At a Glance
- Tasks: Lead a team in analytical support, ensuring compliance and timely delivery of quality results.
- Company: Join Ethypharm, a dynamic pharmaceutical company focused on improving patient lives.
- Benefits: Enjoy 25-30 days holiday, private healthcare, and a bonus scheme.
- Other info: Flexible working arrangements and a commitment to diversity and inclusion.
- Why this job: Make a real impact in a collaborative environment while developing your skills.
- Qualifications: Degree in Chemistry or related field with experience in GMP-regulated labs.
The predicted salary is between 40000 - 50000 £ per year.
Location: Romford
Contract Type: Full-time, Permanent
Working Hours: Monday - Friday, 8:00am - 4:00pm, 37.5hrs per week.
Right to Work: Sponsorship not currently available
Under the guidance of the Quality Control Analytical Lead, the Analytical Support QC Supervisor leads/supervises the analytical support function within the QC laboratory, focusing on method development, validation, technical troubleshooting, and scientific support for product lifecycle activities. This role ensures the laboratory provides timely and expert analytical input to support manufacturing, quality investigations, and new product introductions, separate from routine batch release testing. The supervisor ensures all activities align with cGMP, regulatory expectations, and internal quality standards at our Romford site.
Your key responsibilities include:
- Supervise a team of analysts providing analytical support, ensuring work is prioritised, scheduled, and completed in a timely and compliant manner.
- Oversee method development, optimization, validation, and transfer activities in collaboration with internal stakeholders and external partners.
- Monitor team workload and performance, ensuring timelines and quality standards are met. Ensures compliance to all SOPs and maintains SOP training matrix.
- Provide expert troubleshooting support for analytical methods and instrumentation.
- Act as a technical subject matter expert for analytical methods and laboratory instrumentation. Demonstrate competency in most of test methods, analytical techniques and product preparation methods.
- Review and approve analytical protocols, reports, and technical documents in accordance with cGMP and regulatory requirements.
- Complete actions associated with CAPA, deviations and Change Control within agreed time schedule.
- Support continuous improvement initiatives within the QC department, including process optimisation and data integrity compliance.
About you
You will be an experienced QC professional with a strong background in a pharmaceutical laboratory environment. You'll have a good understanding of GMP and be confident working with analytical techniques and equipment. The role holder will be someone who takes pride in doing things properly, with a strong eye for detail and a practical approach to solving problems. You'll also be comfortable supporting others in the team, sharing your knowledge, and helping people develop. We're looking for someone who is organised, approachable, and able to manage changing priorities. You'll work well with others, communicate clearly, and bring a positive, committed approach to your work.
Basic skills and qualifications:
- Degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Substantial experience in a GMP-regulated QC laboratory within the pharmaceutical industry.
- Supervisory, mentoring, or team leadership experience.
- Strong technical knowledge of analytical instrumentation, such as HPLC, GC, FTIR, or UV.
- Good understanding of GMP, ICH guidelines, data integrity, and regulatory standards.
- Strong leadership, communication, organisation, and problem-solving skills.
What we offer you
- Holiday - 25 days rising to 30 with length of service plus bank holidays
- Holiday Buy/Sell - an opportunity to buy or sell up to an additional 5 days' holiday
- 5% Bonus - in addition to our competitive salaries, all our employees are entitled to join a discretionary bonus scheme (based on policy eligibility)
- Bravo Benefits Platform - offering a variety of discounts across well-being and lifestyle
- Salary Sacrifice scheme for Electric vehicles with Tusker (dependent on meeting policy eligibility)
- Private Healthcare for yourself and your family (if applicable) with an additional Medicash health cash plan
- Pension Scheme
About us
Ethypharm is a leading mid-sized international pharmaceutical company, with strong European roots, that manufactures and provides essential medicines, with a focus on hospital care, central nervous system (severe pain and addiction) and internal medicine. Ethypharm has 1,700 employees dedicated to its various pharmaceutical activities, of which 1400 are in industrial operations. Our six production sites located in France, the UK, Spain, and China have expertise in injectables and complex oral solid forms. At Ethypharm, you will be a part of a team dedicated and committed to improving patients' lives. Our Romford facility located 20 miles from the centre of London, consists of over 6700 square metres of a high-quality, modern pharmaceutical facility where we mix, fill, sterilise, inspect, pack, and label a wide range of medicines.
Why Ethypharm?
We provide a workplace which is one of collaboration, teamwork and innovation. We are all different and we embrace this uniqueness in each and every one of our employees. Our commitment to you is that we want to help you unleash your full potential by supporting your training and development. We want you to be the best that you can be. At Ethypharm we recognise the value of diversity in the workplace and provide equal opportunities for all. We are always open to discussing flexible working arrangements where this meets with the needs of our business.
QC Supervisor - Analytical Support employer: Ethypharm
Ethypharm is an excellent employer that fosters a collaborative and innovative work culture, particularly at our Romford facility, where you will be part of a dedicated team focused on improving patients' lives. We offer competitive benefits including generous holiday allowances, private healthcare, and a commitment to employee development, ensuring you have the support needed to grow in your career. With a strong emphasis on diversity and flexible working arrangements, Ethypharm provides a rewarding environment for those looking to make a meaningful impact in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land QC Supervisor - Analytical Support
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work at Ethypharm or similar companies. A friendly chat can sometimes lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge. Make sure you can confidently discuss analytical techniques and instrumentation, as well as your experience with GMP regulations. We want to see that you're not just a fit on paper but also in practice!
✨Tip Number 3
Showcase your leadership skills! If you've supervised teams before, be ready to share specific examples of how you managed workloads and supported your colleagues. We love to see candidates who can inspire and guide others.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at Ethypharm.
We think you need these skills to ace QC Supervisor - Analytical Support
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the QC Supervisor role. Highlight your experience in analytical support, method development, and any supervisory roles you've held. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your skills can contribute to our team. Be sure to mention your understanding of GMP and your problem-solving approach.
Showcase Your Technical Skills:Don’t forget to highlight your technical knowledge of analytical instrumentation like HPLC or GC. We’re keen on seeing how you’ve applied these skills in previous roles, so give us some solid examples!
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!
How to prepare for a job interview at Ethypharm
✨Know Your Analytical Techniques
Make sure you brush up on your knowledge of analytical techniques like HPLC, GC, and FTIR. Be ready to discuss how you've used these methods in past roles, as well as any troubleshooting experiences you've had. This will show that you're not just familiar with the equipment but can also handle challenges effectively.
✨Demonstrate Leadership Skills
As a QC Supervisor, you'll be leading a team, so it's crucial to highlight your supervisory experience. Prepare examples of how you've mentored others or managed team dynamics in previous positions. This will help the interviewers see you as a strong candidate who can inspire and guide a team.
✨Understand cGMP and Regulatory Standards
Familiarise yourself with current Good Manufacturing Practices (cGMP) and relevant regulatory guidelines. Be prepared to discuss how you've ensured compliance in your previous roles. This knowledge is essential for the role and will demonstrate your commitment to quality and safety.
✨Showcase Problem-Solving Abilities
Think of specific instances where you've successfully solved problems in a laboratory setting. Whether it was optimising a method or addressing a deviation, having concrete examples will illustrate your practical approach and attention to detail, which are key traits for this position.
