Description
Job title: Business Analysis Coordination
Work location : Val de Reuil, France
Contract Dates: to
Salary: 70k€
Description:
Johnson & Johnson Consumer Products, a member of Johnson & Johnson's Family of Consumer Companies, is looking for an Analytical contractor to be located in Val-de-Reuil, France.
This contractor will work within the Life Cycle Management 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 compliance gap assessments but also for analytical test 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:
• Perform analytical compliance gap assessment versus current guidelines
• Manage multiple CROs and other external partners simultaneously
• Support analytical test method transfers
• Support analytical test method trouble shooting
• Support or initiate analytical test method improvement and validation
• Manage change control deliverables and CAPA activities relating to analytical remediation
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