Senior Quality Assurance Consultant - Irvine, CA (REF7378G)

Senior Quality Assurance Consultant - Irvine, CA (REF7378G)

27 Jan 2024
California, Irvine, 92602 Irvine USA

Senior Quality Assurance Consultant - Irvine, CA (REF7378G)

Vacancy expired!

Job Description

Client is looking for a Senior Quality Assurance Consultant with a Sterilization/Microbiology background to perform the following tasks:

  • Investigations to uncover areas of non-conformance.
  • CAPA and SOP generation and review.
  • Provide support to clients on quality issues such as OOS results, deviations and non-conformances.
  • Provides Quality oversight of operations and data review for accuracy, completeness, and conformance to current Good Manufacturing Practices (cGMP) and company quality standards.
  • Provide training, executing audits, document creation, communication, and oversight to meet the established quality goals of the client and applicable regulations.
  • Provide assistance in performing internal and external GMP compliance audits and annual quality review.

Qualifications

  • Qualified candidates will possess a Bachelor’s degree in scientific or engineering discipline along with 5 plus years related industry experience.
  • Proficient in Microsoft Word, Excel, Power Point and Project.
  • General knowledge of quality system elements and cGMP regulations.
  • Experience providing support to clients with quality issues such as OOS results, deviations and non-conformances arise. Also, provide advisement for the implementation of proper CAPA to resolve deviations and non-conformances.
  • Ability to write and revise Standard Operating Procedures.
  • Effective written and oral communication skills; ability to write, type, express or exchange ideas; ability to convey information/instructions accurately.
  • Carry out duties and responsibilities with limited supervision.
  • Flexibility to work occasional weekends and evenings.
  • Ability to walk, stand and move about for long periods of time; work with equipment in the field including basic hand tools, lift and manipulate reasonable weights (approximately 35 lbs.), ability to sit and type for long periods of time.
  • Ability to plan and manage own work
  • Must be willing to travel regionally and/or nationally throughout the US.

Additional Information

All candidates must be legally eligible to work in the United States.

We are an equal opportunity employer. M/F/D/V

ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.

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Job Details

  • ID
    JC8668907
  • State
  • City
  • Job type
    Contract
  • Salary
    N/A
  • Hiring Company
    ProPharma Group
  • Date
    2021-01-20
  • Deadline
    2021-03-21
  • Category

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