Eurofins PSS Insourcing Solutions
Job Description
Responsible for utilizing analytical methodologies, systems, and processes to support GMP release and stability testing of clinical supplies for drug substance and drug product throughout all phases of development. This may include excipient, packaging, and post packaging support.
Analytical testing includes compendial testing (e.g., excipients/packaging release testing), disintegration, dissolution, HPLC/UPLC, SFC, generic testing (e.g., solvents, water, ash, titrations, heavy metals, ICP/MS, UV), and compound specific methods.
Set up and analyze drug substance and drug product stability samples.
Method development and validation of analytical methods for drug substance and drug product.
Qualifications
Strong computer, scientific, and organizational skills.
Experience with eLN, LIMS, and data trending is a plus.
Excellent communication (oral and written) and attention to detail.
Ability to work independently and as part of a team, self‑motivated, adaptable, and a positive attitude.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Minimum Qualifications
Bachelor’s degree in chemistry or other science related degree concentration, or equivalent directly related experience.
Laboratory experience and some experience in GMP analytical chemistry, preferred.
Additional Information
Position is Monday-Friday 8:00am – 5:00pm, overtime as needed.
Candidates currently living within a commutable distance of Groton, CT are encouraged to apply.
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.
Authorization to work in the United States indefinitely without restriction or sponsorship.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
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Responsible for utilizing analytical methodologies, systems, and processes to support GMP release and stability testing of clinical supplies for drug substance and drug product throughout all phases of development. This may include excipient, packaging, and post packaging support.
Analytical testing includes compendial testing (e.g., excipients/packaging release testing), disintegration, dissolution, HPLC/UPLC, SFC, generic testing (e.g., solvents, water, ash, titrations, heavy metals, ICP/MS, UV), and compound specific methods.
Set up and analyze drug substance and drug product stability samples.
Method development and validation of analytical methods for drug substance and drug product.
Qualifications
Strong computer, scientific, and organizational skills.
Experience with eLN, LIMS, and data trending is a plus.
Excellent communication (oral and written) and attention to detail.
Ability to work independently and as part of a team, self‑motivated, adaptable, and a positive attitude.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Minimum Qualifications
Bachelor’s degree in chemistry or other science related degree concentration, or equivalent directly related experience.
Laboratory experience and some experience in GMP analytical chemistry, preferred.
Additional Information
Position is Monday-Friday 8:00am – 5:00pm, overtime as needed.
Candidates currently living within a commutable distance of Groton, CT are encouraged to apply.
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.
Authorization to work in the United States indefinitely without restriction or sponsorship.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
#J-18808-Ljbffr