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- Tasks: Supervise QC operations, mentor analysts, and ensure compliance in a dynamic lab environment.
- Company: Leading GMP pharmaceutical manufacturer known for quality and innovation.
- Benefits: Competitive day rate and a 12-month leadership opportunity.
- Why this job: Join a vital QC function and enhance your management skills in a respected environment.
- Qualifications: Experience in GMP QC, supervisory skills, and a degree in a scientific discipline.
- Other info: Collaborative team atmosphere with strong development exposure.
The predicted salary is between 36000 - 60000 £ per year.
You will be joining a leading GMP regulated pharmaceutical and biotech manufacturer with a strong reputation for quality, innovation, and patient focused operations. The organisation plays a key role in delivering high quality products to global markets and is committed to maintaining the highest standards of compliance, safety, and technical excellence. As part of their Quality Control function, you will be joining a collaborative and high performing team during a critical period of maternity cover.
As the QC Supervisor, you will oversee day to day QC operations across multiple laboratory work streams, ensuring documentation, testing activities, and compliance standards are consistently met. You will supervise and mentor analysts, manage workflow allocation, and ensure key QC processes remain efficient, compliant, and inspection ready. Your role will span documentation oversight, data integrity, QMS activities, audit support, GMP coaching, and routine laboratory support across QC areas such as chemistry, stability, raw materials, and microbiology. You will work closely with cross functional teams including QA, Production and Supply Chain, to resolve issues and maintain seamless operational performance.
What you’ll need to succeed:
- Significant experience working within a GMP QC environment
- Previous experience supervising, mentoring, or leading junior analysts
- Strong working knowledge of QMS, documentation control and data integrity principles
- Experience supporting deviations, CAPAs, change controls or investigation activities
- Excellent organisational, communication and report writing skills
- Confident in collaborating across departments and communicating with stakeholders
- Proficiency with QC software and electronic QMS tools
- A degree in a scientific discipline or equivalent QC experience
What you’ll get in return:
- A competitive day rate
- A 12‑month opportunity to step into a leadership-level QC role
- The chance to strengthen your management and supervisory experience
- A key role supporting a vital QC function during an important period for the business
- The ability to work within a respected GMP pharmaceutical environment with strong development exposure
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.
QC Supervisor employer: HAYS Specialist Recruitment
Contact Detail:
HAYS Specialist Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Supervisor
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical and biotech sectors. Attend industry events or webinars to meet potential employers and get your name out there.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP regulations and QC processes. Be ready to discuss your experience with documentation control and data integrity, as these are key areas for the QC Supervisor role.
✨Tip Number 3
Showcase your leadership skills! Think of examples where you've mentored or supervised others in a QC environment. This will demonstrate your ability to manage workflow and support junior analysts effectively.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate individuals to join our team.
We think you need these skills to ace QC Supervisor
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in GMP QC environments and any supervisory roles you've held. We want to see how your skills match the job description, so don’t be shy about showcasing your relevant achievements!
Showcase Your Communication Skills: Since this role involves collaboration across departments, it’s crucial to demonstrate your excellent communication abilities. Use examples in your application that show how you’ve effectively communicated with stakeholders or led teams.
Highlight Your QMS Knowledge: We’re looking for someone with a strong understanding of Quality Management Systems. Be sure to mention any specific tools or software you’ve used, and how you’ve applied data integrity principles in your previous roles.
Apply Through Our Website: To make sure your application gets the attention it deserves, apply directly through our website. It’s the best way for us to keep track of your application and ensure you’re considered for this exciting opportunity!
How to prepare for a job interview at HAYS Specialist Recruitment
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) before the interview. Be ready to discuss how you've applied these principles in your previous roles, especially in a QC environment. This will show that you understand the importance of compliance and quality in the pharmaceutical industry.
✨Showcase Your Leadership Skills
As a QC Supervisor, you'll be expected to lead and mentor junior analysts. Prepare examples of how you've successfully supervised teams or managed workflows in the past. Highlight any specific challenges you faced and how you overcame them to demonstrate your leadership capabilities.
✨Familiarise Yourself with QMS Tools
Since proficiency with QC software and electronic QMS tools is crucial for this role, make sure you're comfortable discussing the systems you've used. If possible, research the specific tools the company uses and be prepared to explain how your experience aligns with their requirements.
✨Prepare for Cross-Departmental Collaboration
Collaboration is key in this role, so think about times when you've worked with other departments like QA or Production. Be ready to share examples of how you resolved issues through teamwork and effective communication. This will show that you can maintain seamless operational performance across functions.
