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- Tasks: Lead method validations and analytical tasks for drug products and raw materials.
- Company: Join Eurofins, a global leader in analytical testing across diverse industries.
- Benefits: Enjoy medical, dental, vision insurance, 401(k), and paid vacation.
- Why this job: Be part of a dynamic team making a real impact in pharmaceuticals.
- Qualifications: BS/MS in analytical chemistry with relevant industry experience required.
- Other info: Full-time role based in Lancaster, PA, Monday to Friday.
The predicted salary is between 36000 - 60000 £ per year.
Job Summary
Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, transfers, and verifications on APIs and finished products. Candidates should have expertise in method development and validation.
Responsibilities
- Apply GMP in all areas of responsibility.
- Perform analytical tasks for validation of methods used in testing drug products and raw materials, including HPLC, GC, UV/Vis, and dissolution.
- Interpret diverse analytical procedures.
- Conduct analytical investigations.
- Troubleshoot instrumentation and liaise with vendors.
- Train and mentor junior staff.
- Manage and discuss projects with clients.
Qualifications
- BS or MS degree in analytical chemistry or related field.
- BS with 4+ years, MS with 2+ years, or PhD with 1+ years of industry experience.
- 3-5 years of experience with LC chromatographic validation in a GMP environment.
- Excellent communication skills and attention to detail.
- Ability to work independently and in a team, with self-motivation and adaptability.
- Authorization to work in the U.S. without sponsorship.
Company Description
Eurofins Scientific is a global leader in analytical testing services across multiple industries, ensuring the safety and authenticity of products from food to pharmaceuticals. The network includes over 900 laboratories in 54 countries.
Additional Information
- Full-time position, Monday – Friday, 8:00 am – 4:00 pm.
- Location: Lancaster, PA, with candidates encouraged to apply if within commuting distance.
- Benefits include medical, dental, vision, life and disability insurance, 401(k), paid vacation and holidays.
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Senior Scientist, Small Molecule Method Development and Validation employer: Eurofins
Contact Detail:
Eurofins Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Scientist, Small Molecule Method Development and Validation
✨Tip Number 1
Familiarise yourself with the latest trends and technologies in analytical chemistry, particularly in HPLC, GC, and UV/Vis methods. This knowledge will not only help you during interviews but also demonstrate your commitment to staying current in the field.
✨Tip Number 2
Network with professionals in the industry, especially those who work at Eurofins or similar companies. Attend relevant conferences or webinars where you can meet potential colleagues and learn more about the company culture and expectations.
✨Tip Number 3
Prepare to discuss specific examples of your experience with method validation and troubleshooting instrumentation. Be ready to explain how you've applied GMP principles in your previous roles, as this will be crucial for the position.
✨Tip Number 4
Showcase your mentoring and training experience during the interview. Highlight any instances where you've successfully guided junior staff, as this aligns with the responsibilities of the Senior Scientist role.
We think you need these skills to ace Senior Scientist, Small Molecule Method Development and Validation
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in method development and validation, particularly with HPLC, GC, UV/Vis, and dissolution. Use specific examples to demonstrate your expertise and achievements in a GMP environment.
Craft a Strong Cover Letter: In your cover letter, express your passion for analytical chemistry and detail how your background aligns with the responsibilities of the Senior Scientist role. Mention your experience in training and mentoring junior staff, as well as your ability to manage projects and communicate effectively with clients.
Highlight Relevant Experience: When detailing your work history, focus on your 3-5 years of experience with LC chromatographic validation. Be specific about the types of projects you’ve worked on and any challenges you overcame, showcasing your problem-solving skills.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. Attention to detail is crucial in this field, and a polished application reflects your professionalism and commitment.
How to prepare for a job interview at Eurofins
✨Showcase Your Technical Expertise
Be prepared to discuss your experience with method development and validation in detail. Highlight specific projects where you applied techniques like HPLC, GC, and UV/Vis, and be ready to explain the challenges you faced and how you overcame them.
✨Demonstrate Your Understanding of GMP
Since the role requires applying Good Manufacturing Practices (GMP), make sure to articulate your knowledge of these regulations. Provide examples of how you've implemented GMP in previous roles, particularly in relation to analytical testing.
✨Prepare for Analytical Investigations
Expect questions about troubleshooting instrumentation and conducting analytical investigations. Think of scenarios where you identified issues in methods or equipment and how you resolved them, as this will showcase your problem-solving skills.
✨Emphasise Communication and Mentorship Skills
As the position involves training and mentoring junior staff, be ready to discuss your approach to leadership and communication. Share experiences where you successfully guided team members or collaborated with clients, highlighting your ability to work both independently and as part of a team.
