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Specialist Manufacturing

GPS Staffing Thousand Oaks, CA
  • Expired: 12 days ago. Applications are no longer accepted.

GPS Staffing is a nationwide preferred provider of staffing and recruitment services. GPS has over 25 years of dedicated staffing partnerships with organizations ranging from International Fortune 500 companies to Colorado startups. Our team is committed to Growth, People and Success!

Title: Specialist Manufacturing
Job ID: 6069
Industry: Biotech/Pharmaceutical
Location: Thousand Oaks, CA
Duration: 6-Month Contract with possible extension
Pay Rate: Depends on Experience (Hourly W2)

Job Details:
The Specialist is expected to own deviations, CAPA, CAPA-EV, supplier investigations (SICAR & EN), Change Control and have metrics oversight responsibilities. Experience with managing multiple records is important and TrackWise user knowledge is an advantage.

  • May act as the External Supply Lead driving consistency across all Specialists in the space.
  • Will be required to communicate with many functions within the organization, facilitate development of solutions to critical business issues, and effectively define objectives to enable effective metric generation and reporting.
  • May serve as the primary point of contact between Site Plant Quality and the corporate Supplier Quality Management team to ensure the quality of raw materials used at the sites.

Preferred Qualifications:

  • 6+ years related work experience (manufacturing, process development, or quality assurance) in in Biotech or pharmaceutical industry with progressively increasing responsibility and demonstrated experience in compliance, problem solving, advance root cause analysis, critical thinking, project management, and quality systems.
  • Thorough understanding of quality management systems and quality control processes related to Raw Materials utilization in clinical and commercial operations.
  • Thorough working knowledge of owning deviations, CAPAs, CAPA-EVs and change controls
  • Demonstrated ability to work autonomously, present data in an organized and logical manner, and communicate effectively
  • Demonstrated ability to navigate through ambiguity and provide a structured problem-solving approach.
  • Excellent interpersonal relationship skills.
  • Excellent oral and written communication skills.
  • Proficient with TrackWise; MSWord; MS Excel; MS PowerPoint
  • Ability to maintain remote working relationships with colleagues at other company sites.

Top Must Have Skills:

  • Thorough working knowledge of owning deviations, CAPAs, CAPA-EVs and change controls
  • 6+ years related work experience (manufacturing, process development, or quality assurance) in in Biotech or pharmaceutical industry with progressively increasing responsibility and demonstrated experience in compliance, problem solving, advance root cause analysis, critical thinking, project management, and quality systems.
  • Thorough understanding of quality management systems and quality control processes related to Raw Materials utilization in clinical and commercial operations.

Education Required:

  • Master's degree and 4 years of Quality and/or Manufacturing experience OR
  • Bachelor's degree and 6 years of Quality and/or Manufacturing experience OR
  • Associate's degree and 8 years of Quality and/or Manufacturing experience OR
  • High school diploma / GED and 10 years Quality and/or Manufacturing experience




Applicants:
We will not respond to everyone personally - qualified candidates will be contacted for a screening.
Please submit your resume in a word document.

GPS Staffing

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Thousand Oaks, CA
USA

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