At a Glance
- Tasks: Lead a team in ensuring top-notch quality for pharmaceutical products.
- Company: Join one of the UK's largest and award-winning generic pharmaceutical companies.
- Benefits: Enjoy a competitive salary and benefits, with opportunities for skill development.
- Why this job: Be part of a dynamic team driving continuous improvement in a vital industry.
- Qualifications: BSc in Chemistry or related field, with QC experience and leadership skills.
- Other info: This role is site-based in North Wales, easily commutable from nearby towns.
The predicted salary is between 36000 - 60000 £ per year.
QC Section Leader
Permanent
North Wales – Site based, commutable from Deeside, Wrexham, Chester.
Competitive salary plus benefits
Are you an experienced QC Section Leader looking for the next step in your career? Are you looking to develop your skills whilst working for an award-winning Global Pharmaceutical company? A rare opportunity has arisen for a QC Section Leader to join one of the UK’s largest generic pharmaceutical companies.
Reporting in to the QC Manager, the QC Section Leader will be expected to:
- Manage the analytical testing of solid dose products using HPLC, GC, UV and IR.
- Lead a team of analysts and ensure that the release of our products meets the highest standards of quality and consistency.
- Ensure that all testing is carried out within the requirements of cGMP, ALCOA+, Health and Safety and COSHH.
- Critically review analytical data, and where specifications are met, approve products for further processing.
- Drive continuous improvement and ensure compliance with industry regulation and company policies.
The successful candidate for the QC Section Leader role will have:
- A BSc in Chemistry or Analytical Chemistry or relevant scientific degree, with significant experience in QC.
- Manage the workload of the QC solid dose team, including preparing weekly and daily work schedules.
- Previous experience in leading OOS/OOT investigations and deviations is essential.
- Previous experience in leading a team is preferred.
- Previous experience in representing the QC group at internal, customer and regulatory audits and liaising with the regulatory affairs department is essential.
- Experience in leading the analytical method transfer, verification and validation is preferred.
If you are an experienced QC Section Leader looking for a new challenge then please apply today!
Quality Control Team Lead employer: Kenton Black
Contact Detail:
Kenton Black Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Control Team Lead
✨Tip Number 1
Familiarise yourself with the specific analytical techniques mentioned in the job description, such as HPLC, GC, UV, and IR. Being able to discuss your hands-on experience with these methods during an interview will demonstrate your technical expertise and suitability for the role.
✨Tip Number 2
Highlight your leadership experience by preparing examples of how you've successfully managed a team in previous roles. Be ready to discuss specific challenges you faced and how you overcame them, as this will show your capability to lead the QC solid dose team effectively.
✨Tip Number 3
Research the company’s commitment to quality and compliance. Understanding their approach to cGMP, ALCOA+, and other regulations will allow you to align your answers with their values and demonstrate that you are a good fit for their culture.
✨Tip Number 4
Prepare to discuss your experience with OOS/OOT investigations and regulatory audits. Being able to articulate your role in these processes will show that you have the necessary experience to represent the QC group effectively and ensure compliance.
We think you need these skills to ace Quality Control Team Lead
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality control and leadership. Emphasise your BSc in Chemistry or Analytical Chemistry, and any specific achievements in managing QC teams or leading investigations.
Craft a Strong Cover Letter: Write a cover letter that directly addresses the job description. Mention your experience with HPLC, GC, UV, and IR analytical testing, and how you ensure compliance with cGMP and other regulations.
Highlight Leadership Experience: In your application, clearly outline your previous leadership roles. Discuss how you've managed workloads, prepared schedules, and led teams through audits and investigations.
Showcase Continuous Improvement Initiatives: Include examples of how you've driven continuous improvement in your previous roles. This could be through process enhancements, training initiatives, or successful project completions that align with industry standards.
How to prepare for a job interview at Kenton Black
✨Showcase Your Leadership Skills
As a QC Section Leader, you'll be managing a team. Be prepared to discuss your previous leadership experiences, how you motivate your team, and any challenges you've overcome in a supervisory role.
✨Demonstrate Technical Knowledge
Familiarise yourself with the analytical techniques mentioned in the job description, such as HPLC, GC, UV, and IR. Be ready to explain how you've used these methods in past roles and how they relate to quality control.
✨Prepare for Compliance Questions
Since compliance with cGMP, ALCOA+, and other regulations is crucial, expect questions on these topics. Brush up on your knowledge of industry standards and be ready to discuss how you've ensured compliance in your previous positions.
✨Highlight Continuous Improvement Initiatives
The role involves driving continuous improvement. Think of specific examples where you've implemented changes that enhanced quality or efficiency in your previous roles, and be prepared to share these during the interview.