Precision Formulation Tech II — GMP Reagent Production

bioMerieux Inc.

Durham (NC)

Vor Ort

USD 32.000 - 42.000

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Medical, dental, and vision plans
Retirement plan with employer match
Wellness programs
Commuter benefits

Zusammenfassung

bioMerieux Inc. seeks a Formulation Technician II to process and formulate bulk liquids, polymers, and biologicals for reagent manufacturing. The role emphasizes GMP compliance, Right First Time, and precise documentation, with potential to handle multiple formulations per shift.

Responsibilities include setup, operation, inspection, cleaning of equipment, obtaining in-process samples, and collaborating with QA/QC. Requires 2+ years in regulated production and a high school diploma.

Qualifikationen

  • Detail-oriented, accurate execution in GMP environment.
  • Ability to document processes and results with clarity.
  • Experience in regulated production/operations settings.
  • Familiarity with SOPs, GMP and regulatory standards.
  • Lean/CI training is a plus for process improvements.

Aufgaben

  • Operate formulation equipment per approved manufacturing directions and SOPs.
  • Complete batch documentation and in-process sampling with accuracy.
  • Maintain clean, cGMP-compliant work areas and participate in safety audits.
  • Collaborate with QA/QC and senior staff to meet production goals.
  • Support validations, tech transfers and process improvements.

Kenntnisse

Detail orientation
Cross-functional collaboration
Verbal communication
Documentation proficiency
SOP/regulatory knowledge
Quality ownership

Ausbildung

High School Diploma, GED or equivalent
BioWorks LEAN or Continuous Improvement Certificate

Jobbeschreibung

bioMerieux Inc. seeks a Formulation Technician II to process and formulate bulk liquids, polymers, and biologicals for reagent manufacturing. The role emphasizes GMP compliance, Right First Time, and precise documentation, with potential to handle multiple formulations per shift.

Responsibilities include setup, operation, inspection, cleaning of equipment, obtaining in-process samples, and collaborating with QA/QC. Requires 2+ years in regulated production and a high school diploma.

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