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Project Coordinator Gmp Jobs (NOW HIRING)

W3Global Inc.

Assistant Project Coordinator

Ontario, CA · On-site

$31 - $35/hr

Coordinate and oversee supplier GMP audits, social compliance audits, and quality assessments ... Identify project risks and implement proactive solutions to prevent delays or compliance issues.

FootBridge

Sr. Project Engineer

Lebanon, IN · On-site

$100K - $125K/yr

Strong experience with procurement, document control, material coordination, and project ... GMP/cGMP, cleanroom, or FDA-regulated facility experience. * Experience with Procore, Bluebeam ...

Phenx

WI · On-site

You're steering teams, balancing GMP and GAMP requirements with reality and keeping biotech ... Project Manager/Coordinator who's done the work, understands the pressure and still loves the game.

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How much do project coordinator gmp jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for project coordinator gmp in the United States is $28.81, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $33.17 per hour, depending on experience, location, and employer.

What is the difference between Project Coordinator Gmp vs Project Coordinator Pharmaceutical?

AspectProject Coordinator GmpProject Coordinator Pharmaceutical
CertificationsGMP compliance training, relevant project management certificationsGMP training, project management certifications
Work EnvironmentPharmaceutical manufacturing, quality assurance settingsPharmaceutical companies, drug development labs
Industry UsageCommonly used in GMP-regulated environmentsUsed across pharmaceutical projects, including GMP and non-GMP areas

The Project Coordinator Gmp and Project Coordinator Pharmaceutical roles share similar certifications and work environments, primarily within pharmaceutical manufacturing. However, the Project Coordinator Gmp specifically focuses on GMP compliance and quality standards, whereas the Project Coordinator Pharmaceutical may work across broader pharmaceutical projects, including non-GMP areas. Both roles are essential for ensuring project success in regulated environments.

Are project coordinator GMP jobs in demand?

Project Coordinator GMP jobs are in demand in industries such as pharmaceuticals and manufacturing, where compliance with Good Manufacturing Practices is essential. These roles often require knowledge of regulatory standards, project management skills, and familiarity with GMP guidelines, making them valuable in regulated environments with ongoing industry growth.

How much is the salary of a project coordinator?

The salary of a Project Coordinator varies depending on experience, location, and industry, but typically ranges from $50,000 to $75,000 annually. Certifications like PMP or experience with project management tools can influence compensation levels.

What is a typical day in a project coordinator GMP job?

A project coordinator GMP's typical day involves managing project schedules, coordinating communication between teams, and ensuring compliance with Good Manufacturing Practice regulations. They often use project management tools, review documentation, and monitor progress to meet deadlines and quality standards. The role requires strong organizational skills and attention to detail in a regulated environment.

What cities are hiring for Project Coordinator Gmp jobs?

Cities with the most Project Coordinator Gmp job openings:

What states have the most Project Coordinator Gmp jobs?

States with the most job openings for Project Coordinator Gmp jobs include:

What are popular job titles related to Project Coordinator Gmp jobs?

For Project Coordinator Gmp jobs, the most frequently searched job titles are:

Infographic showing various Project Coordinator Gmp job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 86% Full Time, 8% Part Time, and 4% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $59,915 per year, or $28.8 per hour.

Bilingual (English & Chinese) Project Coordinator/Manager - CDMO Service

Germantown, MD • On-site

uBriGene (MA) Biosciences Inc.
See more jobs at uBriGene (MA) Biosciences Inc.external

$60K - $100K/yr

Full-time

Re-posted 18 days ago

Job description

Position Summary:
We are seeking an individual with a strong background in viral vector production and/or project management.  This position reports to VP of Commercial Strategy
  • Provide project management support to CMC team members including PD, TT and GMP teams in their execution of activities including manufacturing and release of drug substance and drug product, manufacturing process improvements and validation, analytical method development, transfer and validation, and shipping studies.
  • Serve as the primary liaison between uBriGene and clients on CMC activities for the client projects. 
  • Collect updates on all CMC activities in the MS Project file on a monthly basis to update % completion or new dates.
  • Schedule, conduct, and draft minutes for PD, TT and GMP team on respective client projects to ensure regular, efficient team, and stakeholder communication.
  • Facilitate robust communication within PD, TT and GMP teams to ensure all functions are aware of the schedule, changes in strategy and impacts to risks and resources.
  • Hold team members accountable for on-time completion of tasks or milestones.
  • Performs critical path analysis and supports scenario planning for CMC deliverables.
  • Provide project coordination and communication, including participation in technical calls and face-to-face meetings, development of agendas, creation of meeting minutes, tracking of action items, and scheduling of follow-up meetings.
  • Support writing, review, and schedule of CMC related regulatory documents and health authority interactions.
  • Assist in preparing presentations, updating corporate project plans, etc.
  • Other responsibilities as needed

II. Requirements
Education, Experience, and Skills 
  • B.S. or MS. in engineering or biological sciences degree is required
  • > 3 years of experience in biologics manufacturing, preferably in viral vector production 
  • Previous project management experience in the biologics production is preferred but not required. 
  • Proven experience organizing, planning, and executing large-scale projects from vision through implementation
  • Experience using project management tools (project scheduling and resource management), such as MS Project. 
  • Proven analytical, conceptual and problem solving skills are required to evaluate business problems and apply knowledge to identify appropriate solutions. 
  • Exceptional team building and stakeholder relationship management skills are required, with the ability to establish rapport, persuade and effectively negotiate with senior management, key stakeholders and functions. 
  • Bilingual skills in English and Chinese are preferred. 

uBriGene Biosciences, Inc. is an equal employment opportunity employer and does not discriminate against any applicant on the basis of race, color, religion, sex, sexual orientation, gender expression and identity, national origin, ancestry, age, mental and physical disability, genetic information, any veteran status, military status or application for military service, or membership in any other category protected under applicable law.
 

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