Quality Control Supervisor - Lab & GMP Lead

fairlife

Town of Webster (NY)

Vor Ort

USD 75.000 - 85.000

Vollzeit

Vor 11 Tagen
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Eine vollständige Bewerbung in einer Minute — maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Benefits dieser Stelle

Health coverage
Paid time off
401(k) matching

Zusammenfassung

fairlife is seeking a Quality Control Supervisor to lead daily QA activities, coordinate the laboratory and QC staff, and liaise between production and quality teams. The role requires ensuring compliance with GMP, HACCP, FDA and state regulations while driving continuous improvement in quality programs.

The position follows a rotating 12-hour schedule (6:00 AM–6:00 PM) with weekend work and occasional shifts, reporting to the QC Manager.

Qualifikationen

  • Bachelor's degree in a science preferred or management related discipline or at minimum of 5 years of experience that is directly related to the duties and responsibilities specified in a consumer package environment.
  • Ability to work in a fast paced, entrepreneurial environment.
  • PCQI trained individual (will provide if needed).

Aufgaben

  • Assists with and administers the quality systems for the facility which includes the daily management of the laboratory and Quality Control staff.
  • Aids and works towards continuously improving the administration and interpretation of quality control systems and policies, procedures, and documentation to subordinates and peers.
  • Assists with investigations and makes recommendations as appropriate regarding issues of product quality, advice, and guidance to management in these areas, as appropriate.

Kenntnisse

Supervisor experience
PCQI trained
Ability to work fast paced

Ausbildung

Bachelor's degree in science or related discipline
5+ years consumer packaged goods experience

Tools

Quality systems knowledge

Jobbeschreibung

fairlife is seeking a Quality Control Supervisor to lead daily QA activities, coordinate the laboratory and QC staff, and liaise between production and quality teams. The role requires ensuring compliance with GMP, HACCP, FDA and state regulations while driving continuous improvement in quality programs.

The position follows a rotating 12-hour schedule (6:00 AM–6:00 PM) with weekend work and occasional shifts, reporting to the QC Manager.

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