Pharmacy Manager - Medicines Evaluation Unit Ltd, IQVIA business
Listed on 2026-02-05
-
Healthcare
Pharmacy Technician -
Pharmaceutical
Pharmacy Technician
Location: Wythenshawe
Overview
Pharmacy Manager – GMP Pharmacy & Manufacturing. Full Time.
The Medicines Evaluation Unit, an IQVIA business, is one of the UK’s leading contract research organisations conducting clinical trials for the pharmaceutical industry. The organisation holds MHRA Phase I Accreditation, together with an MHRA Manufacturing Licence MIA (IMP). Our state-of-the-art facility operates under strict Good Manufacturing Practices (GMP).
RoleWe are seeking a detail-oriented, proactive Pharmacy Manager to join our production team. As a Pharmacy Manager, you will assist the Head of Pharmacy to support operational functions of the MEU pharmacy department and GMP manufacturing facility. You will play a key role in supporting the preparation, packaging, dispensing and quality control of pharmaceutical products. This management role combines accuracy with strict compliance to Good Manufacturing Practice (GMP) guidelines.
Responsibilities- Assist the Head of Pharmacy to support operational functions of the MEU pharmacy department and GMP manufacturing facility.
- Support preparation, packaging, dispensing and quality control of pharmaceutical products.
- Ensure compliance with GMP guidelines and regulatory requirements.
- Registered Pharmacist (GPhC) or equivalent relevant scientific qualification (e.g. Registered Pharmacy Technician).
- Significant experience in GMP sterile and non-sterile manufacturing, IMP handling, or clinical trial pharmacy operations.
- Strong working knowledge of EU GMP, GCP, UK Clinical Trials Regulations, and MHRA inspection requirements.
- Proven leadership and team management skills within a regulated environment.
- Excellent documentation, organisational, and communication skills.
- Demonstrated ability to manage workload and make decisions under inspection-ready conditions.
- Experience with in an MHRA Phase I unit, CRO, or early-phase manufacturing environment.
- Experience with aseptic or sterile manufacturing.
- Knowledge of QMS tools, CAPA management, and risk-based approaches.
- Experience supporting facility design, qualification, or expansion projects.
- Proactive, accountable, and quality-driven with strong attention to detail.
- Confident and calm under pressure with sound professional judgement.
- Collaborative and adaptable, capable of leading multidisciplinary teams.
- Committed to maintaining the highest standards of GMP and GCP compliance.
- Competitive Salary & Benefits Package
- A supportive, safety-focused working environment
- 29 days annual leave plus bank holidays
- Company pension scheme
- Discretionary bonus and healthcare plan after a qualifying period
- Free secure on-site parking
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