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Chemist; Quality Control Specialist
2 months ago
We are seeking a highly skilled and experienced Chemist to join our team at Contract Pharmacal. As a key member of our Quality Control department, you will be responsible for performing chemical analysis and ensuring the quality of our products.
Key Responsibilities- Perform routine laboratory chemical analysis on finished product, stability, raw material, and/or investigation samples, as assigned, using HPLC, UPLC, GC, UV-vis, FTIR, ICP, TOC and other wet chemistry techniques in accordance with the prescribed approved analytical test method.
- Maintain a clean and organized laboratory working environment, adhering to all laboratory SOPs, including but not limited to laboratory safety, chemical handling and storage, gowning, equipment use, cGMP, GDP, data integrity, DEA requirements, etc.
- Dispose of used/expired/excess chemicals, solutions, solvents, etc. in dedicated waste receptacles, ensuring compliance with all regulatory requirements.
- Report well-written, accurate and timely results, reviewing data, calculations, notebooks, and reports to ensure accuracy and completeness.
- Assist in laboratory investigations, as assigned, and participate in Cleaning, Method and Process validation testing and protocol/report review, as assigned.
- Maintain and troubleshoot laboratory equipment, suggesting improvements to existing testing methods when possible.
- Mentor and give guidance to entry-level personnel on techniques performed in the lab, assisting with laboratory related questions as needed.
- Assist with routine Metrology functions, including instrument cleaning/ preventive maintenance/ calibration/ verification activities, and monitor and assist with maintaining proper inventory levels of all laboratory supplies.
- Assist with sample receiving, chemical inventory, document filing, housekeeping, etc., and other responsibilities as assigned by Management.
- Bachelor's degree in a science related field.
- Between 1 and 9 years of work experience in a laboratory setting.
- Knowledge of laboratory chemistry and cGMPs.
- Proficient in Microsoft Word, Excel, graphs/charts and databases.
- Proficient in HPLC/UPLC, ICP, Dissolution, IR, UV/VIS, and wet chemistry testing.
- Proficient with analytical laboratory software.
- Able to multitask and meet tight deadlines.
- Excellent organizational skills with attention to detail.
- Able to effectively present results.
- Able to perform testing on many methods and troubleshoot minor method issues. May require some guidance/supervision as needed.
- Able to troubleshoot basic instrument issues independently and complex instrument issues under supervision.
- Required to sit and stand for long periods of time.
- Frequently reaching with arms/hands up to 2 feet.
- Good hand eye coordination.
- Occasionally required to walk and kneel.
- Must be able to lift and/or move up to 50 pounds.
- Must be able to use close vision, distance vision, peripheral vision, color vision and the ability to adjust focus.
- Required to reach with arms and use hands and fingers to handle or feel objects, tools and computer controls.
- Required to stoop, kneel, crouch, stand, bend, sit, talk, hear, climb stairs.
- Work environment in laboratory and production operations facilities include close proximity to heavy machinery and pharmaceutical powders.
- Potential to move between production operations sites/areas to complete job functions.
- Employee work hours/schedule and/or shift are subject to change based on business needs and Management discretion.
- Required to be present in the laboratory to perform daily testing and collaborate with department director, manager, and peers.
- Responsible for compliance with all rules and regulations pertaining to safety policies with the proper attitude toward safety and health, helping to ensure that all department operations are performed with the utmost regard for the safety and health for all personnel.
- None
- Gowning as required by GMPs and/or SOPs.