RBW Consulting
QA Regulatory Manager (Trainee / Newly Qualified QP)
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QA Regulatory Manager (Trainee / Newly Qualified QP)
Site-based with flexibility for some remote working in the long term
Location
Can be based at any UK site: Guildford, South West London, Sheffield, Preston, Stoke-on-Trent or Manchester
Are you currently working towards QP status or recently qualified and looking for an opportunity that offers genuine career development? Our client, a growing sterile pharmaceutical manufacturer, is seeking a QA Regulatory Manager to join their Quality team.
This unique position has been designed for a Trainee QP or Newly Qualified QP, providing the opportunity to complete your QP training while gaining valuable experience across Quality Assurance, Regulatory Affairs and QP-related activities. Reporting to the Head of Quality, you will play a key role in supporting regulatory compliance, quality systems and the manufacture of sterile pharmaceutical products across multiple UK sites.
What You'll Do
- Support QP activities and gain exposure to batch certification processes.
- Assist with regulatory projects, licence maintenance, variations and regulatory submissions.
- Contribute to IMP and commercial product regulatory activities, including quality documentation and compliance support.
- Support quality systems including deviations, CAPAs, change controls and risk assessments.
- Work closely with Quality, Manufacturing, QC and Development teams to ensure GMP compliance.
- Assist with inspections, audits and interactions with regulatory authorities.
- Review and approve quality documentation including SOPs, protocols and reports.
- Develop knowledge and expertise in sterile manufacturing, aseptic processing and regulatory requirements.
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What You'll Bring
- Working towards QP eligibility, currently enrolled on a QP programme, or recently qualified as a QP.
- Experience within a GMP-regulated pharmaceutical environment.
- Exposure to QA, Compliance, Regulatory Affairs or Quality Systems activities.
- Understanding of UK/EU GMP requirements.
- Experience within sterile, aseptic, biologics or pharmaceutical manufacturing environments would be advantageous.
- Strong communication skills and the ability to work collaboratively across functions.
- Scientific degree or equivalent qualification.
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Why Apply?
This is an excellent opportunity to accelerate your QP journey within a supportive and expanding pharmaceutical business. You'll gain exposure to both regulatory affairs and quality leadership activities while working alongside experienced QPs in a complex sterile manufacturing environment. The role offers broad development opportunities, genuine career progression and the chance to make a meaningful impact across multiple UK sites.
Keywords
QP, Qualified Person, Trainee QP, Newly Qualified QP, QA, Quality Assurance, Regulatory Affairs, RA, GMP, Sterile Manufacturing, Aseptic, Pharmaceutical, IMP, Clinical Trials, Compliance, Quality Systems, CAPA, Change Control, GDP, MHRA
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