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- Tasks: Lead and supervise the QC team, ensuring compliance with cGMP standards.
- Company: Join a dynamic sterile manufacturing organisation in North Wales.
- Benefits: Enjoy 25 holidays, early finishes on Fridays, and flexible working hours.
- Why this job: Advance your career in a supportive environment with impactful responsibilities.
- Qualifications: Bachelor's degree in a scientific discipline and 5 years of QC leadership experience required.
- Other info: Opportunity to develop internal SOPs and support method validation.
The predicted salary is between 36000 - 60000 £ per year.
I am currently recruiting for a QC Section Leader for a Sterile Manufacturing organisation based in North Wales. This is an exciting opportunity for an established leader within QC to progress their career.
Key responsibilities for the QC Section Leader:
- Lead and supervise the QC team ensuring deadlines are met within cGMP standards.
- Review any CAPAs, Change Controls and Deviations prior to QA approval.
- Write, review and develop internal SOPs for the most efficient process.
- Support method development, method validation and any equipment qualification.
- Lead batch release within the QC department.
Requirements for the QC Section Leader:
- Bachelor's degree in a Scientific discipline.
- Good understanding of GMP.
- 5 years working within QC with leadership experience.
Benefits for the QC Section Leader:
- 25 holidays per year + Bank Holidays.
- Christmas shutdown.
- Early finish on a Friday and flexible working hours.
To apply for the QC Section Leader or for more information, please contact Liam Shannon at Smart4Sciences.
QC Section Leader- Pharmaceuticals employer: Smart4Sciences
Contact Detail:
Smart4Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Section Leader- Pharmaceuticals
✨Tip Number 1
Familiarise yourself with the latest cGMP regulations and guidelines. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high-quality standards in the pharmaceutical industry.
✨Tip Number 2
Highlight your leadership experience in QC during networking events or industry meet-ups. Engaging with professionals in the field can provide valuable insights and potentially lead to referrals for the position.
✨Tip Number 3
Prepare to discuss specific examples of how you've successfully led a QC team in the past. Being able to articulate your achievements and challenges will set you apart from other candidates.
✨Tip Number 4
Stay updated on the latest trends in method development and validation within the pharmaceutical sector. Showing that you're proactive about continuous learning can impress potential employers.
We think you need these skills to ace QC Section Leader- Pharmaceuticals
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in Quality Control, especially any leadership roles. Emphasise your understanding of cGMP standards and relevant scientific qualifications.
Craft a Strong Cover Letter: Write a cover letter that specifically addresses the responsibilities mentioned in the job description. Discuss your experience with CAPAs, Change Controls, and your ability to lead a team effectively.
Showcase Relevant Experience: In your application, provide examples of how you've successfully led QC teams, managed method development, and ensured compliance with GMP standards. Use specific metrics or achievements where possible.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the QC field.
How to prepare for a job interview at Smart4Sciences
✨Showcase Your Leadership Skills
As a QC Section Leader, demonstrating your leadership experience is crucial. Be prepared to discuss specific examples of how you've successfully led a team, managed conflicts, and ensured that deadlines were met while adhering to cGMP standards.
✨Understand the Regulatory Environment
Make sure you have a solid grasp of Good Manufacturing Practices (GMP) and be ready to discuss how you've applied these principles in your previous roles. This will show your potential employer that you are well-versed in the necessary regulations for the pharmaceutical industry.
✨Prepare for Technical Questions
Expect questions related to CAPAs, Change Controls, and Deviations. Brush up on your knowledge of these processes and be ready to explain how you've handled them in the past, including any challenges you faced and how you overcame them.
✨Demonstrate Your Problem-Solving Skills
In the role of QC Section Leader, you'll need to support method development and validation. Be prepared to discuss specific instances where you've identified problems, developed solutions, and implemented changes that improved processes or outcomes.
