Details:
- Job Type: Permanent
- Job Status: Full-Time
- Location: Nationwide
- Date: 22 hours ago
Description:
Quality Assurance Officer
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.
The Employer
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
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.
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.
This is an excellent opportunity to apply your skills in a role that ensures patient safety and product excellence. If you are ready to take the next step in your QA career, apply today or contact us at (phone number removed) to discuss further