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Stability Co-ordinator

A global leader in the manufacture of generic pharmaceuticals is looking to recruit a Stability Programme Co-ordinator for the North West Manufacturing site.


The main purpose of this position is to be responsible for managing the QC Chemistry stability programme, to supply quality stability data to support commercial manufacture of existing products on time, in full to the expected standard, to comply with global regulatory requirements and to review and approve analytical documents.


Key Results Area:

Compliance: to provide specialist knowledge to support the generation of quality stability data in compliance with cGLP, cGMP, Health & safety, SOPs and environmental and regulatory requirements.

Customer service: To deliver customer service by testing stability samples in an efficient and timely manner. To test components/raw materials/bulk, and finished product as required through flexible working.

Documentation: To complete all QC batch documentation, right first time, i.e. correct and in full, in order to achieve customer service and GMP

Provide training and guidance to other members of the department.

Lead laboratory investigations in accordance with company procedure.

Interpretation and implementation of technical protocols to facilitate method transfer activities

Qualifications/Experience:

Pharmaceutical experience with relevant science qualification, minimum HND.

Knowledge of pharmaceutical stability programme management

cGMP/ cGLP

Regulatory bodies/ customer requirements

Laboratory Analytical Techniques


The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. Carlisle Staffing plc, trading as SRG is an Employment Business/Agency.

SRG winners of the 2008 Recruiter Awards for Excellence: Best Candidate Care and Best Health Care/Medical Recruitment Firm.