At a Glance
- Tasks: Manage controlled documents and provide admin support for quality processes in pharma.
- Company: Join a leading pharmaceutical company in Birmingham with a focus on bespoke medicines.
- Benefits: Temp to perm role with opportunities for career growth and development.
- Other info: Ideal for those passionate about quality assurance in a regulated environment.
- Why this job: Be part of a team ensuring high-quality standards in innovative medicinal products.
- Qualifications: Degree in a scientific or quality-related field and strong Excel skills required.
The predicted salary is between 30000 - 40000 £ per year.
Talentmark are recruiting for a QA Administrator to join a pharmaceutical company, based in Birmingham, on a permanent basis. Our client is a Pharma manufacturing company that produces, imports, and distributes bespoke medicines (Specials) and CBPMs (Cannabis-Based Products for Medicinal Use).
Responsibilities include:
- 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.
Requirements:
- Degree in scientific, pharmaceutical or quality-related discipline.
- Previous administration experience in an office or documentation-focused role.
- Strong command in Microsoft Excel.
- Experience in a GMP, pharmaceutical, specials or other regulated environment.
- Knowledge of Specials Manufacturing regulatory requirements and MHRA guidance.
Quality Assurance Administrator - Temp to Perm in Birmingham employer: Talentmark
Join a leading pharmaceutical company in Birmingham that values quality and compliance, offering a supportive work culture where your contributions directly impact the production of bespoke medicines. With a focus on employee growth, you will have access to ongoing training and development opportunities, ensuring you thrive in your role as a Quality Assurance Administrator. Enjoy the unique advantage of working in a dynamic environment that prioritises innovation and adherence to the highest regulatory standards.
