In brief
This Quality Assurance Manager role oversees site quality systems and leads a dedicated team within a pharmaceutical manufacturing environment. The work involves managing departmental performance, ensuring strict adherence to GMP standards, and coordinating complex quality investigations alongside internal and external audits.
Best for
Experienced pharmaceutical quality managers with an aseptic or sterile manufacturing background
Non-negotiable
4+ years of experience in Quality Assurance within a pharmaceutical setting
Worth knowing
This is a full-time, on-site role based in Reading, Monday to Friday.
What you need
Required
Quality Assurance
4+ years
People management
Clearly required in the listing
GMP knowledge
Clearly required in the listing
Aseptic manufacturing
Clearly required in the listing
Internal auditing
Clearly required in the listing
Regulatory compliance
Clearly required in the listing
Scientific degree
Clearly required in the listing
PrOFS
Clearly stated in the job description.
Preferred
EQMS
Clearly stated in the job description.
LIMS
Clearly stated in the job description.
Your day-to-day
Manage QA department personnel
Clearly stated in the job description.
Lead quality management meetings
Clearly stated in the job description.
Perform internal audits
Clearly stated in the job description.
Review quality documentation
Clearly stated in the job description.
Support regulatory inspections
Clearly stated in the job description.
Maintain quality documentation
Clearly stated in the job description.
Coordinate quality systems
Clearly stated in the job description.
Experience expected
Level
Senior level
Based on what the listing states
Years of experience
4+ years
of relevant experience stated for this role
Clearly stated in the listing
Evidence from the listing
Years required
“…vant scientific area or equivalent experience in a pharmaceutical setting A strong background in Quality Assurance (4 years+) Aseptic or Sterile manufacturing background Good regulatory knowledge (GMP…”
Experience level
“…partment and Site Management Team People management for the QA Department as required, including managing of workloads, setting objectives and performance development Operational oversight of Quality…”
Full job description (from employer)⌄
Looking for a QA role that challenges your thinking as much as it values your expertise? Join an award-winning global Pharmaceutical company dedicated to improving patient outcomes through quality excellence and state-of-the-art technology. We have an exciting opportunity for an experienced Quality Assurance Manager to join the established Quality team The Role: Full Time, Monday to Friday, On-site As a QA Manager, you will be an active member of the Quality Department and Site Management Team People management for the QA Department as required, including managing of workloads, setting objectives and performance development Operational oversight of Quality Assurance Officers, Document Controller, Admin and Quality Support Officer, including responsibility for absence, sickness, and overtime Coordinate with the Head of Quality, Lead QP, QPs, Senior QA Manager and other QA Managers in maintaining and improving the Global Quality system Lead Site Quality Management Meetings, document and track actions, and proactively drive the resolution of identified issues Perform and/or oversee internal audits in accordance with the internal audit schedule and ensure spot checks are being performed Participate in MHRA inspections and client audits as site host alongside the Head of Quality Support the introduction and development of an eQMS and/or LIMS system Serve as the Quality SME (Subject Matter Expert) for site and global projects Drive compliance with the site maintenance schedule through close collaboration with Production and QC teams Review and approve deviations, complaints, CAPAs, change controls and Out of Specification (OOS) / Out of Trend (OOT) investigations Maintain control of Quality documentation through the review and approval of SOPs, forms, logbooks, and templates Escalate serious quality matters to the Quality Leadership Team Support the QP in the withdrawal and recall process and reporting of quality defects to the DMRC About You: Degree or higher in relevant scientific area or equivalent experience in a pharmaceutical setting A strong background in Quality Assurance (4 years+) Aseptic or Sterile manufacturing background Good regulatory knowledge (GMP, Safety) Previous managerial experience Understanding of PrOFS Self-motivated
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Note
We generate this analysis from the job description. The listing may have changed since then, or the analysis may not be fully accurate — always check the original posting before applying.