Quality Control Chemist III

2 days ago

north billerica, United States Randstad Life Sciences US Full time

4 Month Contract

North Billerica, MA

PR: $30-40/hour

Job Summary

Perform testing/review on incoming materials, in-process and finished products, and stability studies in QC Laboratory.


Job Responsibilities

  • Perform routine, non-routine and some advanced QC testing in accordance with SOPs and cGMP guidelines. Perform a wide variety of methods and utilize equipment ranging from basic to advanced. Limited supervision required.
  • Perform verification of data to ensure accuracy. Perform approval upon discretion of supervisor.
  • Assist with audit readiness of laboratory area and calibration and maintenance of laboratory equipment.
  • Utilize a range of electronic systems such as document/equipment management software, LIMS, Empower, and ERP.
  • Author and review SOP changes; participate in change controls, CAPAs and other quality systems.
  • Resolve routine and some advanced problems by utilizing appropriate resources. Provide problem solving skills to support investigations.
  • Participate in protocols for procedural and instrumentation validations.
  • Work on special projects as needed. Contribute towards continuous improvement.
  • Train on and maintain considerable knowledge of current regulatory requirements and relevant internal procedures.
  • Work independently and as a team player with quality and attention to detail. Good communication skills both oral and written. Effectively and efficiently participate in assigned tasks in a quality manner.
  • Actively promote safety rules and awareness. Report and take initiative to correct safety & environmental hazards. Work with potentially hazardous chemical, radiological and/or biological materials on a daily basis. Demonstrate good safety practices at all times including the appropriate use of protective equipment.
  • Promote and actively demonstrate the values of Accountability, Quality, Efficiency, Customer Service, Collaboration, and Safety, as well as appropriate workplace behaviors and professionalism, including respect, flexibility, and a positive attitude toward work and others.


Education & Qualifications

  • Typically requires 3-5 years with a BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and previous relevant experience in the pharmaceutical industry, related GMP environment, or equivalent.
  • Previous analytical chemistry including HPLC, GC and AA experience preferred, also previous radiological and/or physical testing experience beneficial.
  • Routinely scheduled work may be required on evenings, weekends, and/or holidays, including during adverse weather conditions. Some non-routine travel may be required.
  • Work with (or in proximity to) potentially hazardous chemical, radiological, and or biological materials and must be able to lift/move materials, e.g. portable equipment, lead, gas cylinders, bottles of chemicals/waste containers

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