GMP Quality Assurance Consultant - Cell & Gene Therapy Location: Boston, MA Duration: Long Term Job Overview We are seeking an experienced GMP Quality Assurance Consultant to provide quality ...
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GMP Quality Assurance Consultant - Cell & Gene Therapy Location: Boston, MA Duration: Long Term Job Overview We are seeking an experienced GMP Quality Assurance Consultant to provide quality ...
Senior Director / Director - CMC/GMP Quality Assurance
Palo Alto, CA · On-site
$235K - $285K/yr
The GMP QA candidate will report to the Chief Technical Officer, Chemistry, Manufacturing and Controls, Regulatory CMC, and Quality Assurance. The GMP QA FTE candidate will support and work with ...
Senior Director / Director - CMC/GMP Quality Assurance
Palo Alto, CA · On-site
$235K - $285K/yr
The GMP QA candidate will report to the Chief Technical Officer, Chemistry, Manufacturing and Controls, Regulatory CMC, and Quality Assurance. The GMP QA FTE candidate will support and work with ...
Responsibilities Role Summary Quality Assurance Associate independently performs tasks with minimal ... Issuance of GMP documents i.e. logbooks, notebooks, batch records, etc. * Release of cleanrooms ...
Responsibilities Role Summary Quality Assurance Associate independently performs tasks with minimal ... Issuance of GMP documents i.e. logbooks, notebooks, batch records, etc. * Release of cleanrooms ...
Role Summary Quality Assurance Associate independently performs tasks with minimal supervision ... Issuance of GMP documents i.e. logbooks, notebooks, batch records, etc. * Release of cleanrooms ...
Role Summary Quality Assurance Associate independently performs tasks with minimal supervision ... Issuance of GMP documents i.e. logbooks, notebooks, batch records, etc. * Release of cleanrooms ...
QA Associate
Pomona, CA · On-site
Job Title: QA Associate (Quality Assurance) Location: Pomona, CA (In-office) Position Type ... Administer and maintain GMP documents (Policies, Corporate SOPs) and quality records within ZenQMS ...
QA Associate
Pomona, CA · On-site
Job Title: QA Associate (Quality Assurance) Location: Pomona, CA (In-office) Position Type ... Administer and maintain GMP documents (Policies, Corporate SOPs) and quality records within ZenQMS ...
Senior Director / Director - CMC/GMP Quality Assurance
Palo Alto, CA · On-site
$235K - $285K/yr
The GMP QA candidate will report to the Chief Technical Officer, Chemistry, Manufacturing and Controls, Regulatory CMC, and Quality Assurance. The GMP QA FTE candidate will support and work with ...
Senior Director / Director - CMC/GMP Quality Assurance
Palo Alto, CA · On-site
$235K - $285K/yr
The GMP QA candidate will report to the Chief Technical Officer, Chemistry, Manufacturing and Controls, Regulatory CMC, and Quality Assurance. The GMP QA FTE candidate will support and work with ...
... Quality Assurance Associate. This position, in the Manufacturing Quality Assurance department ... Responsibilities include performing GMP review of manufacturing records and data, review and ...
Quick apply
... Quality Assurance Associate. This position, in the Manufacturing Quality Assurance department ... Responsibilities include performing GMP review of manufacturing records and data, review and ...
Responsibilities Role Summary Quality Assurance Associate independently performs tasks with minimal ... Issuance of GMP documents i.e. logbooks, notebooks, batch records, etc. * Release of cleanrooms ...
Responsibilities Role Summary Quality Assurance Associate independently performs tasks with minimal ... Issuance of GMP documents i.e. logbooks, notebooks, batch records, etc. * Release of cleanrooms ...
... Quality Assurance Associate. This position, in the Manufacturing Quality Assurance department ... Responsibilities include performing GMP review of manufacturing records and data, review and ...
Quick apply
... Quality Assurance Associate. This position, in the Manufacturing Quality Assurance department ... Responsibilities include performing GMP review of manufacturing records and data, review and ...
Vruxxxxxx - Quality Assurance Associate Job Profile in Jersey City, NJ * Quality Assurance ... with GMP/GLP practices, analytical techniques, documentation, and quality systems. I am detail ...
Vruxxxxxx - Quality Assurance Associate Job Profile in Jersey City, NJ * Quality Assurance ... with GMP/GLP practices, analytical techniques, documentation, and quality systems. I am detail ...
QA Associate
Pomona, CA · On-site
$82K - $113K/yr
Job Title: QA Associate (Quality Assurance) Location: Pomona, CA (In-office) Position Type ... Administer and maintain GMP documents (Policies, Corporate SOPs) and quality records within ZenQMS ...
QA Associate
Pomona, CA · On-site
$82K - $113K/yr
Job Title: QA Associate (Quality Assurance) Location: Pomona, CA (In-office) Position Type ... Administer and maintain GMP documents (Policies, Corporate SOPs) and quality records within ZenQMS ...
Associate Director/Director, GMP QA & Compliance About Climb: Climb Bio is a clinical-stage biotechnology company developing therapeutics for patients with immune-mediated diseases. Our product ...
Associate Director/Director, GMP QA & Compliance About Climb: Climb Bio is a clinical-stage biotechnology company developing therapeutics for patients with immune-mediated diseases. Our product ...
Associate Director, Quality Assurance (GMP QC Lab Oversight) Reports to: Head of Quality Assurance Operations Location: Camarillo, CA (On-site) Classification: Exempt Overview: The Associate Director ...
Associate Director, Quality Assurance (GMP QC Lab Oversight) Reports to: Head of Quality Assurance Operations Location: Camarillo, CA (On-site) Classification: Exempt Overview: The Associate Director ...
Associate Director, Quality Assurance (GMP QC Lab Oversight) Reports to: Head of Quality Assurance Operations Location: Camarillo, CA (On-site) Classification: Exempt Overview: The Associate Director ...
Associate Director, Quality Assurance (GMP QC Lab Oversight) Reports to: Head of Quality Assurance Operations Location: Camarillo, CA (On-site) Classification: Exempt Overview: The Associate Director ...
Associate Director/Director, GMP QA & Compliance About Climb: Climb Bio is a clinical-stage biotechnology company developing therapeutics for patients with immune-mediated diseases. Our product ...
Associate Director/Director, GMP QA & Compliance About Climb: Climb Bio is a clinical-stage biotechnology company developing therapeutics for patients with immune-mediated diseases. Our product ...
QA Associate
Pomona, CA · On-site
Pomona, CA,United States | Full-time regular Job Title: QA Associate (Quality Assurance) Location ... Administer and maintain GMP documents (Policies, Corporate SOPs) and quality records within ZenQMS ...
QA Associate
Pomona, CA · On-site
Pomona, CA,United States | Full-time regular Job Title: QA Associate (Quality Assurance) Location ... Administer and maintain GMP documents (Policies, Corporate SOPs) and quality records within ZenQMS ...
Senior Specialist, GMP Quality Assurance
Waltham, MA · On-site
$89K - $122K/yr
The Senior Specialist, GMP Quality Assurance will collaborate internally with QA, RA, and CMC departments. As needed, work with external Approved Service Providers to ensure oversight and compliance.
Senior Specialist, GMP Quality Assurance
Waltham, MA · On-site
$89K - $122K/yr
The Senior Specialist, GMP Quality Assurance will collaborate internally with QA, RA, and CMC departments. As needed, work with external Approved Service Providers to ensure oversight and compliance.
Job Title: QA Associate (Quality Assurance) Location:Pomona, CA (In-office) Position Type:Full-time ... Administer and maintain GMP documents (Policies, Corporate SOPs) and quality records within ZenQMS ...
Job Title: QA Associate (Quality Assurance) Location:Pomona, CA (In-office) Position Type:Full-time ... Administer and maintain GMP documents (Policies, Corporate SOPs) and quality records within ZenQMS ...
Pomona, CA,United States | Full-time regular Job Title: QA Associate (Quality Assurance) Location ... Administer and maintain GMP documents (Policies, Corporate SOPs) and quality records within ZenQMS ...
Pomona, CA,United States | Full-time regular Job Title: QA Associate (Quality Assurance) Location ... Administer and maintain GMP documents (Policies, Corporate SOPs) and quality records within ZenQMS ...
Associate Director/Director, GMP QA & Compliance About Climb: Climb Bio is a clinical-stage biotechnology company developing therapeutics for patients with immune-mediated diseases. Our product ...
Associate Director/Director, GMP QA & Compliance About Climb: Climb Bio is a clinical-stage biotechnology company developing therapeutics for patients with immune-mediated diseases. Our product ...
Gmp Qa Associate information
See salary details
$12.98 - $17.44
17% of jobs
$18.91 is the 25th percentile. Wages below this are outliers.
$17.44 - $21.90
24% of jobs
The median wage is $24.13 / hr.
$21.90 - $26.35
18% of jobs
$26.35 - $30.81
15% of jobs
$31.18 is the 75th percentile. Wages above this are outliers.
$30.81 - $35.27
10% of jobs
$35.27 - $39.73
8% of jobs
$39.73 - $44.19
5% of jobs
$44.19 - $48.65
3% of jobs
$48.65 - $53.10
0% of jobs
$53.10 - $57.56
0% of jobs
$57.56 - $62.02
0% of jobs
$12
$29
$62
How much do gmp qa associate jobs pay per hour?
As of Sep 11, 2026, the average hourly pay for gmp qa associate in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.
What are popular job titles related to Gmp Qa Associate jobs?
For Gmp Qa Associate jobs, the most frequently searched job titles are:
GMP Quality Assurance Consultant - Cell & Gene Therapy
Boston, MA • On-site
Stark Pharma Solutions Inc
Contractor
Re-posted 7 days ago
Job description
Position: GMP Quality Assurance Consultant – Cell & Gene Therapy
Location: Boston, MA
Duration: Long Term
Job Overview
We are seeking an experienced GMP Quality Assurance Consultant to provide quality oversight and compliance support for Cell & Gene Therapy manufacturing operations, validation, laboratory, engineering, and capital projects in a GMP-regulated environment.
Key Responsibilities
- Provide GMP QA oversight for manufacturing operations, validation, analytical laboratories, and engineering activities.
- Review and support Change Controls, Validation Protocols, Risk Assessments, GMP Investigations, and CAPA.
- Support equipment qualification, calibration, preventive maintenance, and laboratory operations.
- Review equipment, facility, and utility trending programs.
- Support environmental monitoring (EM), routine testing, and facility control systems.
- Collaborate with cross-functional teams to ensure GMP compliance and timely issue resolution.
Required Qualifications
- 5–8+ years of GMP Quality Assurance experience in pharmaceutical, biotechnology, or Cell & Gene Therapy environments.
- Experience supporting GMP manufacturing operations, validation, and capital projects.
- Strong knowledge of GMP, QA, CAPA, Root Cause Analysis, Change Control, Risk Assessments, and aseptic processing.
- Experience with Veeva, Nuvolo, ViewLinc, or similar quality management systems.
- Bachelor's degree in Engineering, Life Sciences, or a related field (Master's preferred).
- Excellent communication, analytical, and problem-solving skills.