At a Glance
- Tasks: Support validation projects and ensure compliance in a fast-paced GMP environment.
- Company: Leading pharmaceutical manufacturer with a focus on quality and innovation.
- Benefits: Highly competitive day rate, full-time contract, and opportunities for professional growth.
- Other info: Collaborative environment with a strong emphasis on continuous improvement.
- Why this job: Join a dynamic team and make a real impact on quality assurance in pharmaceuticals.
- Qualifications: Experience in QA and project management within a GMP setting.
The predicted salary is between 30000 - 40000 £ per year.
Contract Role (Highly Competitive Rate DOE)
Location: Cheshire
Sector: Pharmaceutical Manufacturing
Contract: Full time, on site
Our Client is seeking an experienced Senior QA Officer to join our Quality team on a contract basis, offering a highly attractive day rate for the right candidate. This role is ideal for a quality professional who thrives in a fast paced GMP environment and has proven experience managing project based work. This position plays a key role in supporting ongoing validation activities across the site. You will be responsible for ensuring that all data generated from validation work is accurately collated, assessed, and entered into the Pharmaceutical Quality Management System (QMS). Working closely with the QA Section Leader and wider Quality team, you will help maintain compliance, support continuous improvement, and ensure the smooth running of departmental operations.
Key Responsibilities
- Support ongoing validation projects, ensuring data is collected, reviewed, and entered into the QMS in a timely and compliant manner.
- Work collaboratively with cross functional teams to uphold GMP standards and maintain the Pharmaceutical Quality System.
- Review, approve, and manage quality documentation, ensuring accuracy and compliance with internal procedures.
- Assist with internal audits, risk management activities, investigations, and root cause analysis.
