Mantell Associates is partnered with a rapidly growing Pharmaceutical Manufacturing organisation who are seeking a Quality Manager to join their talented team to focus on QMS Management, Commercial Quality and RP responsibilities.

The successful candidate will be based in the Netherlands and can be onsite 2 days per week. This is a great opportunity for someone looking for the next step in the career and will give them a platform to obtain internal and external auditing experience and become a QP.

Quality Manager - Responsibilities:

• Oversee the New Product Introduction (NPI) process responsible for onboarding new customers and products to ensure successful clinical and commercial drug product manufacturing

• Lead the Product Quality Team responsible for disposition of batches, tracking batch release, and partnering with other departments to close out all required deliverables to support product disposition

• Develop and oversee the Quality on the Floor Program responsible for visual inspection and packaging operations

• Provide strategic guidance to resolve complex investigations and product quality issues

• Reviews and approves Commissioning and Validation protocols and final reports

• Reviews and approves QC stability study summaries, protocols, and final reports

Quality Manager - Requirements:

• Scientific degree and strong experience in Quality Assurance leadership in a GMP & GDP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility

• Proven experience managing a QMS

• GMP/GDP compliance knowledge

• Able to efficiently priorities workload across the team

• Team player with exceptional communication skills, a concern for excellence, ability to develop and mentor a team, and a high ability to collaborate with various levels of the organisation

Mantell Associates is a specialist Pharmaceutical and Life Sciences headhunting firm. For more information on this role, please contact us at +44 (0)20 3854 7700.