Principal Scientist, Drug Product Analytical Development at Eurofins

Groton, Connecticut, United States -

Full Time

Start Date

Immediate

Expiry Date

11 Jan, 26

Salary

0.0

Posted On

13 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Chemistry, Pharmaceutical R&D, Chromatography, Mass Spectrometry, Dissolution, Spectroscopy, NMR, Data Analysis, Regulatory Requirements, Method Transfer, Scientific Software, Data Systems, Modeling Tools, Leadership, Problem-Solving, Mentoring

Industry

Medical and Diagnostic Laboratories

Description

Company Description The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you’re looking for a rewarding career, apply with us today! Job Description Work in a GLP or GMP environment with appropriate documentation and safety practices Lead the development and execution of analytical strategies for new drug product candidates Plan, direct, and review laboratory work, including method development, validation, and transfer Design and interpret stability studies to understand degradation mechanisms and support shelf-life assignments. Develop impurity control strategies aligned with regulatory expectations. Collaborate with formulations, process and regulatory teams to ensure seamless pharmaceutical drug development Collaborate with colleagues to identify appropriate analytical approaches, including use of computational predictive tools, modeling software and data visualization tools where appropriate Critically review and interpret scientific data to derive clear conclusions and provide direction for future work Mentor and guide junior scientists in analytical techniques and data interpretation. Evaluate and implement new strategies as needed, e.g. working with external partners Communicate results and conclusions through various media including presentations and technical reports Author relevant sections of the quality modules of regulatory submissions Qualifications Ph.D. in Analytical Chemistry or related field, with 5-7+ years of pharmaceutical R&D experience, or B.S./M.S. with 15+ years of pharmaceutical R&D experience required Authorization to work in the United States indefinitely without restriction or sponsorship Proven expertise in a broad range of analytical techniques, e.g,. chromatography, mass spectrometry, dissolution, spectroscopy, NMR, and data analysis Strong understanding of regulatory requirements and experience with regulatory filings Experience with method transfer and working with external partners Proficiency in scientific software, data systems, and modeling tools Demonstrated leadership, problem-solving, and mentoring capabilities Desired Qualifications: Experience with mathematical modeling or coding Candidates currently living within a commutable distance of Groton, CT are encouraged to apply Additional Information Position is full-time, Monday-Friday, 8:00 am - 5:00 pm. Excellent full-time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Responsibilities

Lead the development and execution of analytical strategies for new drug product candidates while planning, directing, and reviewing laboratory work. Collaborate with various teams to ensure seamless pharmaceutical drug development and mentor junior scientists.