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Quality Control Documentation Associate

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Quality Control Documentation Associate

  • Sector:

    Pharmaceutical

  • Job type:

    Contract to Hire

  • Contact:

    Karen Manteneri

  • Contact email:

    Karen Manteneri

  • Contact phone:

    Karen Manteneri

  • Job ref:

    4779

  • Published:

    23 days ago

  • Expiry date:

    2019-11-28

QC Documentation Associate

Princeton, NJ

 

Join our client’s team as a Documentation Specialist!  This position is full time, contract to permanent, competitive pay with overtime.  This job offers benefits including paid time off (PTO) and medical after 90 days.

Responsibilities:

  • To maintain the PD/TS/R&D documentation records.
  • To guide documentation associates (if any) in the preparation of PD/TS/R&D documentation.
  • To maintain the PD/TS SOP’s.
  • Preparation of Exhibit Batch Manufacturing and Packaging Batch Records and Commercial Batch Manufacturing and Packaging batch Records.
  • Preparation of Exhibit batch qualification protocols, Product evaluation protocols and Process validation protocols.
  • Preparation of Development Reports and Process validation reports.
  • Preparation of change controls as per the requirement.
  • Support the PD/TS/R&D Scientist/Research Associates for documentation.
  • Perform other related duties as required and/or assigned

Qualifications:

  • Pharmaceutical experience is required
  • Minimum Bachelor’s Degree of Science

Benefits:

  • This job offers benefits including paid time off (PTO) and medical after 90 days.

Ask for: Karen Manteneri or Nilam Patel

nilam@ajuliaexecutivesearch.com

 

Ajulia Executive Search is a New Jersey based Executive Search Firm specializing in retained searches in multiple sectors, including Manufacturing, Finance, IT, Legal, and Pharmaceutical. We have a nationwide client base and offer services in temporary and direct hire placements.

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