Associate Scientist, Quality Control

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Associate Scientist, Quality Control

• Perform physical and chemical testing of raw material, packaging material, in-process, release, and stability samples.
• Record experimental data, analyze results, and maintain accurate and up-to-date notebooks.
• Assist in maintaining the laboratory in compliance with SOPs, CGMPs, FDA, OSHA and other guidelines.
• Assist in filing laboratory documents.
• Use and maintain instruments, such as HPLC, GC, Dissolution, UV-VIS, IR, Titrator, etc.
• Troubleshoot and perform minor maintenance and repair of lab instrumentation.
• Support investigation and troubleshooting of analytical issues.
• Carry out duties in compliance with all state and federal regulations and guidelines including FDA, DEA, EPA and OSHA.
• Support ANDA/NDA projects from development to approval with guidance.
• Support method development and method validation work.
• Perform calibration and maintenance of various analytical equipment.
• Assist in writing technical documents (for example specifications, test methods, protocols and reports).
• Periodically review SOPs for compliance with CGMP and revise SOPs, if necessary.
• Execute EQ protocols and set up qualification program for new instruments with some guidance.
• Perform calibration and maintenance of various analytical equipment.
• Assist in preparing documents for ANDA/NDA filing.
• Provide formal/informal mentoring to technicians.

• Maintain laboratory in clean and organized condition.
• Order, receive and maintain a record of chemicals and lab supplies.
• Perform regular inspection of chemical storage areas to ensure the proper storage of chemicals and to remove expired chemicals from storage.
• Packaging all samples to be sent out.
• Dispose laboratory organic waste and solid waste timely manner.
• Assist in filing of laboratory documents.

• Strong verbal and written communication skills.
• Demonstrated proficiency with General Chemistry and various analytical instruments (HPLC, Dissolution, GC, UV-VIS, IR, etc.)
• Ability to multi-task and prioritize.
• Prior experience with CGMP.
• Must be capable of performing routine / new procedures with minimal direct supervision.
• Must be able to understand technical terminology, names of drugs and ingredients used.
• Must have good understanding of basic statistics and be able to analyze/plot data in an understandable fashion.

• BS in Chemistry or Pharmaceutical sciences with 1-3 years of relevant pharma laboratory experience.

• Light work (exerting up to 20 pounds of forces occasionally, and/or up to 10 pounds of force frequently) to medium work (exerting up to 50 pounds of forces occasionally, and/or up to 30 pounds of force frequently).
• Stooping-bending body downward and forward by bending spine at the waist.
• Reaching-extending hand(s) and arm(s) in any direction.
• Standing-particularly for sustained periods of time.
• Walking-moving about on foot to accomplish tasks, particularly for long distances or moving from one work site to another.
• Subject to Noise-sufficient noise to cause worker to shout in order to be heard above ambient noise level.
• Subject to proximity to moving mechanical parts, or exposure to chemicals.