At a Glance
- Tasks: Manage controlled documents and support quality processes in a pharmaceutical setting.
- Company: Join a leading pharmaceutical company in Birmingham with a focus on bespoke medicines.
- Benefits: Competitive salary, career growth, and a chance to make a difference in healthcare.
- Other info: Dynamic work environment with opportunities for professional development.
- Why this job: Be part of a team ensuring high-quality standards in innovative medicinal products.
- Qualifications: Degree in a relevant field and experience in administration or documentation.
The predicted salary is between 29000 - 29000 £ per year.
Talentmark are recruiting for a QA Administrator to join a pharmaceutical company, based in Birmingham, on a permanent basis. The salary is around £27,000-£29,000 per annum.
The Company: Our client is a Pharma manufacturing company who produce, import, and distribute bespoke medicines (Specials), and CBPMs (Cannabis-Based Products for Medicinal Use).
Your main duties will be:
- Manage the lifecycle of all controlled documents within the paper-based QMS (SOPs, forms, master documents, batch records, policies and specifications).
- Provide administrative support for deviations, NCs, CAPAs, change controls, complaints and incident reports.
- Ensure document activities comply with EU GMP (as applicable to Specials), MHRA expectations, and internal quality procedures.
- Work closely with Production, QC and QA teams to ensure correct and timely use of controlled documents.
- Design and execute method validation/verification, method transfers and robustness studies as required.
Your Background (Essential):
- Degree in scientific, pharmaceutical or quality-related discipline.
- Previous administration experience in an office or documentation-focused role.
- Strong command in Microsoft Excel.
Your Background (Desirable):
- Familiarity with core GMP documentation.
- Experience in a GMP, pharmaceutical, specials or other regulated environment.
- Knowledge of Specials Manufacturing regulatory requirements and MHRA guidance.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 193744 in all correspondence.
If this position isn’t suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (Talentmark) and follow us to see our latest jobs and company news.
Quality Assurance Administrator in Birmingham employer: Talentmark
As a Quality Assurance Administrator at our Birmingham-based pharmaceutical company, you will be part of a dynamic team dedicated to producing bespoke medicines and cannabis-based products for medicinal use. We pride ourselves on fostering a collaborative work culture that values employee growth through continuous training and development opportunities, alongside competitive salaries and benefits. Join us to make a meaningful impact in the healthcare sector while enjoying the unique advantages of working in a vibrant city known for its rich history and innovation.