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CMC Manager

Job in Portsmouth, Hampshire County, PO5, England, UK
Listing for: Alliance Medical
Full Time position
Listed on 2026-03-01
Job specializations:
  • Healthcare
    Healthcare Management
Salary/Wage Range or Industry Benchmark: 60000 - 80000 GBP Yearly GBP 60000.00 80000.00 YEAR
Job Description & How to Apply Below

We have a new opportunity for a Chemistry, Manufacturing, and Controls (CMC) Manager to join our Radiopharmacy team.

As CMC Manager the role holder will support current and new radiopharmaceutical development projects by planning and implementing local CMC activities with a close collaboration in cross‑functional teams, and work to develop and execute local CMC strategies aligned with business objectives and regulatory requirements from product development to the commercialisation phases.

The CMC Manager will assist in the implementation & maintenance of production processes and quality control testing, writing, and updating GMP documents and ensuring compliance with cGMP and assisting in document reviews and approvals by supporting the quality assurance workflow.

The CMC Manager will also hold responsibility for reporting the progress to update the contractors or performing on site visits as appropriate.

Our benefits include 5 weeks holiday, discounted private health insurance and a pension plan.

Alliance Medical operates a robust pre‑employment screening process for all roles which includes the following checks:
Identity, right to work in the UK, Professional registration and qualifications, Employment history and references (for the previous 5 years), Criminal record and bannings (Standard or Enhanced DBS check) and Occupational health assessments. All offers of employment are subject to satisfactory completion of these checks.

Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date.

To be successful in this role you should be able to demonstrate:

  • University degree in pharmaceutical sciences, chemistry or related scientific discipline.
  • Strong understanding of cGMP regulations and regulatory requirements for radiopharmaceuticals.
  • At least 2 years of radiopharmaceutical industry experience in production or quality control and quality assurance.
  • Experience in technology transfer projects.
  • Ability to identify and solve complex problems.
  • Ability to think out of the box and challenge current CMC development strategies.
  • Being a team player with good communication skills.
  • Willing to travel in Europe (max. 10%).
  • Willing to work in a remote team.
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