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Manufacturing Gmp Coordinator Jobs (NOW HIRING)

Jobtailor

Principal Engineer - Global MSAT

Redmond, WA · On-site

Experience authoring regulatory CMC documents, coordinating responses to health authority questions ... Biologics Manufacturing * GMP Concepts * Regulatory Submissions * Process Lifecycle Management

Hologic

Manufacturing Data Coordinator

Marlborough, MA · On-site

$46K - $69K/yr

Manufacturing Data Coordinator Why Hologic Hologic empowers people to live healthier lives ... Communicate and reinforce Good Manufacturing Practices (GMP) to manufacturing personnel to uphold ...

Hologic

Manufacturing Data Coordinator

Marlborough, MA · On-site

$46K - $69K/yr

Manufacturing Data Coordinator Why Hologic Hologic empowers people to live healthier lives ... Communicate and reinforce Good Manufacturing Practices (GMP) to manufacturing personnel to uphold ...

Hologic

Manufacturing Data Coordinator

Marlborough, MA · On-site

$46K - $69K/yr

Manufacturing Data Coordinator Why Hologic Hologic empowers people to live healthier lives ... Communicate and reinforce Good Manufacturing Practices (GMP) to manufacturing personnel to uphold ...

5th HQ

Plant Coordinator

Miramar, FL

$20 - $22/hr

We are seeking a Plant Coordinator to join our pharmaceutical manufacturing team in Miramar, FL ... Knowledge of GMP regulations and safety procedures is a plus

Automated Systems, Inc.

GMP Technical Writer

Madison, WI · On-site

$50 - $70/hr

... manufacturing site in the Greater Madison Area. This role will support backlog closure across ... project coordination. * Relevant experience supporting engineering organizations, particularly ...

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Manufacturing Gmp Coordinator information

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How much do manufacturing gmp coordinator jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for manufacturing gmp coordinator in the United States is $22.99, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $25.48 per hour, depending on experience, location, and employer.

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Infographic showing various Manufacturing Gmp Coordinator job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 4% Part Time, 3% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $47,816 per year, or $23 per hour.

Senior Scientist, Technology Transfer & CDMO Operations

San Diego, CA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago

Job description

Summary
  • Lead end-to-end technology transfer and CDMO relationship management for radiopharmaceutical drug products, serving as the primary operational/technical liaison between internal teams and external CDMOs. Oversee the full CDMO lifecycle (selection/onboarding through clinical supply chain management) in alignment with Regulatory, Quality, and Clinical teams.
Responsibilities
  • Own technology transfer from internal development to domestic/international CDMOs (plans, timelines, success criteria).
  • Manage day-to-day CDMO relationships; resolve technical/operational issues; ensure quality, compliance, and delivery.
  • Oversee clinical supply chain (material flow, inventory, logistics, drug substance/product coordination).
  • Partner cross-functionally (Regulatory, Quality, Clinical) and communicate risks/status.
  • Lead agreements and documents (CDAs, Quality Agreements, Technical Packages, SOWs, supply agreements).
  • Develop technical transfer packages (process descriptions, batch records, analytical methods, specs, CMC documentation).
  • Support IND/CMC and quality activities (audits, gap assessments, CAPAs).
  • Maintain oversight through Phase 1+ (batch record reviews, deviations, change control, supply planning).
  • Support vendor qualification/RFP and due diligence.
  • Manage multiple concurrent projects (plans, risk registers, communication cadence).
  • Author and maintain program documentation; provide status reporting.
  • Travel up to 25–30%.
Education/Experience
  • BSc +7 years, MSc +5 years, or PhD +2 years in relevant scientific/engineering field with pharma/biopharma industry experience.
Preferred Qualifications
  • 5+ years direct tech transfer/CMC/manufacturing experience (pharma/biopharma/radiopharma).
  • Experience managing CDMOs across multiple geographies (ex-US strongly preferred).
  • IND-enabling and Phase 1 clinical manufacturing experience.
  • Radiopharmaceutical manufacturing/GMP familiarity.
  • Supply chain/clinical logistics experience preferred.
Skills/Qualifications
  • Working knowledge of CMC principles, GMP manufacturing, analytical method transfers, quality systems.
  • CDMO/vendor management; clinical supply chain knowledge (forecasting, logistics, cold chain, import/export considerations).
  • Document authoring (Quality Agreements, CDAs, Technical Packages, SOWs, regulatory CMC).
  • Strong project management (e.g., MS Project/Smartsheet; PMP a plus).
  • Cross-functional collaboration; clear written/verbal communication.
  • Regulatory awareness (FDA and international agencies).
  • Ethics/confidentiality; proactive problem-solving.
Benefits (if applicable)
  • Health coverage (medical/pharmacy/dental/vision), wellbeing programs, 401(k), disability/life insurance, and paid time off.
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