GMP Manufacturing Lead: Scheduling, Quality & Compliance

PROMED MOLDED PRODUCTS INC

Plymouth (MN)

On-site

USD 85,000 - 125,000

Full time

14 days+
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Benefits offered by this job

401k with company match
Profit Sharing Program
Medical Insurance
Health Savings Account / Flexible...
Vision Insurance
Life Insurance
Paid Family Medical Leave
Long‑Term Disability Insurance
Hospital Indemnity
Critical Illness
Accident Insurance
Identity Theft Protection
Pet Insurance

Job summary

Promed Molded Products Inc. is seeking a GMP Manufacturing Lead to ensure smooth, compliant production scheduling and disciplined documentation on the manufacturing floor in Plymouth, Minnesota.

The role coordinates the people, materials, and systems to execute batches right the first time, working cross-functionally with Quality, Materials, and Manufacturing to maintain compliance. The candidate will manage GMP scheduling, ERP/MRP material setup, operator training, and production record review,

Qualifications

  • High school diploma or equivalent; technical degree preferred.
  • 3+ years in pharma/biotech GMP manufacturing with scheduling or lead operator experience.
  • Experience with batch records, GDP, and ERP/MRP systems; CAPA/deviation exposure.

Responsibilities

  • GMP Production Scheduling across client programs and ensure on-time batches.
  • Material setup in ERP and ensure BOM accuracy.
  • Operator training and qualification on SOPs and batch records.
  • Review batch and packaging records for GDP compliance.
  • Initiate deviation reports and support CAPA investigations.
  • Coordinate with Quality, Planning, and Materials to resolve issues.

Skills

GMP manufacturing
Production scheduling
Batch record review
GDP
CAPA investigations
ERP/MRP systems
Coaching
Communication
Attention to detail

Education

High school diploma or equivalent
Associate's or Bachelor's degree (technical or life sciences)

Tools

ERP/MRP systems

Job description

Promed Molded Products Inc. is seeking a GMP Manufacturing Lead to ensure smooth, compliant production scheduling and disciplined documentation on the manufacturing floor in Plymouth, Minnesota.

The role coordinates the people, materials, and systems to execute batches right the first time, working cross-functionally with Quality, Materials, and Manufacturing to maintain compliance. The candidate will manage GMP scheduling, ERP/MRP material setup, operator training, and production record review,

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