QC Scientist I
3 months ago
In this role you will use numerous analytical tools used for large molecule analysis, such as HPLC, UPLC and other minor equipments. This work will be supporting GMP manufacturing for early and late state clinical and commercial efforts (In-Process) along with Stability testing and other endeavors requested by the client. This role will require experience in working in a cGMP environment. The candidate should be familiar with using Empower software.
What will you do?
Perform HPLC/UPLC testing on In-Process, DS release, DP release, DS stability, DP Stability, and various other non-routine samples, ensuring timely delivery for projects Conduct GMP testing in an analytical laboratory environment using HPLC and UPLC test methods (,Reverse Phase, SEC, Titer concentration, CEX, etc) Compiles data for documentation of test procedures, prepares reports. Collaborate with team members and other departments such as quality assurance and data reviewers. Contributes to the development of new concepts, techniques, and standards. Recognize and report invalid/ lab incident/ out-of-specification/ out-of-trend results to laboratory management; recommend solutions. Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, and Safety guidelines. Participate in laboratory activities, performing safety inspections and ordering supplies.How will you get here?
Required: Bachelor’s degree in chemical pharmaceutical, biology, chemistry, biotechnology or related field or equivalent work experience and knowledge In-depth knowledge of the most common analytical techniques and required instrumentation (HPLC, UPLC, etc..) Knowledge of MS Office and laboratory computer programsPersonality traits:
Flexibility Good organization and planning skills Attention to details Positive and collaborative demeanour-
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