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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 in Norfolk employer: HAYS Specialist Recruitment
Contact Detail:
HAYS Specialist Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Supervisor in Norfolk
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical and biotech sectors. Attend industry events or webinars, and don’t be shy about introducing yourself to potential employers. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their commitment to quality and compliance, and think of examples from your experience that align with their values. We want you to shine and show them why you’re the perfect fit for their QC team!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. We can help you with common questions related to QC operations and leadership, so you’re ready to impress when it counts.
✨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 on the lookout for talented individuals like you to join our collaborative teams in the QC space. Let’s get you that job!
We think you need these skills to ace QC Supervisor in Norfolk
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in a GMP QC environment. We want to see how your skills match the job description, so don’t be shy about showcasing your relevant achievements!
Showcase Leadership Skills: Since this role involves supervising and mentoring, it’s crucial to emphasise any previous leadership experience. We love to see examples of how you've guided teams or improved processes in your past roles.
Be Clear and Concise: When writing your application, clarity is key! Use straightforward language and structure your thoughts logically. We appreciate well-organised applications that are easy to read.
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
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 familiar with the specific systems used by the company. If possible, research their software and be prepared to discuss your experience with similar tools during the interview.
✨Prepare for Cross-Departmental Collaboration
Collaboration is key in this role, so think about times when you've worked with other departments like QA, Production, or Supply Chain. Be ready to share how you resolved issues and maintained operational performance, as this will demonstrate your ability to work effectively across teams.
