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An established industry player is seeking a Quality Manager to oversee compliance in a GxP-licensed operation. This role offers the chance to lead quality initiatives, manage audits, and foster a culture of excellence. The successful candidate will be responsible for maintaining regulatory standards and will play a key role in the company's strategic growth. With a focus on continuous improvement and team leadership, this position is ideal for a driven professional looking to make a significant impact in the pharmaceutical sector.
Job Description
Blackfield Associates is currently partnered with a major pharmaceutical wholesale in the search for a Quality Manager – RP based in the midlands.
This position offers a unique opportunity to take ownership of a GxP-licensed operation, ensuring ongoing compliance with MHRA regulations across both wholesale and PI manufacturing arms of the business. As the named Responsible Person on the company’s WDA, you will carry personal accountability for maintaining the integrity and compliance of licensed activities, while also contributing strategically to the organisation’s growth and development.
Key Responsibilities:
The successful candidate will be Gold Standard RP certified and meet MHRA criteria to act as an RP, ideally with additional eligibility for RPi. You’ll bring a minimum of two years' experience in a GxP-regulated quality role, ideally within a wholesale or PI environment. A background in leading teams, managing audits, and driving continuous improvement is essential, as is familiarity with electronic QMS tools such as Q-Pulse, SAP, or Trackwise. While not a GMP expert, a solid working knowledge will be advantageous in this hybrid environment.
To apply, please send your most recent CV to Oliver@BlackfieldAssociates.com or contact Oliver on 02392 314 792.