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QC Methods Development Scientist (cGMP – Pharmaceutical) JD818692

JD818692

DPS Engineering is looking for a capable Methods Validation professional to support a Biopharma client in the Boston, MA area. This individual will be responsible for the development of new equipment, methodologies, concepts, techniques, and standards for Quality Control.

Category:
Science
Location:
Massachusetts
Years of Experience Req.:
5+
Date Posted:
15/06/2020
Days Remaining:
30
Employment Type:
Full-time
Education Level Req.:
Bachelors

QC Methods Development Scientist (cGMP – Pharmaceutical)      JD818692

Boston, MA area

 

Summary:

 

DPS Engineering is looking for a capable Methods Validation professional to support a Biopharma client in the Boston, MA area. This individual will be responsible for the development of new equipment, methodologies, concepts, techniques, and standards for Quality Control.

 

Job Responsibilities:

  • Contributes to the development of new concepts, techniques, and standards. Considered a consultant (expert) within the group. Has complete understanding and application of principles, concepts, practices, and standards.
  • Responsible for conducting analyses of raw materials, manufacturing samples, in-process and finished products and formulations according to SOPs.
  • Compiles data for documentation of test procedures and prepares reports.
  • Review IQ/OQ/PQ protocols and final reports for instrument system upgrades. Generates PQ protocols.

 

Qualifications:

  • Bachelor’s Degree in Life Sciences.
  • At least 5+ years of related experience or equivalent combination of education and experience.
  • Extensive knowledge of QC testing principles and procedures.
  • Extensive exposure to cGMP environment.
  • Knowledge of testing and associated equipment protocols and requirements and applicable instrumentation and procedures.
  • Strong interpersonal and communications skills; written and oral.
  • Solid understanding of applicable regulatory requirements.
  • Significant laboratory documentation review and revision experience.
  • Ability to function well in a fast-paced environment.
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