- Performs routine sample analysis, and a variety of tasks to support product development, ensuring agreed timelines
- Assists method development
- Performs method validation under supervision
- Reports and resolved any unexpected issues under supervision
- Complies with all relevant cGMP, and/or GLP regulatory requirements while carrying out assigned studies
- B.S. in Chemistry, or related discipline with 3-5 years relevant experience in pharmaceutical, or related industry
- M.S. or PhD in Chemistry
- Hands-on experience with HPLC, UPLC, GC, LC/MS, IC, and Dissolution Testing
- Excellent oral and written communication skills
- Capable of setting priorities based on a fast-paced changing environment
- Good team player to work with Formulators and QA
- CRO experience is a plus
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Frontage Laboratories Exton, United StatesJob Description · Job DescriptionAssociate Scientist, Pharmaceutical Analysis-Small MoleculeExton, PA (Research) · ResponsibilitiesPerforms routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines · Assists method development Perfor ...
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Frontage Laboratories Exton, United StatesJob Description · Job DescriptionScientist/Senior Scientist - Pharmaceutical Analysis - Large MoleculeExton, PA (Research) · Roles and Responsibilities: · Develop and apply biochemistry, biophysics methods, immunoassays, and other state of the art analytical technologies to analy ...
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Scientist/Sr. Scientist Pharmaceutical Analysis-Small Molecule - Exton, United States - Frontage Laboratories
Description
Job Description
Job DescriptionScientist/Sr Scientist, Pharmaceutical Analysis-Small MoleculeExton, PA (Research)
Responsibilities:
Requirements:
Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.
