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Glp Qa Jobs (NOW HIRING)

Agenus, Inc.

Director, Quality Assurance

Lexington, MA · On-site

Lead the development, implementation, and continuous improvement of our GMP, GCP, and GLP quality ... Quality Assurance experience within the biotechnology or pharmaceutical industry, including ...

NCSL International

Director of GCP Quality

Princeton, NJ · On-site

$123.09 - $184.63/hr

About R&D Quality R&D Quality encompasses four teams GCLP/GLP Quality, PV Quality, Audit ... Furthermore, you will be taking up the role as GCP Inspection QA lead. The role requires profound ...

New

Legend Biotech USA

Director of GCP Quality

Princeton, NJ · On-site

$122.72 - $184.09/hr

About R&D Quality R&D Quality encompasses four teams GCLP/GLP Quality, PV Quality, Audit ... Furthermore, you will be taking up the role as GCP Inspection QA lead. The role requires profound ...

New

Frontage Laboratories

QA Manager

Exton, PA · On-site

Quality Assurance (QA) Specialist / Manager - DMPK Location: Exton, PA Department: DMPK (Drug ... Ensure compliance with GLP regulations, company SOPs, client requirements, and industry best ...

SystImmune, Inc

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

This role is responsible for ensuring compliance with Bioanalytical Lab QA (GLP/FDA) as well as CLIA/CAP requirements and partnering closely with scientific and laboratory teams to maintain a robust ...

Systimmune

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

This role is responsible for ensuring compliance with Bioanalytical Lab QA (GLP/FDA) as well as CLIA/CAP requirements and partnering closely with scientific and laboratory teams to maintain a robust ...

Neuralink

Quality Assurance Specialist

Austin, TX · On-site

$26.92 - $44.71/hr

Join the Quality Assurance Team, where our mission is to ensure compliance with relevant regulatory ... Conduct audits of Good Laboratory Practice (GLP) activities within Neuralink, and when needed ...

Bureau Veritas

$75K - $90K/yr

Expert knowledge of GLP, GMP, and regulatory frameworks Management & Leadership * Train and develop QA team on data analysis and quality management * Strong interpersonal and relationship-building ...

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Glp Qa information

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$38K

$118.1K

$179K

How much do glp qa jobs pay per year?

As of Aug 8, 2026, the average yearly pay for glp qa in the United States is $118,074.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $144,500.00 per year, depending on experience, location, and employer.

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

To excel as a GLP QA (Good Laboratory Practice Quality Assurance) professional, you should have a strong background in laboratory sciences, knowledge of GLP regulations, and experience with quality assurance processes. Familiarity with auditing tools, electronic data capture systems, and relevant certifications such as RQAP-GLP are often required. Excellent attention to detail, critical thinking, and strong communication skills are highly valued in this role. These competencies are essential to ensure compliance, accuracy, and integrity in non-clinical laboratory studies, which support regulatory submissions.

What is a GLP QA?

A GLP QA (Good Laboratory Practice Quality Assurance) job involves ensuring compliance with GLP regulations in a laboratory setting. GLP QA professionals monitor study procedures, audit data, and verify that documentation meets regulatory standards. Their role helps ensure the integrity, reliability, and consistency of non-clinical laboratory studies, often for regulatory submissions. They work closely with scientists, management, and regulatory agencies to uphold quality standards.

What does a GLP QA do?

As a GLP QA professional, your daily tasks may involve reviewing study protocols, conducting in-process and final audits, and ensuring that all laboratory processes comply with Good Laboratory Practice standards. You will work closely with laboratory staff, scientists, and management to identify and resolve compliance issues and participate in training initiatives. Additionally, documenting audit findings, preparing quality reports, and contributing to continuous improvement initiatives are common parts of the role. This position requires both independent review work and close collaboration with cross-functional teams to maintain the highest standards of data integrity and regulatory compliance.

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Glp Qa jobs near you
Infographic showing various Glp Qa 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 $118,074 per year, or $56.8 per hour.

QA/RA Specialist - Pharmaceutical GLP/GMP Experience

synergy

Dallas, TX • On-site

Full-time

Medical, Dental, Vision, PTO

Re-posted 15 days ago

Job description

QA/RA Specialist - Pharmaceutical GLP/GMP Experience

Synergy is seeking a knowledgeable and meticulous QA/RA Specialist with strong expertise in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) within the pharmaceutical industry. The specialist will be responsible for supporting the implementation, maintenance, and continuous improvement of quality and regulatory compliance systems to ensure adherence to FDA, EMA, and other regulatory requirements. This role involves reviewing procedures, ensuring documentation compliance, conducting internal audits, and assisting with regulatory submissions and inspections.

Key Responsibilities:

  • Develop, review, and maintain quality assurance and regulatory affairs documentation in compliance with GLP and GMP standards.
  • Ensure adherence to regulatory requirements from FDA, EMA, and other global regulatory agencies.
  • Conduct internal audits and inspections to assess compliance with quality systems and regulatory standards.
  • Support preparation and management of regulatory submissions and responses to regulatory agencies.
  • Collaborate with cross-functional teams to ensure compliance throughout product lifecycle.
  • Assist in training laboratory and manufacturing staff on quality system requirements and regulatory standards.
  • Investigate and support resolution of deviations, non-conformances, and CAPA activities.

Education & Experience:

  • Bachelor’s degree in life sciences, pharmacy, chemistry, or related field.
  • Minimum 5 years of experience in pharmaceutical GLP/GMP quality assurance and regulatory affairs.
  • Strong knowledge of FDA, EMA regulations, and ICH guidelines.
  • Experience with internal auditing and regulatory inspections.

Requirements

Education:

  • Bachelor’s degree in life sciences, pharmacy, chemistry, or a related discipline.

Experience:

  • At least 5 years of hands-on experience in pharmaceutical GLP/GMP QA and regulatory affairs.
  • Familiarity with international regulatory frameworks including FDA, EMA, and ICH guidelines.
  • Proven experience conducting internal audits and supporting regulatory inspections.

Skills:

  • Strong attention to detail and organizational skills.
  • Excellent communication and interpersonal abilities.
  • Ability to work collaboratively with cross-functional teams and manage multiple priorities.
  • Proficiency in quality management systems and documentation practices.

Benefits

  • Health Care Plan (Medical, Dental & Vision)
  • Paid Time Off (Vacation, Sick & Public Holidays)
  • Training & Development