Open role
QA Regulatory Manager and QP
- Aggregated by CV-Library
- Manchester, Greater Manchester
- Permanent
- Full Time
Job Description
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
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