Associate Scientist: Drug Product Development job in New Haven, USA

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Job type: Contract

Discipline: Biochemistry

Location: United States

This vacancy has now expired. Please see similar roles below...

Associate Scientist: Drug Product Development - Contract - New Haven, CT

Proclinical is seeking an Associate Scientist for Drug Product Development. In this role, you will design and execute development studies for clinical drug candidates and commercial products, focusing on characterizing protein drug stability using industry-standard methodologies. You will work both independently and as part of a team, prioritizing multiple tasks and projects.

Primary Responsibilities:

The successful candidate will design and execute development studies for clinical drug candidates and commercial products, focusing on characterizing protein drug stability using industry-standard methodologies. They will work both independently and as part of a team, prioritizing multiple tasks and projects.

Skills & Requirements:

Degree in Biochemistry, Pharmaceutical Science, Chemical Engineering, or a relevant field.
Understanding of protein stability, thermodynamics, and protein degradation mechanisms.
Experience with H/UPLC, imaged capillary electrophoresis (iCE/Maurice), Ion Exchange Chromatography (IEX), Micro-flow imaging (MFI), light obscuration (LO), DLS, NanoTemper, and DSC.
Proficiency in MS Office programs, including Word, Excel, Outlook, and PowerPoint.
Experience with sub-visible particulates characterization and testing is preferred.
Familiarity with biophysical and analytical testing.
Knowledge of regulatory guidelines.
Experience with electronic record-keeping software like ELN, EndNote, and e-logbooks is a plus.
Ability to take initiative in problem-solving and finding scientific solutions.
Strong communication and collaboration skills.

The Associate Scientist: Drug Product Development's responsibilities will be:

Design and execute development studies for clinical drug candidates and commercial products.
Characterize protein drug conformational and colloidal stability using methods such as circular dichroism, differential scanning fluorimetry, analytical ultracentrifugation, and size-exclusion chromatography.
Conduct physicochemical characterization, particulate testing, and stability studies.
Assist in preparing internal technical reports on executed studies.
Participate in cross-functional development teams.

Compensation:

USD 18.00 - 22.75 per hour

If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at s.briggs@proclinical.com

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

Salary

Highly Competitive

Location:

Cambridge, USA

Proclinical is working alongside a pharmaceutical company to recruit for a Sample Management and Stability Coordinator. This is a temporary contract position based in Cambridge, Massachusetts.