Company

Clinical ProfessionalsSee more

addressAddressHatfield, South Yorkshire
salary SalaryFull-time
CategoryConstruction & Property

Job description

Reference Number: JO-2306-518646
Qualified Person
Rate: Negotiable
Job Type: Permanent
Location: Hatfield

Almost 100% virtual role, only expected in Hatfield approx. 1 per quarter.

Must be UK qualified QP.

Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.

The Role & What You Will Be Doing

  • To carry out the duties and responsibilities of a Qualified Person as detailed in EU Directive 2001/83/EC and 2003/94/EC.
  • To ensure the principles and responsibilities of GMP and GDP, as stated in MHRA’s Rules and Guidance for Pharmaceutical Manufacturers and Distributors are interpreted and implemented correctly.
  • Participate in and manage the following quality systems.
  • Batch documentation review and subsequent batch disposition, including certification for release.
  • Sampling, inspection, batch processing and approval of bought-in products.
  • Liaison with contract laboratories and review of data generated following analysis.
  • Investigations into customer complaints.
  • Management of recalls of pharmaceutical products for the market.
  • Internal and external inspection programmes and to represent the department during regulatory inspections.
  • Review and processing of expired inventory, returns and rejects.
  • Maintain communication with third party warehouse, suppliers and line management.
  • To advise on activities relating to product quality ensuring compliance with registered particulars, GMP/GDP, and ensure supply issues are resolved in a timely manner and maintain stock levels.
  • Represent the department in new product introduction and product transfer processes and to provide comment on associated validation work.
  • Maintain communication with line management.
  • Aid in the training and mentoring colleagues in all aspects of GMP and other areas, as appropriate.
  • Business travel as required for technical meetings and project initiatives.
  • Meet annual objectives as agreed and carry out any other duties as directed by the Quality Vertical and UK Affiliate.

About Your Skills & Experience

For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:

  • BSc and or MSc in relevant scientific field
  • Eligible to act as a Qualified Person for the certification of marketed products in accordance with UK legislation
  • Excellent verbal and written communication skills with the ability to work independently and within dynamic / collaborative cross-functional team environments
  • Experience with communicating with the MHRA
  • Experience with various IT systems such as SAP, Documentum, Trackwise
  • Knowledge of manufacturing and packaging documentation, change control, qualification and validation process
  • Good decision-making skills, flexible to current and new situations

Refer code: 2594154. Clinical Professionals - The previous day - 2024-01-23 15:17

Clinical Professionals

Hatfield, South Yorkshire
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