QA Supervisor - Pharmaceutical Sector (North West)Are you a quality‑driven professional with a passion for leadership and compliance?... Read more
QA Supervisor - Pharmaceutical Sector (North West)
Are you a quality‑driven professional with a passion for leadership and compliance? A well‑established pharmaceutical group is looking for a QA Supervisor to join their team and play a pivotal role in maintaining regulatory standards and driving continuous improvement.
In this role, you'll lead a team of QA Specialists, ensuring the Quality Management System (QMS) is inspection‑ready at all times. You'll oversee deviations, CAPAs, change controls, and validation activities, while supporting audits and mentoring your team to deliver excellence. This is a fantastic opportunity to combine hands‑on technical expertise with people management, making a real impact on quality culture and operational success.
What you'll be doing:
Leading and developing QA Specialists, motivating team performance
Ensuring timely completion of QMS activities and audit readiness
Reviewing and approving deviations, CAPAs, and change controls
Supporting internal and external audits (MHRA, customer, supplier)
Driving continuous improvement across QA operations
What we're looking for:
Solid validation experience, (quipment validation/manufacturing validation/process validation) - IQ/OQ/PQStrong knowledge of cGMP and regulatory compliance
Experience managing QA teams and quality systems
Excellent communication, organisation, and problem‑solving skills
Confident decision‑maker with high attention to detail
Why apply? This is a chance to step into a leadership role where your technical skills and people management abilities will directly shape the success of a growing pharmaceutical business.
If you're ready to take the next step in your QA career, apply today or reach out for a confidential chat.
Are you an organised, detail-focused Quality professional looking to develop your career within a fast-paced pharmaceutical environment? Smart4... Read more
Are you an organised, detail-focused Quality professional looking to develop your career within a fast-paced pharmaceutical environment? Smart4 Sciences supporting a well-established pharmaceutical group in the North West who are looking to add a Quality Assurance Assistant to their Quality team
In this role, you'll work closely with Production, Quality, Regulatory and QP teams to ensure all batches are produced to GMP standards, on time, and to the highest level of accuracy. You'll play a key role in the production rooms - conducting in-process checks, signing jobs on/off, completing batch documentation, identifying deviations, and supporting the training and performance of packing teams.
Key Responsibilities
Conduct quality checks in production rooms in line with SOPs and GMPBrief room teams on licence-specific packing requirementsPerform regular in-process checks and provide cover during breaksInspect, sample and investigate any factors impacting qualityEvaluate and sign off batch records for QP reviewReport deviations and complete rework and deviation documentationEnsure correct reconciliation and room clearancesMaintain accurate stock movements on the intranetTrain new staff and lead by example in GMP compliance
What We're Looking For
Experience in pharmaceutical repackaging and/or quality checkingStrong understanding of GMP principlesConfident communicator who can influence without hierarchyExcellent attention to detail, organisation and problem-solving skillsProficient in Microsoft Word, Excel and OutlookAbility to work under pressure, meet deadlines and support team performance
Personal Attributes
Accurate, efficient and adaptableStrong team player with a customer-focused mindsetAble to work independently and use initiativeProfessional, friendly, and keen to learn quickly
If this sounds like the right role for you please apply now, or reach out for a confidential chat
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