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Senior Quality Assurance Specialist

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Senior Quality Assurance Specialist

  • Sector:

    Pharmaceutical

  • Job type:

    Full Time Direct Hire

  • Contact:

    Jasleen Kaur

  • Contact email:

    Jasleen Kaur

  • Contact phone:

    Jasleen Kaur

  • Job ref:

    5268

  • Published:

    about 2 months ago

  • Expiry date:

    02 Dec 00:00

Senior Quality Assurance Specialist

Edison, NJ

Job ID:5268

Are you looking to make a career change to a stable company? This exciting opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance and paid PTO.Does this position match your future career goals?Then this opportunity could be the right fit for you.

 

Must have experience in Pharmaceutical Manufacturing

  • Growth Opportunities
  • Great Pay
  • A Positive Work Environment
  • Business hours

 

Job Requirements:

  • Bachelor's degree in Chemistry, Pharmaceutical or similar.
  • Be able to perform all IPQA (In-Process Quality Assurance) functions.
  • Working knowledge of root cause analysis tools.
  • Initiate, review, monitor and track all Deviations, CAPA’S throughout the company.
  • Previous work experience with FDA audits.
  • Review current SOP’s, policies and systems.
  • Knowledge of the pharmaceutical manufacturing.
  • Demonstrated leadership skills in a manufacturing environment
  • Demonstrate safe behavior and support department/plant Safety goals in a continuous improvement process.
  • Supports documentation
  • Performance of Risk Assessments
  • Ensure compliance with Good Manufacturing Practices (GMP) FDA inspection and all related regulatory guidelines.
  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals
  • Monitor the manufacturing equipment and rooms and packaging lines/ equipment.
  • Be able to perform incoming and outgoing inspections of finished product batches.
  • Follow written , approved procedures to maintain cGMP standards.
  • Inspect and evaluate procedures and processes for production.
  • Analyze data, create reports and communicate feedback.
  • Train teams to reduce quality problems and increase understanding of quality goals.
  • Document current state, risks, and process improvement goals.
  • Ensures compliance with cGMP, Company SOPs and FDA requirements during all phase of operations.
  • Performs process checks and verification's to ensure the quality is maintained.

 

Ask for Jasleen

jasleen@ajuliaexecutivesearch.com

Ajulia Executive Search is a search firm specializing in Manufacturing, Finance, IT, Legal and Pharmaceutical positions. This is a confidential search for one of our preferred clients. It is a direct hire position that includes competitive compensation and full comprehensive benefit package.

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