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- Tasks: Join a dynamic team ensuring quality control in pharmaceutical production.
- Company: NextPharma, a leading European contract manufacturer in healthcare.
- Benefits: Full-time role with opportunities for growth and development.
- Why this job: Make a real impact in the pharmaceutical industry while working with cutting-edge technology.
- Qualifications: Relevant qualification in science and experience with analytical techniques.
- Other info: Fast-paced environment with a focus on teamwork and high-quality output.
The predicted salary is between 36000 - 60000 £ per year.
Location: Livingston, GB, EH53 0TH
Job Function: Quality Control
Anticipated Start Date: 23/03/2026
Job Type: Full-Time
Are you looking for an exciting professional challenge? We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,300 employees in Germany, France, Finland, UK and Norway. For us, the next step is always the one that matters most. Our fast pace drives us forward, fills our working environment with life and spurs our growth. Our winning formula for shared success: room for passion. Because we know that passion is the best medicine when it comes to excellent service around the world. Welcome to NextPharma.
Job Purpose: To support the production of both development and market finished products under GMP conditions in all areas of quality control and calibration.
Key responsibilities and accountabilities:
- Work as part of a team alongside Production and other analytical departments including development and stability.
- Actively involved in performing analytical activities to determine fitness for purpose of starting materials, intermediate and finished products.
- Technically competent in analytical activities (e.g., pharmacopeial wet chemistry, HPLC, GC, Dissolution) for QC testing of raw materials, packaging components and finished products.
- All activities to be performed under current cGMP, In house SOP’s and/or pharmacopoeia.
- Perform sampling of starting materials, packaging components and finished products.
- Perform cleaning verification analysis to assure suitability of Production equipment for subsequent use.
- Support calibration of key analytical equipment and measuring devices used in or on production equipment.
- Comply with company health and safety procedures.
Personality:
- Results oriented with a positive outlook and clear focus on high quality output.
- Solid planning and organizational ability; Reliable, tolerant, and dependable.
- Comfortable dealing with senior managers and customers; Enjoy working in a fast, stimulating environment.
- Goal-oriented; Able to work under pressure and meet deadlines.
- Excellent communication/presentation skills.
- Able to get on with others and be a team player but equally comfortable working independently.
Personal Situation: Flexible and able to work extended hours when required.
Specific Job Skills:
- Required: Relevant qualification, HNC/HND/Science Degree or Equivalent.
- An understanding of drug development and manufacturing processes.
- Demonstrated technical competence of the technical and practical skills involved in analytical activities to prescribed quality standards.
- Skilled in analytical techniques e.g., HPLC, Dissolution, Gas Chromatography, and wet chemistry techniques.
- Able to communicate well with others, both laboratory and non-laboratory based.
- Able to work with minimal supervision.
- Good understanding of quality control, SOP and GMP adherence.
- Desired: Have a broad knowledge with and experience of working within a cGMP/GLP environment.
- Experience of working within a pharmaceutical or biotechnology industry.
- Ability to work to key regulatory and compliance requirements.
- Experience of quality control within a pharmaceutical environment.
- Experience of Chromeleon software.
- Experience of data reporting and checking data within a QC environment.
- Understand and demonstrate a pragmatic approach to problem solving with GMP constraints.
Computer skills: Must be competent in the use of MS Office, particularly Excel and Word, e-mail and internet. Previous use of chromatographic acquisition software is desired but not essential.
Literacy and Numeracy: Must be competent in writing reports both for internal use and for customers. Must be competent in the interpretation of analytical data.
Business Presentation Skills: Must be an excellent face-to-face and telephone communicator.
Please note: Only candidates with continuing Right to Work in the UK will be considered.
NextPharma is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.
It's time for your next chapter: We look forward to receiving your application.
QC Analyst in Livingston employer: NextPharma
Contact Detail:
NextPharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Analyst in Livingston
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those who work at NextPharma. A friendly chat can open doors and give you insights that might just land you an interview.
✨Tip Number 2
Prepare for the interview by brushing up on your technical skills. Make sure you can confidently discuss HPLC, GC, and other analytical techniques. We want to see your passion for quality control shine through!
✨Tip Number 3
Showcase your teamwork skills! Be ready to share examples of how you've collaborated with others in fast-paced environments. We love candidates who can work well with both lab and non-lab teams.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining our team at NextPharma.
We think you need these skills to ace QC Analyst in Livingston
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the QC Analyst role. Highlight your relevant qualifications and experience, especially in analytical techniques like HPLC and GC. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for quality control and how you can contribute to our team. Be sure to mention any experience with GMP and SOPs, as these are key for us.
Showcase Your Communication Skills: Since communication is vital in this role, make sure to demonstrate your ability to convey complex information clearly. Whether it's in your CV or cover letter, we want to see that you can communicate effectively with both lab and non-lab folks.
Apply Through Our Website: We encourage you to apply directly 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 at NextPharma!
How to prepare for a job interview at NextPharma
✨Know Your Analytical Techniques
Brush up on your knowledge of analytical techniques like HPLC, GC, and wet chemistry. Be ready to discuss how you've applied these methods in previous roles or projects, as this will show your technical competence and understanding of quality control.
✨Familiarise Yourself with GMP Standards
Make sure you understand Good Manufacturing Practices (GMP) and how they apply to the role of a QC Analyst. Prepare examples of how you've adhered to these standards in past experiences, as this will demonstrate your commitment to quality and compliance.
✨Showcase Your Teamwork Skills
Since the role involves working closely with production and other departments, be prepared to share examples of successful teamwork. Highlight your ability to communicate effectively and collaborate under pressure, which is crucial in a fast-paced environment.
✨Prepare Questions for Your Interviewers
Think of insightful questions to ask your interviewers about the company culture, team dynamics, and specific challenges faced in the QC department. This shows your genuine interest in the role and helps you assess if it's the right fit for you.