Analytical Chemical Process Development Scientist

Analytical Chemical Process Development Scientist

Full-Time 30000 - 40000 £ / year (est.) No working from home possible
Eurofins QTA Inc.

At a Glance

  • Tasks: Conduct analysis of pharmaceutical products using advanced techniques like HPLC, GC, and MS.
  • Company: Join Eurofins PSS, a diverse and innovative company committed to excellence.
  • Benefits: Enjoy competitive pay, health plans, life assurance, and perks like free parking.
  • Other info: Flexible working hours and opportunities for volunteering and global experiences.
  • Why this job: Make a real impact in pharmaceutical development while growing your career.
  • Qualifications: Degree in Chemistry or related field; experience with analytical techniques preferred.

The predicted salary is between 30000 - 40000 £ per year.

We’re proud to be an armed forces‑friendly place to work and welcome applications from reservists, armed forces veterans (including the wounded, injured and sick), as well as cadet instructors, and military spouses and partners. Unfortunately, we are unable to offer visa sponsorship for this role. This is a full‑time, permanent position working 35 hours per week flexibly between 07:00 – 19:00.

Eurofins PSS is recruiting for an analytical Scientist with a range of experiences from recent graduates to experienced scientists to provide on‑site analytical support as a Eurofins Managed PSS Scientist, based at the Bristol Myers Squibb Moreton facility in the Wirral. This position is a fully employed Analytical Scientist by Eurofins PSS, supporting services delivered to our client on their site. The role is not an employment with Bristol Myers Squibb and Bristol Myers Squibb does not manage the recruitment or employment terms for this position.

Job Responsibilities

  • You will perform routine and non‑routine analysis of pharmaceutical products using a range of analytical techniques (primarily HPLC, GC and MS).
  • You will support method development and proof of concept method validation for raw materials, intermediates and drug substances across a range of techniques.
  • You will review analytical data for GMP compliance and initiate or follow up on OOS results and action limits when required.
  • You will document data in accordance with current client policies and procedures and prepare/approve results for tests in which you are trained and deemed competent.
  • You will maintain productivity through agreed metrics (e.g., test numbers, cycle times) and support audits, method revisions, and testing of QC samples.
  • You will liaise with client representatives, provide updates to designated personnel, support continuous improvement initiatives, and work flexibly in line with business needs.

Qualifications and Experience

  • You will have a degree in Chemistry or a related scientific discipline; relevant experience may be considered in lieu of formal qualifications.
  • You’ll possess a sound, fundamental knowledge of Chemistry, with strong understanding of analytical & chromatographic techniques.
  • You have previous relevant experience within a pharmaceutical development environment and competence with techniques such as HPLC, GC, MS, IC, CAD and Karl Fisher.
  • You are experienced in working within a GMP environment, interpreting raw data, troubleshooting analytical or instrumental issues, and completing documentation accurately.
  • You are capable of working with electronic laboratory systems (ELNs, LIMS) and MS Office applications, and you can work proactively, independently, and as part of a team.
  • You are flexible in your approach, able to switch priorities at short notice, and motivated to contribute ideas to improve existing processes.

Benefits

  • Being part of a Reward and Recognition Scheme that recognises great work across our teams.
  • Holiday entitlement increases with service.
  • The option to opt into our Health Cash Plan, designed to help look after your everyday health and wellbeing.
  • Life Assurance from day one, providing cover of four times your annual salary.
  • Automatic enrolment into our Company Pension Plan after three months (with the flexibility to opt out if you choose).
  • Access to our Employee Assistance Programme, offering 24/7 confidential support for both personal and work‑related matters.
  • Opportunity to register interest in volunteering days, supporting employees who wish to do voluntary work during working hours as part of a wider community strategy.
  • Free on‑site car parking.
  • The opportunity to explore worldwide opportunities.
  • Everyone who joins our team also gets access to Perkbox, allowing you to save money all year round, with supermarket savings, days out, coffee, holidays and more.

We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability and everything else that makes employees of Eurofins companies unique.

Analytical Chemical Process Development Scientist employer: Eurofins QTA Inc.

Eurofins PSS is an exceptional employer, offering a supportive and inclusive work environment for Analytical Chemical Process Development Scientists at the Bristol Myers Squibb Moreton facility in the Wirral. With a strong focus on employee well-being, we provide a comprehensive benefits package, including a Reward and Recognition Scheme, health cash plan, life assurance, and opportunities for professional growth through volunteering and continuous improvement initiatives. Our commitment to diversity and flexibility ensures that every team member can thrive while contributing to meaningful projects in the pharmaceutical development sector.

Eurofins QTA Inc.

Contact Details:

Eurofins QTA Inc. Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Analytical Chemical Process Development Scientist

Tip Number 1

Network like a pro! Reach out to professionals in the pharmaceutical field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.

Tip Number 2

Prepare for interviews by practising common questions and showcasing your analytical skills. We recommend using the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your experience effectively.

Tip Number 3

Don’t forget to research Eurofins PSS and their work culture! Understanding their values and recent projects can help you tailor your responses during interviews and show that you’re genuinely interested in being part of the team.

Tip Number 4

Apply through our website for a smoother process! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to engage directly with us.

We think you need these skills to ace Analytical Chemical Process Development Scientist

HPLC
GC
MS
IC
CAD
Karl Fisher
GMP Compliance

Some tips for your application 🫡

Tailor Your CV:Make sure your CV is tailored to the role of Analytical Chemical Process Development Scientist. Highlight your relevant experience with analytical techniques like HPLC, GC, and MS, and don’t forget to mention any GMP experience you've got!

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 align with what we’re looking for. Be sure to mention your flexibility and teamwork spirit!

Showcase Your Achievements:When detailing your experience, focus on specific achievements rather than just duties. Did you improve a process or solve a tricky problem? We love to see how you’ve made an impact in previous roles!

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 keep track of it, so don’t miss out!

How to prepare for a job interview at Eurofins QTA Inc.

Know Your Analytical Techniques

Make sure you brush up on your knowledge of HPLC, GC, and MS. Be ready to discuss how you've used these techniques in past roles or projects, as well as any troubleshooting experiences you've had. This will show that you're not just familiar with the theory but also have practical experience.

Understand GMP Compliance

Since this role involves working in a GMP environment, it's crucial to understand what that entails. Familiarise yourself with the key principles of Good Manufacturing Practice and be prepared to discuss how you've ensured compliance in your previous work. This will demonstrate your commitment to quality and safety.

Prepare for Scenario Questions

Expect questions that ask you to solve hypothetical problems or describe how you would handle specific situations, especially related to method development or OOS results. Practising these scenarios can help you articulate your thought process and problem-solving skills effectively during the interview.

Show Your Team Spirit

This position requires collaboration with client representatives and team members. Be ready to share examples of how you've worked successfully in teams, contributed to continuous improvement initiatives, and adapted to changing priorities. Highlighting your flexibility and teamwork will make you stand out.