At a Glance
- Tasks: Evaluate and test reference standard materials using advanced analytical techniques.
- Company: Join Eurofins, a leader in innovation and quality operations.
- Benefits: Enjoy competitive pay, health plans, and flexible working hours.
- Other info: Dynamic work environment with opportunities for growth and community involvement.
- Why this job: Make a real impact in the pharmaceutical industry while developing your skills.
- Qualifications: BSc or MSc in chemistry with hands-on analytical experience required.
The predicted salary is between 30000 - 40000 € per year.
This is a full time, 6 Month Fixed Term position working a flexible 36.5 hour week, Monday – Friday. As an Analytical Global Reference Standards Scientist, you will provide key analytical support to the Global Reference Standards (GRS) service area based within Quality Operations.
Job Responsibilities:
- Evaluate and test reference standard materials using a broad range of analytical techniques including HPLC, GC, titration, Karl Fischer, Sulphated Ash, Loss on Drying, and NMR interpretation.
- Produce Certificates of Analysis (CoAs) and associated technical documentation, providing robust scientific justification for the assignment of shelf life to reference standard materials.
- Act as system administrator for the Global Reference Standards (GRS) database and website, maintaining full accountability for material records, stock levels, retesting plans, and initiating procurement activities in line with lean principles and business demand.
- Process and manage internal and external reference standard orders via the GRS database, including allocation and dispensing of materials, and handling non‑standard or Pharmacopoeial requests through negotiation, sourcing, and coordination with procurement and storage teams.
- Work proactively with global and regional sourcing, CMOs, supply chain, technical stewardship teams, and other key stakeholders to ensure continuity of reference standard supply, assess analytical methodologies, and contribute to or lead improvement initiatives.
- Build strong relationships with sample dispatch teams and customers, respond to internal and external technical queries, drive productivity and efficiency through science and technology, challenge existing practices to add value, and support team development through collaboration, coaching, and mentoring.
Qualifications:
- BSc or MSc in a chemistry‑related discipline, with relevant experience gained within a pharmaceutical or regulated industry environment.
- Demonstrate a broad working knowledge of pharmaceutical analysis, with strong hands‑on experience in analytical chemistry and in‑depth expertise in HPLC.
- Experience in analytical method development, validation, and application, supported by a solid understanding of pharmaceutical manufacturing processes.
- Possess working knowledge of cGMP requirements and demonstrate the ability to operate effectively within a regulated quality environment.
- Digitally fluent, confident in using data‑driven and AI‑enabled approaches, basic scripting, or statistical tools to perform trend analysis, monitor method performance, identify early signals, and drive preventive actions and continuous improvement.
- Comfortable working with chromatography data systems (e.g. Empower) and LIMS/ELN platforms, using analytical data and system outputs to support robust scientific decision‑making.
Additional Information:
- Being part of a Reward and Recognition Scheme, recognising 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.
- Being able to register your interest in volunteering days, which are designed to support employees who wish to do voluntary work during working hours.
- Free on‑site car parking.
- The opportunity to explore worldwide opportunities.
- Access to Perkbox, allowing you to save money all year round.
What Happens Next:
As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and its requirements. This will give you the opportunity to see what working for Eurofins is really like and enable us to get to know your key skills and strengths.
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 Global Reference Standards Scientist (6 Month FTC) employer: Eurofins
At Eurofins, we pride ourselves on fostering a dynamic and inclusive work environment where innovation and collaboration thrive. As an Analytical Global Reference Standards Scientist, you will enjoy a flexible working schedule, comprehensive health benefits, and opportunities for professional growth, all while contributing to meaningful projects that impact global health. Our commitment to employee recognition and community engagement ensures that you will feel valued and supported throughout your career journey with us.
StudySmarter Expert Advice🤫
We think this is how you could land Analytical Global Reference Standards Scientist (6 Month FTC)
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for informational interviews. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for those interviews! Research the company and the role thoroughly, and practice answering common interview questions. We recommend using the STAR method (Situation, Task, Action, Result) to structure your responses and showcase your skills effectively.
✨Tip Number 3
Showcase your analytical skills! Since this role is all about analytical techniques, be ready to discuss your hands-on experience with HPLC, GC, and other methods. Bring examples of how you've tackled analytical challenges in the past.
✨Tip Number 4
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 Eurofins. Don’t miss out on this opportunity!
We think you need these skills to ace Analytical Global Reference Standards Scientist (6 Month FTC)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Analytical Global Reference Standards Scientist role. Highlight your relevant experience in analytical chemistry, especially with 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 explain why you're passionate about this role and how your background makes you a great fit. Don’t forget to mention any specific projects or achievements that relate to the job description.
Showcase Your Technical Skills:Since this role involves a lot of technical work, be sure to showcase your hands-on experience with analytical methods and data systems. Mention any familiarity with cGMP requirements and how you've used data-driven approaches in your 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 ensures you don’t miss out on any important updates from our team!
How to prepare for a job interview at Eurofins
✨Know Your Analytical Techniques
Make sure you brush up on your knowledge of analytical techniques like HPLC, GC, and NMR interpretation. Be ready to discuss how you've applied these methods in past roles, as well as any challenges you've faced and how you overcame them.
✨Showcase Your Regulatory Knowledge
Since this role involves working within a regulated environment, be prepared to talk about your understanding of cGMP requirements. Highlight any experiences you've had in ensuring compliance and how you’ve contributed to maintaining quality standards.
✨Demonstrate Digital Fluency
The job requires digital skills, so be ready to discuss your experience with data-driven approaches and tools like chromatography data systems or LIMS/ELN platforms. Share examples of how you've used these tools to drive improvements or solve problems.
✨Build Relationships
This role emphasises collaboration, so think about how you've built strong relationships in previous positions. Be ready to share specific examples of how you've worked with cross-functional teams or mentored others, showcasing your teamwork and communication skills.