QA Regulatory Manager and QP

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. 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. 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