ELISA Manufacturing Associate I – Entry‑Level

Werfen

Oceanside (CA)

Vor Ort

USD 32.000 - 40.000

Vollzeit

Vor 13 Tagen

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Benefits dieser Stelle

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Paid Vacation
Paid Sick Leave
Commission Plan
Performance-based Bonus

Zusammenfassung

Werfen, a global leader in diagnostics, seeks a Manufacturing Associate I for the ELISA Plates team in California. You will operate manufacturing equipment, support ELISA plate production, and ensure quality control throughout the process while maintaining proper documentation and adherence to procedures.

Work in a regulated manufacturing environment, collaborate with cross-functional teams, and develop skills in troubleshooting, equipment validation, and continuous improvement for long-term

Qualifikationen

  • Basic understanding of basic laboratory practices and procedures.
  • Basic understanding of Good Manufacturing Practices.
  • Strong attention to detail and commitment to quality.

Aufgaben

  • Follows SOPs and work instructions for routine manufacturing and/or testing.
  • Supports bulking and evaluation of in-process components and reagents.
  • Packages, fills, and operates equipment to complete in-process components.
  • Maintains Device History Records and related manufacturing documentation.
  • Operates and cleans equipment and instrumentation for routine manufacturing/testing.
  • Assists with evaluations of raw materials.
  • Follows safety and environmental procedures.
  • Keeps lab and work area clean and orderly.
  • Complies with Werfen SOPs, ISO, FDA and other Quality System regulations.

Kenntnisse

Attention to detail
Teamwork
Problem solving
Time management

Ausbildung

Bachelor's degree in Biological or related sciences

Jobbeschreibung

Werfen, a global leader in diagnostics, seeks a Manufacturing Associate I for the ELISA Plates team in California. You will operate manufacturing equipment, support ELISA plate production, and ensure quality control throughout the process while maintaining proper documentation and adherence to procedures.

Work in a regulated manufacturing environment, collaborate with cross-functional teams, and develop skills in troubleshooting, equipment validation, and continuous improvement for long-term

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