ZipRecruiter

Log In

1

Gmp Writer Jobs (NOW HIRING)

Medasource

GMP Compliance Investigator

Durham, NC · On-site

This is a highly collaborative role for someone with strong GMP quality experience, exceptional technical writing skills, and the ability to manage complex investigations from initiation through ...

SBM Management Services LP

GMP Tech

Manvel, TX · On-site

$18 - $19/hr

GMP Tech Job Overview The GMP Tech will be responsible for keeping assigned areas within GMP in ... and written. The individual should be able to explain how to complete a task, using basic ...

SBM Management Services LP

GMP Tech

Manvel, TX · On-site

$18 - $19/hr

GMP Tech Job Overview The GMP Tech will be responsible for keeping assigned areas within GMP in ... and written. The individual should be able to explain how to complete a task, using basic ...

SBM Management Services LP

GMP Technician

Raritan, NJ · On-site

$19 - $20/hr

Title: GMP Technician Job Overview The GMP Tech will be responsible for keeping assigned areas ... and written. The individual should be able to explain how to complete a task, using basic ...

SBM Management Services LP

GMP Tech

Friendswood, TX · On-site

$18 - $19/hr

GMP Tech Job Overview The GMP Tech will be responsible for keeping assigned areas within GMP in ... and written. The individual should be able to explain how to complete a task, using basic ...

SBM Management Services LP

GMP Technician

Apex, NC · On-site

$21 - $22/hr

Title: GMP Technician Job Overview The GMP Tech will be responsible for keeping assigned areas ... and written. The individual should be able to explain how to complete a task, using basic ...

SBM Management Services LP

GMP Technician

Tipp City, OH · On-site

$15 - $16/hr

Title: GMP Technician Job Overview The GMP Tech will be responsible for keeping assigned areas ... and written. The individual should be able to explain how to complete a task, using basic ...

SBM Management Services LP

GMP Technician

Durham, NY · On-site

$16.50 - $17.50/hr

Title: GMP Technician Job Overview The GMP Tech will be responsible for keeping assigned areas ... and written. The individual should be able to explain how to complete a task, using basic ...

SBM Management Services LP

GMP Technician

Thurmont, MD · On-site

$20/hr

Title: GMP Technician Job Overview The GMP Tech will be responsible for keeping assigned areas ... and written. The individual should be able to explain how to complete a task, using basic ...

SBM Management Services LP

GMP Technician

Athens, GA · On-site

Title: GMP Technician Job Overview The GMP Tech will be responsible for keeping assigned areas ... and written. The individual should be able to explain how to complete a task, using basic ...

SBM Management Services LP

GMP Technician

Fajardo, PR · On-site

$10.50/hr

Title: GMP Technician Job Overview The GMP Tech will be responsible for keeping assigned areas ... and written. The individual should be able to explain how to complete a task, using basic ...

SBM Management Services LP

GMP Technician

Zebulon, NC · On-site

$16 - $17/hr

Title: GMP Technician Job Overview The GMP Tech will be responsible for keeping assigned areas ... and written. The individual should be able to explain how to complete a task, using basic ...

SBM Management Services LP

GMP Technician

Hillsboro, OR · On-site

$17.50 - $19/hr

Title: GMP Technician Job Overview The GMP Tech will be responsible for keeping assigned areas ... and written. The individual should be able to explain how to complete a task, using basic ...

previous pagenext page

Showing results 21-40

All JobsEducation JobsBusiness Education JobsTechnical Writer JobsGmp Writer Jobs

Gmp Writer information

See salary details

$13

$38

$66

How much do gmp writer jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for gmp writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

What are popular job titles related to Gmp Writer jobs?

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

Infographic showing various Gmp Writer job openings in the United States as of August 2026, with employment types broken down into 85% Full Time, 1% Part Time, 1% Temporary, 7% Contract, and 6% Nights. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.

GMP Compliance Investigator

Durham, NC • On-site

Medasource
Health Care and Social Assistance • 201 - 500 employees
Learn more about Medasourceexternal

Contractor

Posted 29 days ago

Job description

GMP Compliance Investigator - Equipment & Facilities
Overview
Our client is seeking a GMP Compliance Investigator - Equipment & Facilities to support a GMP manufacturing laboratory focused on advanced cellular therapies. This individual will play a key role in maintaining compliance with FDA regulations and applicable accreditation standards by leading investigations, authoring quality documentation, and partnering closely with Manufacturing and Quality teams.
This is a highly collaborative role for someone with strong GMP quality experience, exceptional technical writing skills, and the ability to manage complex investigations from initiation through closure.
Responsibilities
  • Develop, revise, and maintain Standard Operating Procedures (SOPs) to ensure compliance with FDA and applicable regulatory requirements.
  • Author and manage change controls related to SOP updates and manufacturing process improvements.
  • Edit batch records and manufacturing documentation as needed.
  • Initiate, investigate, author, and close deviations, CAPAs, investigations, and quality memos.
  • Partner with Manufacturing and Quality teams to investigate manufacturing events and drive timely closure of quality records.
  • Serve as the primary author for equipment and facility-related deviation investigations.
  • Attend meetings with equipment vendors and internal stakeholders to gather information supporting investigations.
  • Author validation documentation, including IQ, OQ, and PQ protocols, equipment assessments, and validation reports.
  • Manage deviation, CAPA, and change control timelines to support on-time batch release.
  • Perform failure mode analysis and root cause investigations.
  • Support batch release activities from a compliance perspective.
  • Ensure compliance with FDA regulations and applicable accreditation standards.
  • Train and educate personnel on updated procedures, SOPs, quality systems, and compliance requirements.
  • Assist during FDA, accreditation, sponsor, and regulatory inspections, including responses to audit observations.
  • Monitor Quality Agreements to ensure sponsor notification requirements are met.
  • Participate in continuous improvement initiatives to optimize quality systems and documentation processes.
Preferred Qualifications
  • Experience working in a Quality Assurance or GMP Compliance function within an FDA-regulated manufacturing environment.
  • Experience supporting deviations, investigations, CAPAs, and change controls.
  • Strong technical writing skills with experience authoring investigation reports and SOPs.
  • Experience participating in FDA inspections, regulatory audits, and sponsor audits.
  • Experience with electronic Quality Management Systems (QMS).
  • Project management experience.
  • Strong analytical and root cause investigation skills.
  • Excellent written and verbal communication skills.
  • Strong organizational skills with exceptional attention to detail.
  • Ability to work independently while collaborating effectively across cross-functional teams.
Minimum Qualifications
Education
  • Bachelor's degree in Biology, Life Sciences, or a related scientific discipline.

Experience
  • Minimum of 6 years of Quality Assurance, Quality Systems, or GMP Compliance experience within a regulated manufacturing environment.
  • A Master's degree in a related field may substitute for two years of experience.

Apply