Manufacturing Process Technician

4 weeks ago


Thousand Oaks, California, United States Quality Consulting Group Full time
Job Description

Quality Consulting Group is seeking a highly motivated and detail-oriented Manufacturing Process Technician to join our team in Puerto Rico & USA. In this role, you will contribute to a world-class manufacturing industry, working closely with a highly enthusiastic team.

Key Responsibilities:

  • Provide facility/equipment cleaning and sanitation in support of FDA regulated manufacturing areas, ensuring minimal impact on production while complying with Standard Operating Procedure's (SOP's) and Current Good Manufacturing Practices (cGMP's).
  • Follow Good Manufacturing Practices (GMPs) and applicable regulations from the Code of Federal Regulations (CFRs).
  • Report any discrepancies to the Team Leader or Production Supervisor to ensure quality standards and safety.
  • Ensure quality & compliance through a Right First-Time mentality.
  • Receive and prepare components for use in manufacturing.
  • Feed components into equipment and perform sanitation activities.
  • Document appropriate paperwork, understand Overall Equipment Effectiveness (OEE)/performance metrics, and participate in daily performance meetings.
  • Use pallet jacks and manual wrapping of pallets.
  • Use computer systems to support material inventory and electronic batch record.
  • Partner with cross-functional teams to drive improvement opportunities.
  • Ensure components and products are available for continuous operation.

Qualifications:

  • Associate degree and 2 years of experience OR 2 years in a technical school setting with hands-on experience OR High school diploma / GED and 4 years of experience.
  • Previous experience working as a technician, in med device or pharma.
  • Aseptic background Component preparation.
  • Capable of working on their feet for long periods of time / physical activity.
  • Experience with cleaning manufacturing areas/ previous work in a manufacturing area.
  • Must read and write in English.
  • Experience in a cGMP Grade 8 or lower environment is preferable.
  • Hours: 7am -4 pm Day shift but possible to move to a split shift of 3pm-12am in the future if extended. Flexibility with schedule, open to overtime.

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.



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