Almac Sciences is seeking a dedicated and experienced Quality Manager to join our team at Edinburgh, Technopole. The team at Technopole manufacture peptides at small scale in accordance with cGMP, for clinical trial supply. The successful candidate will provide leadership, management and support to our Quality Assurance, Quality Control and Quality Validation teams, ensuring the implementation and maintenance of GMP compliant operations, supporting small scale Peptide Manufacturing operations for Clinical Trials. They are responsible for ensuring that cGMP compliance is maintained in accordance with regulatory and client expectations for Clinical Supply, whilst delivering to a varied operational portfolio and associated challenging timelines.
* Degree (or equivalent) in relevant Life Sciences or Analytical discipline.
* Significant experience in a Quality Management Role with responsibilities for Quality Assurance, Control & Validation within the Pharmaceutical Industry.
* Strong understanding of cGMP principles and regulatory requirements and significant, proven experience in a cGMP environment.
* Excellent communication, management and leadership skills of the wider Quality Team, Cross-Functional Stakeholders and Clients.
* Ability to manage multiple tasks and projects effectively, whilst facilitating the identification and deployment of creative solutions, as necessary.
For the successful candidate, we offer an attractive benefits package which will include a competitive salary, annual bonus, employer pension contributions, 34 days paid annual leave, healthcare benefits and much more. Please see further details on the Benefits Tab.
RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CVs received or submitted directly to Hiring Managers will be considered unsolicited, and no fee will be payable. Thank you for your cooperation.