At a Glance
- Tasks: Ensure compliance with quality standards and manage audits in a dynamic pharmaceutical environment.
- Company: Join a leading pharmaceutical company committed to innovation and high-quality products.
- Benefits: Gain valuable experience, work in a supportive team, and develop your career in a fast-paced industry.
- Other info: Full-time role with a collaborative culture and opportunities for continuous improvement.
- Why this job: Make a real impact on product quality and safety while growing your expertise in the field.
- Qualifications: BSc in Pharmaceutical Sciences and at least 6 months' experience in GMP.
The predicted salary is between 30000 - 40000 £ per year.
- Quality Assurance Officer - Pharma
- Birmingham
We are seeking a highly motivated and detail-oriented Quality Assurance Officer to join a growing pharmaceutical business dedicated to excellence in GMP & GDP compliance.
This is a fantastic opportunity for someone looking to develop their career in a fast-paced, regulated environment.
If you have a passion for quality, a strong scientific background, and the ability to work to rigorous standards, this role could be perfect for you.
Company Overview
Our client is a well-established pharmaceutical organisation recognised for delivering high-quality products and ensuring compliance with stringent industry regulations.
They pride themselves on their commitment to innovation, safety, and consistent delivery to their customers.
Joining this team means working with a company that values integrity, collaboration, and continuous improvement, offering an environment where your skills will make a real impact.
Qualifications & Experience
- BSc in Pharmaceutical Sciences (or related discipline).
- Minimum of 6 months' experience in a GMP pharmaceutical facility.
- Knowledge of Quality Management Systems, regulatory guidelines, and validation protocols.
Responsibilities include
As a Quality Assurance Officer, you will ensure compliance with statutory requirements and the company's Quality Management System, delivering best practice across operations.
Key duties include
- Establish and maintain the Quality Management System.
- Investigate non-conformances and implement corrective actions.
- Approve specifications for raw materials and finished products.
- Manage supplier audits and approve starting material suppliers.
- Oversee QC testing, validation of equipment and processes.
- Release raw materials and ensure TSE/BSE compliance certification.
- Conduct internal audits, manage CAPA systems, and handle change control processes.
- Provide guidance and training to ensure GMP compliance across teams.
- Experience & Qualifications
- Strong understanding of GMP, GDP and quality principles.
- Familiarity with documentation such as SOPs, validation protocols, and batch records.
- Ability to perform internal audits, supplier evaluations, and QC oversight.
Skills / Technical Competencies
- Strong understanding of GMP, GDP and quality principles.
- Familiarity with documentation such as SOPs, validation protocols, and batch records.
- Ability to perform internal audits, supplier evaluations, and QC oversight.
Nice to Haves
- Experience with HVAC systems and risk assessment protocols.
- Knowledge of environmental monitoring and calibration procedures.
- Familiarity with MHRA guidelines and product recall processes.
- On-site full time – 10am – 7pm - Monday to Friday
