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Scientist III-Analytical Sciences

Parexel International Corporation

Hackensack, New Jersey, United States

This role requires a College or University (graduate school) degree in Chemistry, Pharmaceutical Sciences, other Life Sciences, or equivalent. Minimum 5 years of experience with a Bachelor's degree preferred. Minimum 1-2 years of relevant industry experience for applicants with a Master's degree preferred. Experience with chromatographic analysis using various UPLC and HPLC techniques. Experience with Empower chromatographic data program and with analysis of oral solid dosage forms preferred. Experience with dissolution, water activity, Karl Fischer titration preferred. A proven record of technical problem-solving experience with standard operating procedures and cGMP analytical testing. Excellent communication (oral and written) and attention to detail. Excellent organization to multi-task and manage multiple projects. Ability to work as part of a team, self-motivation, adaptability, and a positive attitude Conducts release and stability testing of drug products following SOPs and cGMPs. Plans and executes validation of analytical methods; may develop and/or adapt methods Solves more complex problems with some guidance from senior scientists Troubleshoots instrumentation May investigate new technologies Documents results in ELN and RLIMS and performs second chemist review May author analytical reports and SOPs. Receives mentorship from scientific supervisor Carries out all assignments to the standards of efficiency, innovation, accuracy, and safety in accordance with Company and regulatory requirements. Provides analytical support to development projects, research activities within Analytical Sciences. Prior experience working with inhalation products is a plus. QualificationsThis role requires a College or University (graduate school) degree in Chemistry, Pharmaceutical Sciences, other Life Sciences, or equivalent. Minimum 5 years of experience with a Bachelor's degree preferred. Minimum 1-2 years of relevant industry experience for applicants with a Master's degree preferred. Experience with chromatographic analysis using various UPLC and HPLC techniques. Experience with Empower chromatographic data program and with analysis of oral solid dosage forms preferred. Experience with dissolution, water activity, Karl Fischer titration preferred. A proven record of technical problem-solving experience with standard operating procedures and cGMP analytical testing. Excellent communication (oral and written) and attention to detail. Excellent organization to multi-task and manage multiple projects. Ability to work as part of a team, self-motivation, adaptability, and a positive attitude Conducts release and stability testing of drug products following SOPs and cGMPs. Plans and executes validation of analytical methods; may develop and/or adapt methods Solves more complex problems with some guidance from senior scientists Troubleshoots instrumentation May investigate new technologies Documents results in ELN and RLIMS and performs second chemist review May author analytical reports and SOPs. Receives mentorship from scientific supervisor Carries out all assignments to the standards of efficiency, innovation, accuracy, and safety in accordance with Company and regulatory requirements. Provides analytical support to development projects, research activities within Analytical Sciences. Prior experience working with inhalation products is a plus. EEO DisclaimerParexel is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Job posted: 2021-05-15

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