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DivIHN

QA Contractor, GMP Quality Assurance

NC · On-site

QA Contractor, GMP Quality Assurance Location: Onsite at Research Triangle Park, NC Duration: 9 Months Travel: Domestic travel (less than 10% of the time) expected. Only W2 candidates are eligible ...

Jade Biosciences

Role Overview The Director, GMP Quality Assurance (QA) provides QA support across Jade's product pipeline across various stages of development. This role serves as a key partner to CMC and cross ...

PCCA

Quality Assurance Specialist

Houston, TX · On-site

Quality Assurance & GMP Compliance * Support compliance with Good Manufacturing Practices (GMP), internal procedures, and regulatory requirements. * Collaborate with department management to ...

Bimeda Inc.

QA Compliance Lead - Afternoons

Pomona, CA · On-site

Coach and mentor QA Compliance Associates on investigations, documentation, and GMP expectations. Partner cross-functionally with Operations, QC, and other teams to drive a culture of quality and ...

LeadStack Inc.

GMP QA Validation Specialist

Durham, NC · On-site

$45 - $53/hr

QA Validation Specialist Location: Research Triangle Park, NC - 27709 Duration: 10 Months Pay Rate: $45/hr - $53/hr on W2 The Validations Contractor - GMP Quality Assurance, reporting to the ...

LeadStack Inc.

GMP QA Validation Specialist

Durham, NC · On-site

$45 - $53/hr

QA Validation Specialist Location: Research Triangle Park, NC - 27709 Duration: 10 Months Pay Rate: $45/hr - $53/hr on W2 The Validations Contractor - GMP Quality Assurance, reporting to the ...

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How much do qa gmp jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for qa gmp in the United States is $23.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $24.28 per hour, depending on experience, location, and employer.

What is the difference between Qa Gmp vs Quality Assurance Specialist?

AspectQa GmpQuality Assurance Specialist
CertificationsGMP training, QA certificationsQA certifications, GMP knowledge often preferred
Work EnvironmentPharmaceutical, biotech, or medical device manufacturingVarious industries including pharma, food, and manufacturing
Employer & Industry UsageRegulated industries with strict compliance standardsBroadly used across multiple industries requiring quality assurance
Search & Comparison IntentUnderstanding GMP-specific QA rolesGeneral QA roles with GMP considerations

Qa Gmp professionals focus specifically on ensuring compliance with Good Manufacturing Practices in regulated industries like pharmaceuticals and biotech. Quality Assurance Specialists may work across various sectors, applying quality standards including GMP. While both roles require similar certifications and work in quality environments, Qa Gmp roles are more specialized in GMP compliance, whereas Quality Assurance Specialists have broader responsibilities across industries.

What is a QA GMP?

QA GMP jobs refer to positions in Quality Assurance (QA) that focus on ensuring compliance with Good Manufacturing Practices (GMP) in industries such as pharmaceuticals, biotechnology, and food production. Professionals in these roles are responsible for monitoring processes, conducting audits, and maintaining documentation to ensure that products are consistently produced and controlled according to quality standards. They play a critical role in safeguarding consumer safety and ensuring regulatory compliance. QA GMP specialists often coordinate with other departments to implement quality systems and handle non-conformances.

What skills and qualifications are needed to thrive as a QA GMP professional?

To thrive as a QA GMP professional, you need a solid understanding of GMP regulations, quality systems, and a background in life sciences or a related field. Familiarity with quality management software, audit tools, and regulatory documentation systems is typically required. Attention to detail, problem-solving abilities, and strong communication skills set outstanding candidates apart. These skills ensure compliance with regulatory standards, safeguard product quality, and support efficient manufacturing operations.

What are common challenges faced by QA GMP professionals in maintaining compliance within a manufacturing facility?

QA GMP professionals often encounter challenges such as keeping up with evolving regulatory standards, ensuring consistent documentation practices, and managing cross-departmental communication. They must be vigilant in identifying deviations or non-conformances and work closely with production, engineering, and quality control teams to implement corrective actions. Balancing day-to-day oversight with the need for ongoing training and audits can be demanding, but these activities are essential to uphold product quality and regulatory compliance.
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What cities are hiring for Qa Gmp jobs? Cities with the most Qa Gmp job openings:
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Qa Gmp jobs near you
Infographic showing various Qa Gmp job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 3% Part Time, 7% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $48,237 per year, or $23.2 per hour.

QA Contractor, GMP Quality Assurance

DivIHN

NC • On-site

Contractor

Re-posted 23 days ago

Job description

For further inquiries regarding the following opportunity, please contact our Talent Specialist, Hema at (630) 847-0275
Title:QA Contractor, GMP Quality Assurance
Location: Onsite at Research Triangle Park, NC
Duration: 9 Months
Travel: Domestic travel (less than 10% of the time) expected.
Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered
Description:
The QA Contractor, GMP Quality Assurance, reporting to the Manager, GMP Quality Assurance, or designee, will be responsible for assisting in the management of client Quality Management System (QMS) and will strongly support client's Culture of Quality. This role will assure corporate compliance with applicable GMP national, international, and state regulations. This position will be based at our headquarters facility in RTP, NC.
Job Responsibilities
  • Manage assigned day-to-day QA responsibilities in support of the company's Quality Management Systems (QMS).
  • Provide timely support of Learning Management System, Change Control, Deviation Management Systems, or other QMS based customer requests.
  • Liaison with applicable department record owners to ensure their complete and timely resolution. Review and Approve said record types as assigned.
  • Provide accurate and timely weekly and quarterly QMS metric and Key Performance Indicator updates to QA and CMC senior management.
  • Collaborate successfully with the other departments to ensure that direct and supportive tasks are completed within project timelines.
  • Providing deliverables and resolving issues; Draft SOPs/controlled documents as well as perform quality unit review and approval of Quality Management Systems requests/ records related to Learning Management, Non-Conformance Management, CAPA management, and metric/KPI reporting.
  • Continually evaluate systems and procedures for improvement for efficiency and compliance to applicable regulatory requirements and standards.
  • Participate in project meetings as a Quality Unit representative and support colleagues by acting as a technical resource for quality and compliance related issues.
  • Perform daily customer-facing activities, as assigned by area management.
  • Maintain health of customer-facing activities such as document archival activities and notebook/logbook assignment and management.
  • Identify and collaborate with colleagues to implement continuous improvement initiatives; provide Quality Unit oversight of QMS based activities.
  • Assist in the qualification and oversight of vendors, contract manufacturers, contract laboratories, and service providers.
  • Support regulatory (FDA, EMA) and internal audits/inspections per client procedures and applicable regulatory requirements.
  • Communicate project status to stakeholders and escalate issues in a timely manner.
  • Perform and support other duties as assigned by area management.

About you
  • Bachelor's degree in a scientific field and 4+ years of experience in GMP based Quality Assurance, particularly in support/oversight of a company QMS, or 10+ years of GMP based Quality Assurance experience using a company QMS.
  • 3+ experience working within a pharmaceutical/biotech Quality Management system, such as Trackwise, ZenQMS, Veeva, is a requirement
  • Strong understanding of GMP guidelines and Quality Systems with the ability to apply GMPs in conformance to U.S. standards, and where appropriate, other regulatory authority standards.
  • Ability to author, review, and interpret Standard Operating Procedures (SOPs).
  • Ability to identify and/or resolve quality issues/discrepancies with others in a proactive, diplomatic, flexible, and constructive manner.
  • Strong attention to detail, highly organized and the ability to multitask in a fast-paced, highly interactive environment.
  • Strong service-oriented mindset with excellent verbal and written communication skills, and the ability to effectively collaborate with peers including scientific/technical colleagues.
  • Experience in analytical method validation and QC testing, especially in the fields of mammalian cell culture and Gene Therapy/Biologics based potency testing, is preferred.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

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