Your new company

Your new role

• Compliance: Ensuring the site adheres to all relevant GMP regulations and guidelines, including those related to production, quality control, and facilities.
• Personnel Management: Supervising and coordinating site staff, ensuring they are trained and competent in their roles.
• Record Keeping: Maintaining accurate and up-to-date records of all production activities, testing, and quality control procedures.
• Process Monitoring: Implementing and monitoring processes to ensure they are consistent and in compliance with GMP standards.
• Problem-Solving: Identifying and resolving any deviations or issues that arise during production or quality control.

What you'll need to succeed

• Experience in a pharmaceutical manufacturing environment.
• Strong knowledge of GMP regulations and guidelines.
• Excellent leadership and communication skills.
• Ability to manage and supervise personnel effectively.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.