Quality Control Specialist

3 weeks ago


Chelsea, Massachusetts, United States Catalent Inc Full time

Quality Control Analyst Role Summary:

Catalent Inc is seeking a Quality Control Analyst to support product development, release, and stability in a cGMP regulated environment. The ideal candidate will have a Bachelor's Degree in Physical or Chemical Sciences and 1+ years of experience in a similar role.

Key Responsibilities:

  • Conduct routine and non-routine chemical and physical analyses of raw materials, in-process materials, and drug products according to standard operating procedures.
  • Compile data for documentation of test procedures, including stability program testing and formulation studies.
  • Participate in the preparation of investigations, summaries, and reports, and review data obtained for compliance to specifications.
  • Identify and alert a supervisor of issues on instruments and/or test executions, and make initial recommendations for possible solutions and/or corrective actions.

Requirements:

  • Bachelor's Degree in Physical or Chemical Sciences.
  • 1+ years of experience in a cGMP regulated environment.
  • Experience in MDI/DPI analytical test methods, executing QC test methods, and troubleshooting instrumentation.
  • Excellent oral and written communication skills.

Why Catalent:

  • Defined career path and annual performance review and feedback process.
  • Diverse, inclusive culture.
  • Positive working environment focusing on continually improving processes to remain innovative.
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.

About Catalent:

Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide.

Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us.

Join us in making a difference.



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