Co-Manufacturing Quality Assurance Specialist (Equity)

David Protein

New York (NY)

On-site

USD 95,000 - 110,000

Full time

14 days+
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Benefits offered by this job

Company equity options
100% covered Health, Vision, Dental
401(k) with 4% match
Covered gym expenses
Substantial PTO

Job summary

Medici Brands in New York City is seeking a Third-Party Manufacturing (3PM) Quality Associate to support day-to-day quality management across David’s contract manufacturers, ensuring compliance with food safety, product specifications, COAs, and documentation.

You will collaborate with Quality, Manufacturing, R&D, and suppliers to drive lot release, CAPAs, audits, and continuous improvement across the external manufacturing network.

Qualifications

  • Background in Food Science or regulatory-related field.
  • Experience in food, beverage, or CPG quality.
  • Knowledge of FDA, FSMA, GFSI, HACCP, Prop 65.
  • Strong documentation and organizational skills.
  • Cross-functional teamwork in fast-paced environments.

Responsibilities

  • Support qualification and onboarding of new contract manufacturers.
  • Coordinate collection/review of co-man documentation and quality records.
  • Maintain co-man onboarding materials and quality agreements.
  • Participate in audits, site visits, and quality meetings.
  • Maintain audit schedules and track follow-ups.
  • Track CAPAs and non-conformances and escalate issues.
  • Maintain dashboards and scorecards for quality and operations.
  • Translate development requirements into manufacturing specs and quality docs.

Skills

Cross-functional collaboration
Documentation discipline
Regulatory knowledge
Attention to detail
Travel willingness

Education

Bachelor's degree in Food Science or related field

Tools

TraceGains

Job description

Medici Brands in New York City is seeking a Third-Party Manufacturing (3PM) Quality Associate to support day-to-day quality management across David’s contract manufacturers, ensuring compliance with food safety, product specifications, COAs, and documentation.

You will collaborate with Quality, Manufacturing, R&D, and suppliers to drive lot release, CAPAs, audits, and continuous improvement across the external manufacturing network.

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