Temporary- Scientist II Quality Control, 3-6 Months
Amneal Pharmaceuticals
The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture.
Essential Functions:
Additional Responsibilities:
Assists, as and when needed, senior scientists working in the laboratory. Ensures that expired chemicals and reference standards are removed from laboratory area, performs calibration of dissolution apparatus, FT-IR, UV-Vis spectrophotometer, HPLC, GC as assigned by the supervisor. Standardizes API for use as in-house reference standard as assigned. Interacts with newly hired laboratory technicians or Assistant Scientists for providing hands-on training on simple analytical techniques and laboratory instruments. Qualifications for Internal CandidatesEducation:
Bachelors Degree (BA/BS) Chemistry or related science discipline - Required Master Degree (MBA) Chemistry or related science discipline - PreferredExperience:
3 years or more in Bachelors Degree (BA/BS) -Testing of chemicals/pharmaceutical products, 3 years or more 1 year or more in Master Degree (MA/MS) -Testing of chemicals/pharmaceutical products, 1 years or moreSkills:
Must be precise and consistent in day-to-day analysis, using sophisticated analytical instruments. - Advanced Must be familiar with out of specification and out of alert limit investigations. - Intermediate Must be able to execute compendial procedures involving complexity. - Intermediate Must be familiar with cGMP and OSHA regulations. - Intermediate Must be able to effectively communicate results, problems or issues, verbally as well as in writing. - Intermediate Must be computer literate and savvy with MS office applications, software programs related to LIMS. - Intermediate Must be able to work in a team environment and be flexible to easily adapt to changes in assignments. - Intermediate Must follow safe practices as identified in appropriate MSDS during working with chemicals, and must follow applicable state and federal regulations. - Intermediate Must be capable of maintaining clear and concise laboratory records and communicating clearly both within and between departments. - Intermediate Must be thoroughly familiar with cGMP applicable to laboratories in pharmaceutical settings and with method verification/validation concepts. Must be able to review laboratory records to ascertain compliance with applicable specifications, methods, and SOPs. - Intermediate Must be able to assume a role of a leader in team environment as and when required. - Beginner
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