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- Tasks: Ensure compliance with cGMP during manufacturing and testing operations.
- Company: Join a global leader in generics and biopharmaceuticals.
- Benefits: Earn £34.94 per hour with a 12-month contract.
- Why this job: Make a real impact on patient lives through quality assurance.
- Qualifications: Degree in Science and registration as a Qualified Person required.
- Other info: Dynamic role with opportunities for professional growth.
CK Group are recruiting for a Quality Qualified Person to join a global pharmaceutical company on a contract basis for 12 months.
Salary: £34.94 per hour PAYE
Quality Qualified Person role:
- To ensure the principles and guidelines of cGMP have been met during manufacturing, packaging and testing operations.
- To verify all batch related documentation is compliant with the requirements of the regulatory authorities.
- To review and certify batches in line with business shipment schedules.
- To ensure Product Licences (Marketing Authorisations), ANDAs, Manufacturer's Licence, Technical Agreements, CE Certification requirements have been met to ensure compliance.
- To ensure planned changes or deviations are supported by appropriate sampling, inspection, testing and checks to ensure compliance with the requirements of the regulatory authorities.
Your Background:
- Qualified to Degree level or equivalent in Science.
- Membership of appropriate professional body.
- Registration as a Qualified Person, with acceptability to the Licensing Authority.
- Significant experience in a senior Quality role with experience as a Quality Leader in a modern manufacturing environment within the pharmaceutical industry desirable.
- The ability to work effectively with peers, partners and others, to positively impact performance.
Company: Our client's aim is to be a global leader in generics and biopharmaceuticals, improving the lives of patients across the world.
Location: This role is based at our client's site in Runcorn.
Apply: For more information, or to apply for this Quality Qualified Person role please contact the Key Accounts Team or email. Please quote reference.
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. It is essential that applicants hold entitlement to work in the UK.
Quality Qualified Person in Runcorn employer: CK Group- Science, Clinical and Technical
Contact Detail:
CK Group- Science, Clinical and Technical Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Qualified Person in Runcorn
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the hunt for a Quality Qualified Person role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on cGMP principles and relevant regulations. We want you to be able to showcase your expertise confidently, so practice answering common interview questions related to quality assurance and compliance.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Check out our website for opportunities at leading firms in the pharmaceutical sector, and tailor your approach to each one.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. It shows your enthusiasm for the role and gives you another chance to highlight why you’re the perfect fit for the Quality Qualified Person position.
We think you need these skills to ace Quality Qualified Person in Runcorn
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in quality roles, especially in the pharmaceutical industry. We want to see how your background aligns with the Quality Qualified Person role, so don’t be shy about showcasing your achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for this position. We love seeing enthusiasm and a clear understanding of the role, so let your personality come through while keeping it professional.
Showcase Your Qualifications: Since this role requires specific qualifications, make sure to clearly list your degree and any relevant certifications. We need to know you’re registered as a Qualified Person and that you meet the regulatory requirements, so don’t leave that out!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications and ensures you don’t miss any important updates. Plus, it’s super easy – just follow the prompts!
How to prepare for a job interview at CK Group- Science, Clinical and Technical
✨Know Your cGMP Inside Out
Make sure you brush up on the principles and guidelines of current Good Manufacturing Practice (cGMP). Be ready to discuss how you've applied these in your previous roles, especially in manufacturing, packaging, and testing operations.
✨Familiarise Yourself with Regulatory Requirements
Understand the key regulatory authorities and their requirements for Product Licences, ANDAs, and CE Certification. Prepare examples of how you've ensured compliance in past positions, as this will show your expertise and attention to detail.
✨Highlight Your Leadership Experience
Since the role requires significant experience in a senior Quality position, be prepared to share specific instances where you've led a team or project. Discuss how you positively impacted performance and compliance in a modern manufacturing environment.
✨Prepare Questions for Them
Interviews are a two-way street! Think of insightful questions about the company's approach to quality assurance and how they handle deviations or changes. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
