Johnson & Johnson Consumer Products, a member of Johnson & Johnson's Family of Consumer Companies, is looking for an Analytical consultant to be located in Helsingborg, Sweden, Val-de-Reuil, France or Maidenhead, UK. This consultant will work within the Global Technical Operations (GTO) analytical section and support marketed OTC products primarily within the EMEA/APAC regions. A close collaboration with internal and external manufacturers, CROs, t... Visa mer
Johnson & Johnson Consumer Products, a member of Johnson & Johnson's Family of Consumer Companies, is looking for an Analytical consultant to be located in Helsingborg, Sweden, Val-de-Reuil, France or Maidenhead, UK. This consultant will work within the Global Technical Operations (GTO) analytical section and support marketed OTC products primarily within the EMEA/APAC regions. A close collaboration with internal and external manufacturers, CROs, the GTO formulation development and the GTO deployment organisation will be important.
General Job Scope
To provide desktop support mainly for analytical test method transfers but also for analytical method development, method validation and quality control activities for a series of product transfers.
Quality and Technical desktop support would include but not be limited to
• Manage multiple CROs and other external partners simultaneously
• Support analytical test method transfers
• Support product manufacturing transfer from analytical perspective
• Support analytical test method trouble shooting
• Support or initiate analytical test method improvement and validation
• Manage the testing requirements for product, raw material and packaging components to relevant GMP standards
• Manage change control deliverables and CAPA activities relating to analytical testing and transfers
Experience Required
Educational – Minimum of a Master’s degree with a major in chemistry or related sciences.
Work Experience and personal characteristics required
• A minimum of 5 years in an analytical laboratory role supporting pharmaceutical manufacturing, product development or quality assurance with a major emphasis on analytical method development, optimization, validation, verification, transfer and product testing. Experience with multi-ingredient liquid and solid-dose formulations essential
• Experience and deep knowledge with HPLC/UPLC, GC, dissolution and other major analytical techniques
• You need to be an innovative and a creative problem solver who can work independently, while managing multiple priorities successfully. The ability to influence others without direct line authority is highly preferred. You need to have both a team spirit and leadership skills. Strong written and oral communication skills are highly valued. Experience from working in a matrix organization is desirable.
• Comprehensive understanding of quality and regulatory compliance knowledge, pharmacopeia including USP, EP, ICH/WHO guidelines and good understanding of GxP systems
• Technical writing and documentation review abilities
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