10 years of experience in production planning within the healthcare or pharmaceutical industry
Demonstrated 8-10 years of experience in sales, operations, trade, and category management roles
Proven track record of successfully managing production planning processes for complex products
Proven track record of strong analytical skills and ability to interpret complex business data
Strong analytical skills and ability to interpret data to drive decision-making
Ability to prioritize and manage multiple projects/initiatives effectively
Experience working in a matrix environment and collaborating with cross-functional teams



**Desired Qualifications**
Strong negotiation skills and conflict resolution abilities
Excellent communication and leadership skills to effectively collaborate with cross-functional teams
Proficiency in syndicated data analysis and communication of insights
Exceptional interpersonal skills and relationship-building capabilities
Advanced computer skills, including MS Office Suite applications and sales database management
Ability to adapt to changing business requirements and drive results in a dynamic manufacturing environment



If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation. Visa mindre

Job Description
SCOPE OF THE POSITION:


The Site Finance Manager will provide direct financial leadership to the Helsingborg Site within the EMEA network, reporting to the Cluster Financial Controller. This role will partner with the Site Director, Site Leadership Team members, his/her direct reports and the Regional and Global Consumer SC organizations to achieve short/long term financial performance commitments and assess opportunities across sites that are in scope.


The Site Finance Manager will be responsible for Site business planning as well as the monitoring of actual results. He/she will partner with the Profitability Management & Reporting team to deliver insights into budget vs actual drivers, operational metrics, and frame results. Together with the Regional Finance Lead, this individual will propose/evaluate business cases (Capital, Investments, Site Master Plan, New Products) and support decision making with a focus on driving value. He/she will lead total cost per unit and GP impact analyses for the Site and provide guidance to the Site Leadership team on operational initiatives that are focused on optimizing costs and improving competitiveness for the Site.


This position will collaborate with Global Services, Centers of Excellence, and other centralized organizations on the financial review cycles to ensure the reliability of the financial information. He/she will provide insightful commentary on the financial drivers and communicate potential risks and opportunities. Together with the Site Leadership team this individual will be responsible for risk management and driving a compliance culture across the Site.


This role will identify and implement opportunities to enhance financial analytics and will also support process improvement and standardization initiatives led by Global Services and Centers of Excellence.


He/she will also take ownership for the performance and development of his/her direct reports.
MAIN ACCOUNTABILITIES:
· Business Partnering and Decision Support:
o Establish a collaborative relationship with the Site Director and well as the Site Leadership Team.
o Provide in-depth financial analysis and generate valuable insights to support business cases for investment decisions and cost savings opportunities.
o Actively contribute to the Site’s strategy and master plan.


· Performance Analytics and Reporting:
o Review and communicate performance on key financial drivers and metrics.
o Discuss variances between plan and actual results, share insights and recommend gap closure plans to the Leadership team.
o Identify potential risks and opportunities and lead discussions on associated action plans.


· Planning and Forecasting:
o Work with business partners to challenge assumptions, build models, review financial outputs and influence decision making.
o Present/Share the Site financial targets and budget to the Leadership team and Board to ensure strategic alignment.


· Product cost (standard costing) and pricing structure definition/review and maintenance.


· Risk Management and Compliance:
o Member of the Statutory Board with an oversight of internal controls for both US/SOX and local statutory requirements.
o Support internal/external audits, present audit outcomes to the board.
o Drive a culture of compliance across the Site.


· Support continuous improvements and best practices for financial processes/analytics and other ad hoc analyses/projects.




QUALIFICATIONS, EXPERIENCE AND SKILLS:


Education:
· Bachelor's degree in Accounting/Finance as well as a professional accounting qualification (Masters in Accounting/CA/CPA/CIMA)
· Fluency in Swedish, English, any other European Language would be a plus




Required competencies and experience:


· 6+ years of progressive finance experience, preferably Supply Chain Finance experience.
· Strong leadership skills to develop and implement a vision
· High conceptual and analytical competence
· Ability to zoom in and out – ability to focus on process-oriented tactical plans as well as big picture strategic thinking to challenge status quo
· Collaboration and Business Partnering
· Well-developed storytelling and communication skills
· Results and performance driven
· Excellent problem-solving skills
· Autonomous working attitude with high motivation
· Developing and motivating people
· Ability to work under pressure whilst paying attention to detail


Systems:
· SAP ERP and advance skills in MS Office. Knowledge of Business Intelligence systems would be an advantage.


Preferred:


· Consumer Goods Industry Experience


Location:


· Helsingborg, Sweden Visa mindre

Kenvue is currently recruiting for a:


Planning managerWhat we do
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.
Who We Are
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.
Role reports to:
Regional Planning Senior ManagerLocation:
Europe/Middle East/Africa, Sweden, Skane, HelsingborgWork Location:
Fully OnsiteWhat you will do
The Production planning manager for Smoking Cessation is responsible for managing the planning and preparation of production schedules for manufacturing, implementing production planning policies, and analyzing production specifications to meet business goals:


**Key Responsibilities**
Team Leadership
Lead and mentor a team of planners and customer service, fostering a culture of efficiency, innovation, and continuous improvement.
Strategic Planning & Execution
Develop and implement production planning strategies tailored to the unique requirements of Smoking Cessation products. Lead the development of production schedules that align with customer demand, sales forecasts, and manufacturing capabilities.
Cross-Functional Collaboration
Collaborate with demand planning, quality, logistics and manufacturing teams to ensure seamless execution of production plans.
Operational Excellence
Monitor and maintain planning systems with up-to-date lead times, capacity data, and production specifications. Identify and resolve capacity constraints and operational bottlenecks to ensure on-time delivery. Improve the supply chain from production planning to market supply by optimizing service while balancing inventory and cost.
Data Analysis & Reporting
Utilize analytical tools to assess supply performance and identify areas for improvement. Prepare and present comprehensive production planning reports to senior management with actionable insights. Analyse shifting requirements from customers and markets and supporting the team with analysis and scenario planning.
Compliance & Governance
Ensure adherence to safety regulations, quality standards, and company policies in all planning activities. Manage the operational budget effectively and address backorder issues promptly.
Customer Focus
Establish strong communication channels with customers and production teams. Resolve complex production issues and customer complaints with a focus on satisfaction and service excellence.
What we are looking for


**Required Qualifications**
- Strong Leadership and people management skills
• Bachelor's Degree or Equivalent in a relevant field such as Supply Chain Management or Operations
• 8-10 years of experience in production planning within the healthcare or pharmaceutical industry
• Demonstrated 8-10 years of experience in sales, operations, trade, and category management roles
• Proven track record of successfully managing production planning processes for complex products
• Proven track record of strong analytical skills and ability to interpret complex business data
• Strong analytical skills and ability to interpret data to drive decision-making
• Ability to prioritize and manage multiple projects/initiatives effectively
• Experience working in a matrix environment and collaborating with cross-functional teams
**Desired Qualifications**


• Strong negotiation skills and conflict resolution abilities
• Excellent communication and leadership skills to effectively collaborate with cross-functional teams
• Proficiency in syndicated data analysis and communication of insights
• Exceptional interpersonal skills and relationship-building capabilities
• Advanced computer skills, including MS Office Suite applications and sales database management
• Ability to adapt to changing business requirements and drive results in a dynamic manufacturing environment
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation. Visa mindre

Kenvue is currently recruiting for:
Automation Engineer
This position is based at site Helsingborg, Sweden.
Who we are
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands — including OTC brands such as NICORETTE®, IPREN®, LIVOSTIN®, IMODIUM®, PEPCID® and consumer health brands like NEUTROGENA®, LISTERINE®, NATUSAN®, PIZ BUIN® and o.b. ®. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes.
The Kenvue site in Helsingborg, Sweden is the home of the strong and growing brand NICORETTE®, a global market leader in smoking cessation. In 2021 our production facility was recognized as a Lighthouse by World Economic Forum, marking us as a beacon in The Fourth Industrial Revolution.
The Helsingborg site is one of the largest employers in the city of Helsingborg, and the business is divided in two separate departments: Operations, where we house our manufacturing activities and R & D, our global development center for excellence working in three therapeutic areas for selfcare treatments: Smoking Cessation, Digestive Health and Cough & Cold. For more information, click here
What you will do
The Automation Engineer is responsible for serving as a senior-level, independent contributor with expertise in automation area. You will independently solve problems and resolve issues within your area of expertise.
Key Responsibilities
Automation Support to production
System responsible for one or several automation systems. (Fulfillment of production needs and regulations requirements)
Provide technical guidance and support to technicians in the automation systems.
Collaborate and work on small to medium size technical/automation projects
Ensure compliance with relevant regulations and provide necessary documentation.

What we are looking for
Required Qualifications
Ca 10 years of experience in Automation engineering
Good Knowledge of Advance Automation systems and infrastructure, including hardware, software, and networking.
Experience of production support
Analytical and problem-solving skills
Prior knowledge in one or several of following automation concepts: DCS, PLC/SCADA, MES or Vision/Serialization systems.
Experience in OT Cyber Security.
Full proficiency in Swedish & English

Desired Qualifications
Knowledge in one or several of the following system Siemens PCS7/Batch, PROCOS DCS, AVEVA system platform
Knowledge in Antares Vision/serialization systems
Understanding of compliance landscape and regulatory environment.
Experience from Food/Pharma industries, or other FMCG.

What’s in it for you
Competitive Total Rewards Package
Paid Company Holidays, Paid Vacation, Volunteer Time & More!
Learning & Development Opportunities
Employee Resource Groups

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.
Background checks in the recruitment process
As a final candidate in our recruitment process, you may be subject to a background check. This process is important for us to ensure the quality of our recruitment process.
As part of this, it is important that we encourage you to make sure that the information in your CV is correct before submitting your application to us.
To carry out these background checks, we use a background check company. Different checks may be carried depending on the position that you are applying for. This could be, for example:
Reference checks
CV-validation
Financial checks
Litigation checks, including criminal cases

The background check company is an independent data controller for any personal data that they will process during the check, and if you have any questions about the processing, you may turn to the background check company.
Due to our business activities and daily operations, we may also carry out drug tests as part of our recruitment process. Visa mindre

Kenvue is currently recruiting for:
Lab Systems Automation Lead
This position reports to the Senior Manager - QA Systems & Applications and is based at Helsingborg, Sweden.


Who we are
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands — including OTC brands such as NICORETTE®, IPREN®, LIVOSTIN®, IMODIUM®, PEPCID® and consumer health brands like NEUTROGENA®, LISTERINE®, NATUSAN®, PIZ BUIN® and o.b. ®. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes.
The Kenvue site in Helsingborg, Sweden is the home of the strong and growing brand NICORETTE®, a global market leader in smoking cessation. In 2021 our production facility was recognized as a Lighthouse by World Economic Forum, marking us as a beacon in The Fourth Industrial Revolution.


What you will do
The Lab Systems Automation Lead is responsible for providing site level support for the Kenvue laboratory systems (LIMS, Empower, SDMS, ComplianceBuilder). Primary responsibilities include implementation of solutions in the Kenvue laboratories to automate processes related to instrument data transfer and driving laboratories towards a paperless laboratory environment through electronic lab notebooks and test method execution.
Additionally this role will identify improvement areas, and recommend process changes to correct issues improve lab processes. This role will also support the resolution of system related issues and fixes, master data setup, and automation of lab processes via LIMS system connections and test scripts.


Key Responsibilities
Integration Execution and Support
Design and implement automation solutions for Kenvue lab systems to ensure seamless integration of laboratory data from standalone instruments.
Develop and standardize the maintenance of scripts and standard protocols for instrument integration
Design, implement, and maintain integrations between laboratory instruments and information management systems (LIMS). Ensure that laboratory systems are interconnected to facilitate efficient data flow.
Lead integration projects from concept through to implementation, ensuring all milestones and deadlines are met.
Coordinate with IT, laboratory staff, and external vendors to execute integration projects. Provide technical support and troubleshooting for laboratory systems and integration issues.
Provide support for projects to build electronic lab notebook templates in conjunction with IT
Ensure all integrations comply with industry standards and local regulatory requirements. Implement security protocols to protect sensitive laboratory data.
Develop and maintain documentation related to integration SOPs, User Guides, protocols, etc. Ensure the accuracy and integrity of data transferred between systems. Work with data management teams to enhance data quality and reporting capabilities.
Conduct training sessions for laboratory staff on new systems and integration processes. Keep up-to-date with the latest technologies and best practices in laboratory integration.

LIMS Project and Platform support
Provide support and troubleshooting for Kenvue LIMS system in conjunction with the global business and IT teams
Support alignment of site/regional requirements for new LIMS system implementations and enhancements that align with Global solution and design.
Support Global Master data community of practices so that master data requirements are adopted consistently across internal manufacturing sites. Where applicable support updates and implementation of master data objects relevant to the business requirements and processes.
Recommend changes to methods and procedures to address improvement areas
Write, review and modify standard test/operational procedures
Lead and participate on process improvement teams



Qualifications
What we are looking for
Required Qualifications
Bachelor's degree in Computer Science or related field
6-8 years of experience in automation engineering or LIMS/laboratory management systems (including Labware pharma template experience), or any combination thereof
Experience in Software Development Lifecycle (SDLC) methodologies and computer system validation required
Programming acumen for LIMS file based integration
Excellent problem-solving and analytical skills
6-8 years related experience in quality control process analysis
Experience in process improvement methodologies
Professional fluency in Swedish & English

Desired Qualifications
Experience with automation tools such as Selenium, Jenkins, and Robot Framework
Excellent communication and interpersonal skills
Proficiency in data analysis tools and techniques

What’s in it for you
Competitive Total Rewards Package
Paid Company Holidays, Paid Vacation, Volunteer Time & More!
Learning & Development Opportunities
Employee Resource Groups



Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.
Background checks in the recruitment process
As a final candidate in our recruitment process, you may be subject to a background check. This process is important for us to ensure the quality of our recruitment process.
As part of this, it is important that we encourage you to make sure that the information in your CV is correct before submitting your application to us.
To carry out these background checks, we use a background check company. Different checks may be carried depending on the position that you are applying for. This could be, for example:
Reference checks
CV-validation
Financial checks
Litigation checks, including criminal cases

The background check company is an independent data controller for any personal data that they will process during the check, and if you have any questions about the processing, you may turn to the background check company.
Due to our business activities and daily operations, we may also carry out drug tests as part of our recruitment process. Visa mindre

Kenvue is currently recruiting for:
Process Improvement Engineer
This position reports to Packaging Business Unit and is based at our Stattena site in Helsingborg, Sweden.
Who we are
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands — including OTC brands such as NICORETTE®, IPREN®, LIVOSTIN®, IMODIUM®, PEPCID® and consumer health brands like NEUTROGENA®, LISTERINE®, NATUSAN®, PIZ BUIN® and o.b. ®. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes.
The Kenvue site in Helsingborg, Sweden is the home of the strong and growing brand NICORETTE®, a global market leader in smoking cessation. In 2021 our production facility was recognized as a Lighthouse by World Economic Forum, marking us as a beacon in The Fourth Industrial Revolution.
The Helsingborg site is one of the largest employers in the city of Helsingborg, and the business is divided in two separate departments: Operations, where we house our manufacturing activities and R & D, our global development center for excellence working in three therapeutic areas for selfcare treatments: Smoking Cessation, Digestive Health and Cough & Cold. For more information, click here.


What you will do
As our Process Improvement Engineer, you will be at the forefront of our continuous improvement journey, driving world-class manufacturing operations that meet customer expectations in terms of safety, quality, reliability, and cost targets. Your expertise in process analysis and improvement methodologies will be crucial to our ongoing success.


Key Responsibilities
Lead Continuous Improvement initiatives: Coordinate and implement activities to maximize productivity, efficiency, and optimize costs while reducing waste and process variability. You'll analyze existing production processes to identify inefficiencies, bottlenecks, and areas for improvement.
Support site OKRs: Drive process improvements using established methodologies and benchmark best practices of Kenvue Operating Excellence (KOE), Quality, and Safety.
Support product/project pipeline: Contribute expertise to new product introductions and changes to existing products
Serve as Process SME: Manage User Requirement Specifications (URS) and process-related documents after approval
Material testing - Perform and document testing of new/updated materials.

Qualifications
What we are looking for
Required Qualifications
Further education in relevant field
Proven experience in process improvement within the Manufacturing industry.
Strong analytical skills with proficiency in data analysis tools.Project management and communication skills.
Outstanding ‘lean attitude’ and willingness/ability to learn fast
Complete professional proficiency in both Swedish & English
Good knowledge of MS Office

Desired Qualifications
Lean / Six Sigma / Green Belt certification would be a plus

What’s in it for you
Competitive Total Rewards Package
Paid Company Holidays, Paid Vacation, Volunteer Time & More!
Learning & Development Opportunities
Employee Resource Groups



Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.
Background checks in the recruitment process
As a final candidate in our recruitment process, you may be subject to a background check. This process is important for us to ensure the quality of our recruitment process.
As part of this, it is important that we encourage you to make sure that the information in your CV is correct before submitting your application to us.
To carry out these background checks, we use a background check company. Different checks may be carried depending on the position that you are applying for. This could be, for example:
Reference checks
CV-validation
Financial checks
Litigation checks, including criminal cases

The background check company is an independent data controller for any personal data that they will process during the check, and if you have any questions about the processing, you may turn to the background check company.
Due to our business activities and daily operations, we may also carry out drug tests as part of our recruitment process. Visa mindre

Team Lead - Produktion
Den här befattningen lyder under Business Unit Manager och är baserad i Helsingborg.


Vilka vi är
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re
the house of iconic brands — including OTC brands such as NICORETTE®, IPREN®, LIVOSTIN®, IMODIUM®, PEPCID® and consumer health brands like NEUTROGENA®, LISTERINE®, NATUSAN®, PIZ BUIN® and o.b. ®. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes.

The Kenvue site in Helsingborg, Sweden is the home of the strong and growing brand NICORETTE®, a global market leader in smoking cessation. In 2021 our production facility was recognized as a Lighthouse by World Economic Forum, marking us as a beacon in The Fourth Industrial Revolution.

The Helsingborg site is one of the largest employers in the city of Helsingborg, and the business is divided in two separate departments: Operations, where we house our manufacturing activities and R & D, our global development center for excellence working in three therapeutic areas for selfcare treatments: Smoking Cessation, Digestive Health and Cough & Cold.

Vad du kommer att göra
Team Lead är ansvarig för att arbeta aktivt med sitt team av operatörer och tekniker för att uppnå definierade avdelningsmål
och nyckeltal, som en del av företagets mål (Business Plan). Agera som en förebild och ambassadör för Kenvue Way och driva
arbete som ökar medarbetares välbefinnande och engagemang.


Key Responsibilities
• Skapa en Compliance kultur och efterleva de standarder som gäller för Compliance när det gäller EHS och kvalitet samt säkerställ att behov av utbildning uppfylls
• Leverans av resultat enligt uppsatta KPIer, såsom t ex OEE, SA, kostnader och inför åtgärder vid behov
• Planera, leda och genomföra arbete med ständiga förbättringar (Continous Improvement) med hjälp av de verktyg
som finns i KOE (Kenvue Operating Excellence) såsom t ex problemlösning och grundorsaksanalys tillsammans med
operatörer/tekniker med även korsfunktionellt.
• Utvärdera och planera förbättringsaktiviteter framåt inom verksamheten och avrapportera status till sponsor/stakeholder.
• Leda och arbeta med NC/CAPA samt i projekt som berör avdelningen
• Dokumentera, utföra och avrapportera uppföljningar/sammanställningar samt skapa/uppdatera dokumentation
såsom t ex SOP/JobAids som berör avdelningen
• Utveckla och coacha teamet av medarbetare att uppfylla deras mål och utvecklingsmål genom att regelbundet utföra samtal och ge feedback samt aktivt arbeta med Shopfloor program och 5S-program
• Planera resurser/arbete på ett optimalt sätt för operatörer och tekniker och arbeta aktivt med att utöka flexibilitet mellan och inom avdelningar. Vara kontaktperson vid behov av flexibel arbetsstyrka/konsulter och följa upp certifieringsplaner tillsammans med certifierare och initiera behov av ny certifiering.
• Följ eskaleringsmodellen och agera kontaktperson vid behov av eskalering eller som mottagare vid samarbeten utanför avdelning (kontaktperson mot supportfunktioner, chefer, beredskap, mm).
• Arbeta aktivt tillsammans med övriga TL för att utbyta information, planera samt benchmarka andra avdelningar/grupper

Vad vi söker
Kvalifikationer som krävs
• Minst 3 års erfarenhet inom en ledande befattning inom produktion.
• Full förståelse för tekniska termer och förmåga att effektivt förmedla information till supportfunktioner och
intressenter/stakeholders.
• Stark problemlösningsförmåga och beslutsfattande kompetens.
• Komplett färdighet i kommunikation på svenska och engelska (både tal och skrift).
• Yrkeskunskaper i Microsoft Office-applikationer inklusive Word, Excel, PowerPoint och Sharepoint.

Önskade kvalifikationer
• Tidigare erfarenhet av sex sigma-/processutmärkelseverktyg
• Erfarenhet av arbete inom en reglerad produktionsmiljö
Vad du får ut av det
• Konkurrenskraftigt förmånspaket
• Betalda företagsresor, betald semester, flextid, och mer!
• Möjligheter till lärande och utveckling
• Resursgrupper för medarbetare

Kenvue är stolta över att vara en arbetsgivare som erbjuder lika möjligheter för alla. Samtliga kvalificerade kandidater kommer att övervägas för anställning utan hänsyn till ras, hudfärg, religion, kön, sexuell läggning, könsidentitet, ålder, ursprung, eller skyddad veteranstatus och kommer inte att diskrimineras på grund av funktionsnedsättning.


Background checks in the recruitment process
As a final candidate in our recruitment process, you may be subject to a background check. This process is important for us to ensure the quality of our recruitment process.
As part of this, it is important that we encourage you to make sure that the information in your CV is correct before submitting your application to us.
To carry out these background checks, we use a background check company. Different checks may be carried depending on the position that you are applying for. This could be, for example:
Reference checks
CV-validation
Financial checks
Litigation checks, including criminal cases

The background check company is an independent data controller for any personal data that they will process during the check, and if you have any questions about the processing, you may turn to the background check company.
Due to our business activities and daily operations, we may also carry out drug tests as part of our recruitment process. Visa mindre

Kenvue is currently recruiting for:
Automations Elektriker
Den här befattningen lyder under Maintenance Supervisor och är baserad i Stattena, Helsingborg.
Vilka vi är
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands — including OTC brands such as NICORETTE®, IPREN®, LIVOSTIN®, IMODIUM®, PEPCID® and consumer health brands like NEUTROGENA®, LISTERINE®, NATUSAN®, PIZ BUIN® and o.b. ®. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes.
The Kenvue site in Helsingborg, Sweden is the home of the strong and growing brand NICORETTE®, a global market leader in smoking cessation. In 2021 our production facility was recognized as a Lighthouse by World Economic Forum, marking us as a beacon in The Fourth Industrial Revolution.
The Helsingborg site is one of the largest employers in the city of Helsingborg, and the business is divided in two separate departments: Operations, where we house our manufacturing activities and R & D, our global development center for excellence working in three therapeutic areas for selfcare treatments: Smoking Cessation, Digestive Health and Cough & Cold. For more information, click here
Vad du kommer att göra
MAM (Make asset management) söker nu en Automations Elektriker. Närmsta teamet består av 6 stycken medarbetare, som ingår i MAM organisationen med totalt ca. 40 medarbetare. Gott samarbete värdesätts högt internt i teamet såväl som externt med andra avdelningar och leverantörer. Glädje och humor värdesätts och gör arbetsdagen så mycket trevligare.
Arbetstiden är dagtid med beredskapstjänstgöring
Huvudsakliga ansvarsområden
Underhåll och service av vår automatiserade produktions miljö.
Felsökning i el- och styrsystem.
Deltagande i projekt och förbättringsarbete för att effektivisera vår maskinpark.
Läsa och hantera el-dokumentation.

Vad vi söker efter
Du bör vara drivande, innovativ och ha god samarbetsförmåga. Eftersom din roll syftar till att skapa tekniska förutsättningarna för att vi ska nå våra nyckeltal, är det viktigt att du är flexibel och serviceinriktad.
Kvalifikationer som krävs
Minst gymnasieutbildning inom el/automation eller motsvarande utbildning.
Goda kunskaper i både Svenska och Engelska, verbalt och skriftligt.
Grundläggande datorförståelse, t.ex Microsoft Office.
Grundläggande PLC programmering/felsökning.
B-körkort.

Önskade kvalifikationer
Programmering/felsökning i PacDrive 3 Automation.
Kunskaper inom ritningsarbete, utförs idag i Elprocad.

Vad du får ut av det
Konkurrenskraftigt förmånspaket
Betalda företagsresor, betald semester, flextid, och mer!
Möjligheter till lärande och utveckling
Resursgrupper för medarbetare

Kenvue är stolta över att vara en arbetsgivare som erbjuder lika möjligheter för alla. Samtliga kvalificerade kandidater kommer att övervägas för anställning utan hänsyn till ras, hudfärg, religion, kön, sexuell läggning, könsidentitet, ålder, ursprung, eller skyddad veteranstatus och kommer inte att diskrimineras på grund av funktionsnedsättning

Background checks in the recruitment process
As a final candidate in our recruitment process, you may be subject to a background check. This process is important for us to ensure the quality of our recruitment process.
As part of this, it is important that we encourage you to make sure that the information in your CV is correct before submitting your application to us.
To carry out these background checks, we use a background check company. Different checks may be carried depending on the position that you are applying for. This could be, for example:
Reference checks
CV-validation
Financial checks
Litigation checks, including criminal cases

The background check company is an independent data controller for any personal data that they will process during the check, and if you have any questions about the processing, you may turn to the background check company.
Due to our business activities and daily operations, we may also carry out drug tests as part of our recruitment process. Visa mindre

Kenvue is currently recruiting for:
Sr Scientist EMEA Translational Science R&D
This position reports to Director EMEA Translational Science R&D and is based in Helsingborg, Sweden.
Who we are
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands — including OTC brands such as NICORETTE®, IPREN®, LIVOSTIN®, IMODIUM®, PEPCID® and consumer health brands like NEUTROGENA®, LISTERINE®, NATUSAN®, PIZ BUIN® and o.b. ®. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes.
The Kenvue site in Helsingborg, Sweden is the home of the strong and growing brand NICORETTE®, a global market leader in smoking cessation. In 2021 our production facility was recognized as a Lighthouse by World Economic Forum, marking us as a beacon in The Fourth Industrial Revolution.
The Helsingborg site is one of the largest employers in the city of Helsingborg, and the business is divided in two separate departments: Operations, where we house our manufacturing activities and R & D, our global development center for excellence working in three therapeutic areas for selfcare treatments: Smoking Cessation, Digestive Health and Cough & Cold. For more information, click here


What you will do
The Sr Scientist, EMEA Translational Science R&D serves as a consumer and clinical strategy lead for innovation or renovation projects across all consumer health categories, with a primary focus on Cough and Cold. The role involves significant collaboration across many different functions within Kenvue. This position will, in close collaboration with cross functional partners, evaluate innovation opportunities, lead the creation of a fit for purpose end-to-end consumer learning plan and execute defined studies.
This position will specifically have responsibility in creating consumer research strategies, planning research, act as study manager and report the outcome of such studies to project teams, stake holders and management.
This role involves extensive cross-functional and global/cross-regional team matrix interactions
Key Responsibilities:
Responsible for designing consumer research studies in partnership with selected vendors and Kenvue cross functional teams
Act as study manager and lead cross functional teams to assure studies are executed as per plan and company procedures
Apply owners mindset by constantly looking for opportunities to strengthen and accelerate study methodology, protocol design and execution models
Represent Translational Science (across consumer and clinical research) in the cough and cold need state development team
Assure appropriate claims and consumer learning plans are developed for EMEA lead product innovation and major renovation projects
Partner closely with Consumer Business Intelligence, Product Design and Commercial teams to assure alignment of study objectives and plans
Partner with regulatory and medical affairs to assure plans meets regulatory and relevant industry association requirements
Engage with senior management, the wider translational science community and brand teams to share research outcomes
Maintain an outside-in perspective with required credible partnerships to assure that we continue to advance our capabilities with improved and new methodologies to help drive stronger claims, higher quality studies, as well as faster and more cost effective execution



What we are looking for
Required Qualifications
Bachelor's degree with at least 5+ years or Master’s degree with 3+ years of relevant work experience in consumer self-care (OTC, Medical devices and Food supplements) product development, design and consumer research
Proven experience of consumer research for the OTC medicine category
Experience of consumer research from other consumer health categories (e.g. cosmetics, hair care)
Experience from partnering and leading research with consumer research agencies
Experience in OTC medicine product development and analytical testing
Must have experience of leading project teams as well as strong skills in collaboration, communication, leadership and ability to effectively explain scientific concepts.
Candidates need to be proficient with Microsoft Office, Word, Excel, and PowerPoint and have strong oral and written communication skills in English.
R&D experience from the Cough and Cold OTC category
Experience from working with products in multiple regulatory classifications (food supplements, OTC medicines, cosmetics,…)
Have an understanding of consumer brand fundamentals


What’s in it for you
Competitive Total Rewards Package
Paid Company Holidays, Paid Vacation, Volunteer Time & More!
Learning & Development Opportunities
Employee Resource Groups


Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.
Background checks in the recruitment process
As a final candidate in our recruitment process, you may be subject to a background check. This process is important for us to ensure the quality of our recruitment process.
As part of this, it is important that we encourage you to make sure that the information in your CV is correct before submitting your application to us.
To carry out these background checks, we use a background check company. Different checks may be carried depending on the position that you are applying for. This could be, for example:
Reference checks
CV-validation
Financial checks
Litigation checks, including criminal cases



The background check company is an independent data controller for any personal data that they will process during the check, and if you have any questions about the processing, you may turn to the background check company.
Due to our business activities and daily operations, we may also carry out drug tests as part of our recruitment process. Visa mindre

Kenvue is currently recruiting for:
MAM Lead
Location: Helsingborg
Who we are:
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours.
The MAM Lead is responsible for providing engineering and Maintenance guidance and direction to the Helsingborg Site ensuring they are delivering “best-in-class” approaches with respect to all elements of engineering and reliability maintenance practices. This person will actively work by: Supporting strategic decisions related to Helsingborg Site, Providing Flawless Execution knowledge related to capital equipment & facility upgrades and Maintenance programs, Point of contact between the Site and the regional Technical Operation organization, and Supporting engineering related urgent issues during the execution or manufacturing phases.
Responsibilities:
Responsible for the Site Engineering and Reliability Maintenance through: People Development plan execution, Teaching and Coaching and Feedback/Evaluation
Responsible for Site Project portfolio consolidation through: Connection with Site Leadership
Direct, guide and provide oversight for the site CapEx portfolio including forecasting, prioritizing budgeting, controlling and reporting of the site capital plan, communicating status and health to site and network stakeholders.
Responsible for Site Project portfolio Execution through: Site team performance Management
Responsible for Innovation at site level through: Need identification through connection to Site Leadership, upper level management etc.
Responsible to develop Continuous improvement approach
Role modelling and Promoting Root Cause Problem Solving
Responsible for Standard deployment at Site level through: Responsible for Compliance (Quality & Safety, Environment, IH and sustainability) related activities\initiatives at Site level
Coordinate the development of the Technical Site Master Plan and manufacturing asset replacement strategy based on asset condition assessment, applying value analysis and incorporating results into the CapEx portfolio.
Coordinate asset Reliability and manage technical issues related to manufacturability
Owns Site Machine Safety
Support for developing department annual budgets, and monitoring/controlling budget performance. Ensures sound management of head count and expenses to meet approved spending plan and site functional targets
Accountable to deliver the Site Reliability & Maintenance KPI/targets to improve Site performances
Determine appropriate local allocation of staffing managing the process for utilization of contracted staff and services where appropriate. Ensure contracts and agreements are in place to provide an adequate labor pool, and works with vendor leadership to manage performance as needed
Assure local assets and operations are used and conducted in a safe manner and in full compliance with all EHS and regulatory agency requirements


Qualifications
A Bachelor’s Degree of Engineering (or University equivalent) and a minimum of 10 years of (functional and/or people) experience in an OTC/Pharma (manufacturing/technical) environment is required
Experience in People Management
Ability to drive engineering operational excellence across the organization with measurable, financial, quality and cycle time results is required
Experience in Engineering Project Management
Experience managing the site capital portfolio
Knowledge across Corrective, Planned and Reliability maintenance
Proven ability to work effectively and drive alignment in a matrix management environment through effective communication, collaboration and influence
Strong understanding of the Asset Management and NPI (new product introduction) processes.
Fluent in English language – writing, speaking and understanding


What’s in it for you:
Competitive Benefit Package
Paid Company Holidays, Paid Vacation, Volunteer Time & More!
Learning & Development Opportunities
Employee Resource Groups

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Background checks in the recruitment process
As a final candidate in our recruitment process, you may be subject to a background check. This process is important for us to ensure the quality of our recruitment process.
As part of this, it is important that we encourage you to make sure that the information in your CV is correct before submitting your application to us.
To carry out these background checks, we use a background check company. Different checks may be carried depending on the position that you are applying for. This could be, for example:
· Reference checks
· CV-validation
· Financial checks
· Litigation checks, including criminal cases
The background check company is an independent data controller for any personal data that they will process during the check, and if you have any questions about the processing, you may turn to the background check company.
Due to our business activities and daily operations, we may also carry out drug tests as part of our recruitment process. Visa mindre

Kenvue is currently recruiting for:
Senior Packaging Development Engineer
This position reports into the Associate Director Packaging and is based at Helsingborg, Sweden


Who We Are
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands — including OTC brands such as NICORETTE®, IPREN®, LIVOSTIN®, IMODIUM®, PEPCID® and consumer health brands like NEUTROGENA®, LISTERINE®, NATUSAN®, PIZ BUIN® and o.b. ®. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes.
The Kenvue site in Helsingborg, Sweden is the home of the strong and growing brand NICORETTE®, a global market leader in smoking cessation. In 2021 our production facility was recognized as a Lighthouse by World Economic Forum, marking us as a beacon in The Fourth Industrial Revolution.
The Helsingborg site is one of the largest employers in the city of Helsingborg, and the business is divided in two separate departments: Operations, where we house our manufacturing activities and R & D, our global development center for excellence working in three therapeutic areas for selfcare treatments: Smoking Cessation, Digestive Health and Cough & Cold.

What You Will Do
The Senior Engineer Global Packaging EMEA is responsible to lead and coordinate the development and qualification of primary, secondary and tertiary packaging in a variety of Self Care projects together with a wide range of internal and external partners and stakeholders. You will be the packaging technical expert in those multi type of projects. For example in new product development, reformulation, quality and compliance, improvement of existing packaging, qualification of equivalent packaging materials or additives, mold duplication, packaging cost improvement, plant support, improvement of products profitability.
You will join a stable, growing company in times that in many other industries are marked by instability. This is a challenging role, where you will get to develop and constantly learn. If you have aspirations on becoming a leader in the future, this role is the right stepping stone.
Key Responsibilities
Collaborate with cross functional partners in EMEA to define the packaging brief and regional needs
Coordinate the creation/modification/improvement of packaging in collaboration with global hubs and external partners, covering packaging development, qualification and implementation
Identify and evaluate technical solutions, including seeing to those materials are aligned with relevant regulation and guidelines
Define & execute the packaging development plan
Analyze and validate packaging technical drawing with the support of experienced packaging team members or manager
Contribute to innovation, develop consumer understanding and identify new ideas
Initiate and own critical documentation, to track and follow changes
Create Packaging component specifications, validate finished product specifications
Generate packaging documentation for product release



What We Are Looking For
Required Qualifications
A degree within a relevant area linked to package engineering, polymer or mechanics
At least 7 years working experience within packaging development
Good and versatile knowledge of packaging technologies – materials, molding processes, manufacturing
Familiarity with the process of developing drugs and/or medical devices
Strong packaging sensibility and interest in promoting the importance of packaging in the product experience
Proficient professional skills in English
Visa to work in the EU



Desired Qualifications
Experience in packaging development within the pharmaceutical and/or medical device industry.
Experienced working in complex FMCG project environment. Good communication, influencing and flexibility skills to manage ambiguity linked to high matrix environment and turn complex cases into synthetic recommendations.
Self-motivated and results-driven, able to easily connect with remote stakeholders or peers.
Curious, creative and the able to translate ideas into concepts and projects. Engaged and can challenge status-quo to drive globalization while managing regional constraints



What’s In It For You
Competitive Benefit Package
Learning & Development Opportunities
Paid Company Holidays, Paid Vacation & More!
Employee Resource Groups



Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Visa mindre

Kenvue is currently recruiting for:
Sr Scientist - EMEA Translational Science R&D
This position reports to Director EMEA Translational Science R&D and is based in Helsingborg, Sweden.
Who we are
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands — including OTC brands such as NICORETTE®, IPREN®, LIVOSTIN®, IMODIUM®, PEPCID® and consumer health brands like NEUTROGENA®, LISTERINE®, NATUSAN®, PIZ BUIN® and o.b. ®. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes.

The Kenvue site in Helsingborg, Sweden is the home of the strong and growing brand NICORETTE®, a global market leader in smoking cessation. In 2021 our production facility was recognized as a Lighthouse by World Economic Forum, marking us as a beacon in The Fourth Industrial Revolution.

The Helsingborg site is one of the largest employers in the city of Helsingborg, and the business is divided in two separate departments: Operations, where we house our manufacturing activities and R & D, our global development center for excellence working in three therapeutic areas for selfcare treatments: Smoking Cessation, Digestive Health and Cough & Cold. For more information, click here

What you will do
The Sr Scientist, EMEA Translational Science R&D serves as a consumer and clinical strategy lead for innovation across all consumer health categories, with a primary focus on Cough and Cold. This position works closely with cross-functional teams to evaluate innovation opportunities within their assigned segments, need states or brands and create a fit for purpose end-to-end consumer learning plan for the initiative.
This position will specifically have responsibility in creating consumer research strategies, planning research, act as study manager and report the outcome of such studies to stake holders and management.
This role involves extensive cross-functional and global/cross-regional team matrix interactions.


Key Responsibilities:
Responsible for designing consumer research studies in collaboration with selected vendors and Kenvue cross functional teams
Act as study manager and lead cross functional teams to assure studies are executed as per plan
Apply owner’s mindset by constantly looking for opportunities to strengthen study methodology, protocol design and execution models
Represent Translational Science (across consumer and clinical research) in selected brand development teams
Assure appropriate claims and consumer learning plans are developed for EMEA lead product innovation project
Partner closely with R&D, Consumer Business Intelligence and Commercial teams to assure alignment of study objectives and plans
Partner with regulatory and medical affairs to assure plans meets regulatory requirements
Engage with senior management and brand teams to share research outcomes
Maintain an outside-in perspective with required credible partnerships to assure that we continue to advance our capabilities with improved and new methodologies to help drive stronger claims, higher quality studies, as well as faster and more cost-effective execution

What we are looking for
Required Qualifications
Bachelor's degree with at least 5+ years or Master’s degree with 3+ years of relevant work experience in consumer self-care (OTC, Medical devices and Food supplements) product development, design and consumer research
Proven experience of consumer research for the OTC medicine category
Some level of experience of consumer research from other consumer health categories (e.g. cosmetics, hair care)
Experience from partnering with consumer research agencies
Experience in OTC medicine product development and testing
Must have experience of leading project teams as well as strong skills in collaboration, communication, leadership and ability to effectively explain scientific concepts.
Candidates need to be proficient with Microsoft Office, Word, Excel, and PowerPoint and have strong oral and written communication skills in English.
R&D experience from the Cough and Cold OTC category
Experience from working with products in multiple regulatory classifications (food supplements, OTC medicines, cosmetics,…)
Have an understanding of consumer brand fundamentals



What’s in it for you
Competitive Total Rewards Package
Paid Company Holidays, Paid Vacation, Volunteer Time & More!
Learning & Development Opportunities
Employee Resource Groups Visa mindre

Kenvue rekryterar för närvarande till:
Företagssköterska
Denna position rapporterar till EHS Site Lead och är baserad i Helsingborg (Sverige).

Vilka vi är
På Kenvue tror vi på den kraften i daglig omtanke och omvårdnad. Våra klassiska varumärken, som NEUTROGENA®, AVEENO®, LISTERINE®, JOHNSON'S® och BAND-AID®, används dagligen av miljoner människor världen över. Kenvues medarbetare omfamnar digitalisering och innovation som viktiga hörnstenar i företagets utveckling, där målet är att varje dag förtjäna en plats i konsumenternas hem och hjärtan.
Kenvue i Helsingborg tillverkar det starka och växande varumärket NICORETTE®, en världsledande produkt inom rökavvänjning. År 2021 utsågs vi till ett Lighthouse av World Economic Forum, vilket innebär att vi är en ledstjärna i den fjärde industriella revolutionen. Hållbarhet är en del av vårt DNA och sedan 2020 är vår produktion certifierad som koldioxidneutral över alla energikällor.
Anläggningen i Helsingborg är en av de största arbetsgivarna i Helsingborgs stad, med totalt cirka 680 anställda - 590 inom Operations och 90 inom R & D. Vår R & D-avdelning är ett globalt center för forskning och utveckling inom tre områden: Rökavvänjning, maghälsa samt hosta och förkylning.

Vad ska du göra
Huvudsakliga ansvarsområden:
Kartlägga hälsostatus, identifiera risker, analysera resultat och föreslå lösningar och förbättringsåtgärder inom ansvarsområdet.
Arbeta med en helhetssyn på hälsa och livssituation för både individen och gruppen.
Uppföljning av lagstiftning och koncernkrav inom ansvarsområdet, samt uppföljning av efterlevnad av dessa inom Kenvue.
Samordna vaccinationer (årlig influensa)
Delta i projekt och miljögrupper.
Delta i utredningar av olycksfall, händelser och risker i arbetet.
Planera och genomföra utbildning och information inom ansvarsområdet.
Ansvarig för medicinsk verksamhet med bedömning, rådgivning, behandling och uppföljning av patienter.
Aktivt bidra till att skapa en ökad säkerhetskultur på Kenvue.
I samarbete med EHS deltar kollegor och chefer i att upprätta, implementera och upprätthålla en effektiv och snabb process för screening före placering och passformstestning, inklusive nödvändig uppföljning i enlighet med lokal lagstiftning.
Inkludera den anställde i relevanta program för medicinsk övervakning vid behov.
Om ett hälsoproblem har konstaterats vid screeningen före placeringen, delta i eller ge råd om hur riskbedömningar på arbetsplatsen ska göras och vidta rimliga anpassningsåtgärder för att minimera rollens inverkan på hälsotillståndet.
Samordna drogtestningen om det krävs i företagets policy och lokal lagstiftning.



Vad vi söker
Kvalifikationer
Sjuksköterskeexamen med svensk legitimation
Arbetslivserfarenhet inom arbetsmiljö
Utmärkt kommunikations- och organisationsförmåga
Utmärkt förmåga att kommunicera på svenska och engelska, både muntligt och skriftligt
Helhetssyn och social kompetens
Har ett hälsofrämjande synsätt och ett genuint intresse för människor.


Meriterande
Arbetslivserfarenhet inom företagshälsovård eller liknande, där arbetsuppgifterna innehållit koppling till arbetsmiljö och stressrelaterade problematik
Trygg i dig själv och självgående


Vi erbjuder
Vi är en företagshälsovård och en professionell oberoende resurs för företagets främjande, förebyggande, utvecklande och efterhjälpande arbete. Som företagshälsovård har vi en god kunskap om arbetsplatserna och har möjlighet att över tid följa människor och se dem växa, lyckas och utvecklas. Vårt uppdrag är att arbeta allt från förebyggande med arbetsmiljöfrågor på individ-, grupp- och organisatorisk nivå till behandling av arbetsrelaterad ohälsa. En mycket viktig del i vår verksamhet är att skapa och upperätthålla ett väl fungerande samarbete med alla avdelningar inom företaget.
Vi är ett team som består av företagsläkare, arbetsmiljöingenjörer, företagssköterska, medicinsk sekreterare och administratör.
Vi erbjuder ett arbete med omväxlande arbetsuppgifter hos ett passionerat företag intresserad av sina medarbetare. Visa mindre

What We Are Looking For
As a person, you are positive, energetic and orderly, and in order to thrive in the role, it is important that you are service-oriented and enjoy variety in your work. You have a good ability to lead others and are a skilled communicator with the ability to adapt your communication to the recipient. You have a strong interest in sustainability and technical management. You are curious, development- and solution-oriented and value quality highly and are good at creating good relationships around you. We also see that you have good leadership skills and knowledge in control and regulations, project management, property management as well as good experience from energy optimization and authority requirements.
What You Will Do
The and directs facility and energy projects or studies including complete projects requiring advanced knowledge of a specialized field. Oversees projects, leads facility staff, and coordinates vendors and contractors. Applies complex and expert knowledge of engineering principles and practices within broad assignment areas. Acts as energy champion and work for continuous improvements in that area. Reports directly to SR Facility Manager and acts as representative in designated areas.
Key Responsibilities
Plans and directs facility and security projects or studies including complete projects requiring advanced knowledge of a specialized
Oversees projects, leads engineering staff, and coordinates vendors and
Applies complex and expert knowledge of engineering and facility principles and practices within broad assignment
Monitors safety and environmental operations to meet requirements for the site. Assists in the completion of safety and environmental action plan
Researches and monitors best practices and factors performance metrics and guides members of the facility organization in inventory and cost
Assist to ensure preventive maintenance of building utilities and machinery, manufacturing systems, mechanical and electromechanical equipment, and provides complex laboratory
Administers major facilities and security
Recommends estimates for base design costs including equipment, installation, labor, materials, preparation and other related
Oversees construction and installation and stays up-to-date on established codes, corporate requirements, specifications and
Guides and provides examples, based leadership to facility
Researches energy saving projects, determines payback periods, and manages energy projects to
Responsible for the high level day to day energy
Partner with EHS&S regarding project safety and contractor
Maintain Capital Delivery Process and facilitate its use and continual improvement and benchmarking including CIP
Actively manage, prioritize, and screen project portfolio to meet capital budgets and the needs of the
In co-operation with key figures within facility & security (Facility Manager, HVAC supervisor, Hard services engineer etc.) direct and lead resources in line with strategical
Acts as representative to Facility Manager in assigned projects and day to day tasks both within the facility organization and on site

Required Qualifications
Degree in civil, university engineering or
Several years of experience from the property industry and especially in a project management
Good knowledge of the Office package, software and other technical
Driver's
Speaks and understands both Swedish and English fluently,

What’s In It For You
Competitive Benefit
Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays &
Learning & Development
Employee Resource Groups

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Visa mindre

Laboratory Engineer
We are looking for driven laboratory engineer who wants to be a part of our team to support the core business with analyses and to work with improvements on daily basis.
Your main tasks will be quality control of finished product and the laboratory mainly uses chromatographic analysis techniques. The primary data is documented/managed electronically in Labware/ LIMS (Laboratory Information Management System).
The work is done in accordance with GMP.
Within QC Lab, we work flexibly between the groups and thus the tasks can include analysis of both raw material, packaging material, finished goods and microbial analyzes.
The position is fixed term during three years from October 2023, if possible. For right candidate there is also good opportunity to grow in the position.

Qualifications
degree in chemistry, micro or other relevant education (required)
demonstrate ability to work in a fast-paced diverse team environment and individuals while taking personal responsibility for decisions and driving results (required)
experience of chemical analyzes and knowledge of chromatographic techniques such as LC and GC (required)
experience of work in microbiological laboratory (merit)
demonstrate independent understanding and application of core GMP fundamentals, including but not limited to: Data Integrity (DI), Good Manufacturing Practices (GMPs), and Good Documentation Practices (GDPs).
good language skills in Swedish and English both written and spoken (required)
experience of working in lab is required, knowledge of LIMS and Empower a merit.
basic computer (Microsoft Office: Word, Excel)

What you need to succeed is
a team player
ability to collaborate flexible in an agile environment.
solution-oriented mindset
both technical and social competence skills.
ability to be pro-active and work independently as well as in team.
to be structured and communicate well is required.
the ability to continuously work with improvements in the daily work.

What’s In It For You
Competitive Benefit Package
Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!
Learning & Development Opportunities
Employee Resource Groups
This list could vary based on location/region

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Visa mindre

McNeil AB manufactures NICORETTE ® products for the global market. In addition to production, we also have a research and development department that works in three areas: Smoking Cessation, Digestive Health, and Cough & Cold. We are one of the Helsingborg region's largest workplaces and a number of different professional areas are represented here. Our goal is to be an inspiring workplace and by being part of Johnson & Johnson we can offer exciting challenges in an international environment.


We are proud that NICORETTE ® - the world's first product for smoking and tobacco use, was developed and developed by us in Helsingborg. The first idea was to alleviate the withdrawal of various occupational groups who could not smoke during working hours. The very first product became a nicotine gum that was launched in Switzerland in 1978. Today, NICORETTE ® is a world-leading product found in over 80 countries.


Focusing on the priorities from implementing the new Consumer Business model, we are now reorganizing the manufacturing group, recruiting for a Site Lead, Make Asset Management (MAM). MS&T is a center led MAKE Team consolidating capabilities from Global Technical Operations (GTO), Global Make Engineering (GME), Maintenance, and SMP manufacturing support activities into ONE organization at a cluster and regional level. MAKE Asset Management will be structured around 4 functions: Reactive Maintenance (line support), Preventive maintenance (planned), Pro-active maintenance (Reliability) and Design/ Project execution/ Commissioning & Qualification (Engineering)


Reporting directly to the Manufacturing, Sciences & Technology (MS&T) Cluster Leader for the region, the Site Lead, Manufacturing Asset Management (MAM), In partnership with the Site Leader and Site Leadership Team, is responsible for providing strategic and technical leadership and tactical direction to the diverse and highly skilled team of Engineers, Maintenance Leads, Maintenance Technicians and Capital Project Managers passionate about driving and delivering efficient cost, safety, quality and compliance for the Helsingborg site manufacturing assets.


Specifically, the Site Lead will:
Provides strategic direction and planning for the engineering and maintenance functions at the site, identifying and leading initiatives to drive execution excellence and timely realization of the site goals and objectives.
Directs, guides and provides guidance for the site CapEx portfolio.
Owns the development of the Site Master Plan and manufacturing asset replacement strategy based on asset condition assessment, applying value analysis and incorporating results into the CapEx portfolio.
Owns asset Reliability elements from asset creation (system), PM design, spares strategy, to technical issues related to manufacturability
Is responsible for developing department annual budgets, and monitoring/controlling budget performance. Ensures sound management of headcount and expenses to meet approved spending plan and site functional targets
Leads the local Maintenance Agenda and oversees adherence to best practices and processes as adopted across the Supply Chain (JJOS-Manage Site assets) and the Consumer Health Maintenance CoE.
Engages, inspires, coaches and develops peers and subordinates toward the objectives of enhanced job performance, technical knowledge, career satisfaction, and professional development and growth.
Is responsible for ensuring the ISA-95 level 1 and 2 systems and associated operation is compliant and fit for intended use in accordance with applicable standards and procedures throughout systems lifecycle
Partners with MS&T Technology Strategy & Innovation team, Cluster leads and Enterprise in the design and delivery of appropriate contracts and agreements for contracted services, provided an adequate labor pool for all needed services
Works in close collaboration with EFM (Facilities) in terms of resource leveraging (reliability, planning, scheduling, spare parts), Technology application (Schad, CbM, CMMS) and Work processes eg maintenance support model



Required Qualifications
Bachelor's Degree in Engineering, Science or related technical field mandatory.
Advanced Degree (Masters) in Engineering or MBA is helpful
Minimum twelve (12) years of meaningful business experience
Minimum of six (6) years of supervisory / people management experience with proven success in performance management and development
Experience in conceptual development, design and implementation, planning and scheduling and project management of capital projects ranging in value from 500K to 5 Mio USD.
Ability to work effectively and drive alignment in a matrix management environment through effective communication, teamwork, and influence
Engineering and / or Maintenance experience in an operational environment within FDA or other regulated industry
Proficient in English language – writing, speaking and understanding



We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Visa mindre