Company Description
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, 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, a place to call home, apply with us today!
Job Description
Eurofins is seeking a highly skilled, passionate, and motivated scientist to join our client Analytical Development team to support testing non-GMP samples for development studies such as comparability assessments, process development, stability, product, and process characterization.The Analytical Development team is responsible for developing and implementing new analytical methods, as well as optimizing and improving current methods for the characterization of raw materials, RNA drug substances, and LNP products and programs at various development stages.
- Provide testing support for a variety of purposes, including release and stability testing, product characterization, high-throughput analysis, and characterization of complex raw materials.
- Collect, process, and analyze experimental data, ensure accurate and timely documentation in electronic laboratory notebook.
- Review, interpret, and present data within the analytical team and cross-functionally.
- Author, review, and revise technical source documents to support phase-appropriate comparability.
- Provide technical oversight to guide analytical/QC investigations, as needed.
- Actively collaborate with internal and external process development and quality teams.
- Train and mentor junior team members as needed.
Qualifications
Basic Minimum Qualifications:
- B.S. in Analytical Chemistry, Biochemistry, Biophysics, or related field with 3-4 years of biotech industry experience utilizing FTIR, HPLC/UPLC, and LCMS or M.S. degree with 1-2 year of biotech industry experience utilizing FTIR, HPLC/UPLC, and LCMS
- Experience working with various biophysical instrumentation such as HPLC/UPLC (various detectors) and capillary electrophoresis (CE)
- Strong technical background on analytical methodologies using IP-RP, IEX, and AEX.
- Proficiency with instrumentation such as Waters and Agilent LCs.
- Proficiency with software systems such as OpenLab, Empower, and ELN (Benchling is a plus).
- Previous experience developing methods for mRNA (gRNA and LNP are a plus).
- Familiarity with applicable ICH regulations and multi-compendial guidelines related to method validation.
- Experience in assay development, qualification, validation, and transfer to GMP environments.
- Proven track record of success collaborating effectively with cross-functional teams.
- Ability to balance multiple responsibilities, prioritize activities, and navigate ambiguity.
- Demonstrated learning agility, scientific problem solving, and strong written and verbal communication skills.
- Proactive, creative, and positive attitude.
- Unwavering commitment to safety protocols and procedures.
Preferred Qualifications:
- Experience working with various biophysical instrumentation such as GC, HIAC, and basic particle size characterization fluorescence-based assays.
- Strong understanding of SEC-MALS analytical methodology.
- Authorization to work in the United States indefinitely without restriction or sponsorship.
Additional Information
The position is full-time, first shift, Monday-Friday with overtime as needed. Candidates living within a commutable distance of Boston, MA are encouraged to apply.
Excellent full-time benefits include:
- Comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
- Compensation: $37.00-$41.00 per hour based on education and experience
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
