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Pharmacy Manager - Medicines Evaluation Unit Ltd, IQVIA business

Job in Wythenshawe, Manchester, Greater Manchester, M9, England, UK
Listing for: Jobster
Full Time position
Listed on 2026-02-05
Job specializations:
  • Healthcare
    Pharmacy Technician
  • Pharmaceutical
    Pharmacy Technician
Job Description & How to Apply Below
Position: Pharmacy Manager - Medicines Evaluation Unit Ltd, an IQVIA business
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).

Role

We 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.
Essential qualifications
  • 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.
Desirable qualifications
  • 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.
Personal attributes
  • 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.
MEU will offer you
  • 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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