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Gcp Qa Jobs in Raleigh, NC (NOW HIRING)

Syntricate Technologies

DevOps Engineer

Cary, NC · On-site

$51.75 - $71/hr

... GCP knowledge would be a great advantage Company : Syntricate Technologies offers quality assurance, validation, regulatory, business analysis, and project management services. Founded in 2004, the ...

Linuxcareers

Build Programmer

Cary, NC · On-site

$110 - $170/hr

You will partner with engineering, QA, production, and infrastructure teams to create reliable ... Familiarity with cloud infrastructure (AWS, Azure, or GCP) and administering Windows-based build ...

Ruri Software Technologies LLC

Azure DevOps

Raleigh, NC · On-site

$49.25 - $67.50/hr

Collaborate with development, QA, and architecture teams to integrate DevOps best practices ... GCP) Soft Skills Strong problem-solving and analytical skills Excellent communication and cross ...

Segment (Twilio)

Technical Support Engineer

Raleigh, NC · On-site

$60 - $80/hr

The Technical Support Engineer (TSE) works closely with Development, QA, Operations, Customer ... Knowledge of Cloud Platforms AWS, Azure, and GCP user management. * Experienced with packet capture ...

New

RXinsider LTD.

Senior Clinical Project Manager

Raleigh, NC · On-site

$140 - $200/hr

Ensures all clinical trials are executed in compliance with ICH/GCP guidelines/regulations and applicable SOPs: participates in the planning of quality assurance activities and coordinates resolution ...

Aerogen

Clinical Trial Manager

Morrisville, NC · On-site

$90 - $120/hr

... Regulations, quality standards including GCP/ICH requirements, and Aerogen Pharma SOPs ... Assurance. * Participate in the identification, evaluation, and selection of clinical trial sites.

New

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Data Management & Quality Assurance * Collect, enter, review, and maintain research data with a ... Knowledge of clinical research regulations, Good Clinical Practice (GCP), and human subject ...

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Gcp Qa information

See Raleigh, NC salary details

$36.9K

$114.8K

$174K

How much do gcp qa jobs pay per year?

As of Sep 4, 2026, the average yearly pay for gcp qa in Raleigh, NC is $114,777.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,700.00 and $140,500.00 per year, depending on experience, location, and employer.

What is a GCP QA?

A GCP QA (Good Clinical Practice Quality Assurance) job involves ensuring compliance with regulatory guidelines in clinical research. Professionals in this role conduct audits, review protocols, and ensure clinical trials adhere to industry standards such as FDA and ICH guidelines. They work to identify, report, and mitigate risks to maintain the integrity of clinical data. GCP QA specialists collaborate with regulatory agencies, clinical teams, and sponsors to ensure ethical and quality-driven research practices.

What are the typical responsibilities of a GCP QA throughout a clinical trial?

GCP QA professionals are responsible for planning, conducting, and documenting quality audits of clinical trial processes, ensuring compliance with Good Clinical Practice guidelines and regulatory requirements. They review study documentation, identify compliance gaps, and work closely with clinical project teams to implement corrective actions. GCP QA specialists regularly communicate with sponsors, investigators, and regulatory agencies. Their oversight ensures data integrity and subject safety throughout the clinical trial lifecycle, which is vital for successfully bringing new therapies to market.

What are the key skills and qualifications needed to thrive in the GCP QA position, and why are they important?

To thrive as a GCP QA, you need a strong understanding of Good Clinical Practice (GCP) guidelines, clinical research processes, and quality assurance methodologies, often backed by a degree in life sciences or a related field. Experience with audit tools, electronic data capture (EDC), and certifications such as RQAP-GCP or similar are highly advantageous. Excellent attention to detail, communication skills, and the ability to work collaboratively stand out as essential soft skills. These capabilities ensure compliance, data integrity, and the smooth execution of clinical trials within regulatory frameworks.

What are the most commonly searched types of Gcp Qa jobs in Raleigh, NC?

The most popular types of Gcp Qa jobs in Raleigh, NC are:

What are popular job titles related to Gcp Qa jobs in Raleigh, NC?

For Gcp Qa jobs in Raleigh, NC, the most frequently searched job titles are:

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Gcp Qa jobs near you
Infographic showing various Gcp Qa job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 6% Part Time, 5% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $114,777 per year, or $55.2 per hour.

Systems Manager, Digital Quality

Oxford Biomedica

Durham, NC • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Join Us in Changing Lives
At OXB, our people are at the heart of everything we do. We're on a mission to enable life-changing therapies to reach patients around the world-and we're looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful.
Following the expansion of our US footprint with the acquisition of a new commercial-scale viral vector facility in Durham, North Carolina we have some new opportunities to join us.
We're currently recruiting for a Manager, Digital Quality Systems to join our Quality team. In this role, you will provide leadership and oversight for the quality and compliance of computerized and software systems, across all phases of the System Development Life Cycle. You will serve as the site Subject Matter Expert, for digital quality and data integrity, ensuring adherence to GxP requirements, corporate digital governance programs, and regulatory expectations, playing a key part in advancing our mission and making a real difference.
Please note this is a full time role, based on site in Durham, NC.
Your responsibilities in this role would be:
    • Provide quality oversight for computerized and software systems, across the SDLC.
    • Review and approve SDLC documentation, change controls, validation plans, URS, FRS, and related artifacts.
    • Oversee deviations, CAPAs, and continuous improvement activities associated with computerized systems.
    • Lead site initiatives to align, harmonize, and standardize digital systems governance with corporate programs (e.g., SDLC, Data Integrity, Risk Management, Periodic Reviews).
    • Act as the site Data Integrity steward
    • Maintain all digital systems in a state of inspection readiness.
    • Present and defend digital quality and data integrity programs and associated verification artifacts during client audits and regulatory inspections.
    • Support internal audits, customer audits, and regulatory inspections.
    • Provide guidance to SMEs and site stakeholders on maintaining compliant and inspection-ready digital systems.
    • Serve as liaison between site functions (Tech Ops, QA, Validation) and central dQ/DI functions.
    • Represent the site in quality leadership forums, site Quality Review Board, and corporate governance boards to adopt corporate digital quality and DI standards.
    • Establish, monitor, and report on site-based dQ/DI KPIs to site and corporate leadership.
    • Lead/assist with vendor audits and oversee risk-based digital system validation assessments.

We are Looking For:
  • Bachelor's degree or higher in IT, Computer Systems, Life Sciences, Engineering, or a related field.
  • Minimum of 5-7 years in the pharmaceutical/biotechnology industry, including IT compliance, digital quality, or computerized systems.
  • Hands-on experience implementing and managing GxP-compliant computerized system quality programs (COTS and custom systems).
  • Demonstrated experience designing and enforcing data integrity controls in computerized systems.
  • Experience managing high-performance teams and influencing cross-functional stakeholders.
  • Familiarity with AI/ML, automation, and next-generation laboratory platforms is a plus.
  • Comprehensive knowledge of global GMP regulations and guidance, including FDA, EU, ICH, GLP, GDocP, GDP, and GCP.
  • Strong experience in reviewing and approving system life cycle documentation, validation plans, change controls, and other digital quality artifacts.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the United States.
About Us:
OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 30 years of experience in viral vectors; the driving force behind the majority of gene therapies.
OXB collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXB's world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.
Why Join Us?
  • Competitive total reward packages
  • Wellbeing programs that support your mental and physical health
  • Career development opportunities to help you grow and thrive
  • Supportive, inclusive, and collaborative culture
  • State-of-the-art labs and manufacturing facilities
  • A company that lives its values: Responsible, Responsive, Resilient, Respect

We want you to feel inspired every day. At OXB, we're future-focused and growing fast. We succeed together-through passion, commitment, and teamwork.
Ready to Make a Difference?

Apply