ZipRecruiter

Log In

1

Gmp Compliance Jobs (NOW HIRING)

The Mint Dispensary

GMP Compliance Specialist

Murdock, FL · On-site

$55K - $60K/yr

This role supports the company's Compliance team by overseeing GMP adherence, managing supplier quality documentation, and assisting with BioTrack reporting. The ideal candidate is detail-oriented ...

WuXi Biologics

US GMP Compliance Head

Cranbury, NJ · On-site

$160K - $260K/yr

Job Title - US GMP Compliance Head Department - Quality Assurance Work Location - Cranbury NJ (On-site) Job Summary Reporting to QA Head of US & APAC, the US GMP compliance head will play a pivotal ...

synergy

Pharmaceutical GMP QA Specialist

Dallas, TX

Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical ...

synergy

Pharmaceutical GMP QA Specialist

Dallas, TX · On-site

Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical ...

synergy

Pharmaceutical GMP QA Specialist

Dallas, TX · On-site

Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical ...

Cogent Biosciences

Senior Manager, Quality Control GMP

$155K - $185K/yr

This role is a senior individual contributor within the Quality organization and is responsible for driving method lifecycle management, ensuring GMP compliance, and supporting release and stability ...

next page

Showing results 1-20

All JobsGmp Compliance Jobs

Gmp Compliance information

See salary details

$31.5K

$98.9K

$207.5K

How much do gmp compliance jobs pay per year?

As of Jul 27, 2026, the average yearly pay for gmp compliance in the United States is $98,949.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,500.00 and $115,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a GMP Compliance professional, and why are they important?

To thrive as a GMP Compliance professional, you need a strong understanding of Good Manufacturing Practices, regulatory guidelines, and quality assurance, typically supported by a degree in life sciences or a related field. Familiarity with quality management systems (QMS), audit processes, and relevant certifications such as Six Sigma or ISO standards is highly valued. Attention to detail, strong analytical thinking, and effective communication are essential soft skills for this role. These abilities ensure that manufacturing processes consistently meet regulatory requirements, safeguarding product quality and organizational reputation.

What does GMP compliance stand for?

GMP compliance stands for Good Manufacturing Practice compliance, which ensures that products are consistently produced and controlled according to quality standards. It is essential for jobs in pharmaceutical, biotech, and food manufacturing environments, often requiring knowledge of regulations, documentation, and quality assurance processes.

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

AspectGmp ComplianceQuality Assurance Specialist
CertificationsGMP Certification, Regulatory Compliance TrainingISO 9001, Quality Management System Training
Work EnvironmentPharmaceutical, biotech, or medical device manufacturingManufacturing, healthcare, or pharmaceutical industries
Employer & Industry UsageRegulatory agencies, pharmaceutical companiesManufacturers, quality departments

Gmp Compliance focuses on ensuring products meet Good Manufacturing Practice standards and regulatory requirements. Quality Assurance Specialists oversee overall quality systems, including GMP adherence, but also broader quality processes. While both roles require knowledge of GMP, Gmp Compliance is more specialized in regulatory adherence, whereas Quality Assurance covers a wider scope of quality management.

Will compliance be replaced by AI?

GMP compliance professionals oversee adherence to Good Manufacturing Practice regulations in the pharmaceutical and biotech industries. While AI tools can assist with data analysis, documentation, and monitoring, human expertise remains essential for interpreting regulations, making judgment calls, and ensuring overall compliance. AI is viewed as a support tool rather than a replacement for compliance roles.

What is GMP compliance?

GMP compliance refers to adhering to Good Manufacturing Practice (GMP) regulations, which are guidelines set by agencies like the FDA to ensure products are consistently produced and controlled according to quality standards. These practices cover all aspects of manufacturing, from raw materials to hygiene and staff training. GMP compliance is critical in industries such as pharmaceuticals, food, and cosmetics to ensure product safety and efficacy. Regular audits, documentation, and continuous improvement are essential parts of maintaining GMP compliance.

What are some common challenges faced by professionals working in GMP compliance roles?

Professionals in GMP (Good Manufacturing Practice) compliance often encounter challenges such as keeping up with evolving regulatory requirements, ensuring consistent implementation of procedures across all departments, and managing detailed documentation. They also work to foster a culture of quality and compliance among teams that may have varying levels of GMP knowledge. Additionally, GMP compliance specialists frequently collaborate with production, quality assurance, and regulatory affairs teams to coordinate audits, resolve non-conformities, and support continuous improvement efforts.

What is the highest paying job in compliance?

In compliance, senior roles such as Compliance Director or Chief Compliance Officer tend to be the highest paying, often earning six-figure salaries. These positions require extensive experience, leadership skills, and knowledge of regulations like GMP, FDA, or ISO standards.
More about Gmp Compliance jobs
What are the most commonly searched types of Gmp Compliance jobs? The most popular types of Gmp Compliance jobs are:
What states have the most Gmp Compliance jobs? States with the most job openings for Gmp Compliance jobs include:
What job categories do people searching Gmp Compliance jobs look for? The top searched job categories for Gmp Compliance jobs are:
Gmp Compliance jobs near you
Infographic showing various Gmp Compliance job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, and 5% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $98,949 per year, or $47.6 per hour.
GMP Compliance Manager (Devens, MA)

GMP Compliance Manager (Devens, MA)

CSI International

Tampa, FL • On-site

$80K/yr

Full-time

Posted 4 days ago

Job description

Who We Are

CSI International Inc, founded in 1989, provides integrated building services to clients in real estate, property management, pharmaceuticals, telecommunications, higher education, manufacturing, and insurance. Throughout CSI International Inc.’s constant growth and evolution, our primary goal – exceeding our clients’ expectations – has remained unchanged. Because of this, we enjoy an incomparable reputation for cost-effective solutions with responsive services with uncompromising quality.

What You Will Be Doing

The GMP Compliance Coordinator is responsible for supporting the quality, compliance, and documentation programs associated with GMP cleaning operations within a regulated pharmaceutical manufacturing environment. This position ensures that cleaning activities, employee training, documentation practices, and quality systems comply with current Good Manufacturing Practices (cGMP), site procedures, and client requirements. The GMP Compliance Coordinator serves as a key liaison between operations and quality stakeholders, helping maintain inspection readiness, regulatory compliance, and continuous improvement initiatives.

This position is located in Devens, MA.

GMP Compliance Manager Duties and Responsibilities

  • Monitor GMP cleaning operations to ensure compliance with cGMP regulations, site procedures, and client quality standards.
  • Identify, document, and assist in resolving compliance issues, deviations, non-conformances, and quality events.
  • Support internal audits, client audits, and regulatory inspections by preparing documentation, coordinating records, and responding to information requests.
  • Conduct routine inspections and compliance reviews to verify adherence to established cleaning and quality requirements.
  • Manage GMP cleaning documentation, including logbooks, training records, and controlled documents.
  • Review records for accuracy, completeness, and compliance with GDP and data integrity standards.
  • Maintain document control systems and coordinate document revisions and change-control activities.
  • Administer training programs and maintain qualification records.
  • Support root cause investigations and CAPA programs.
  • Analyze quality and compliance data and identify process improvements.
  • Prepare reports, compliance metrics, and KPI summaries.
  • Participate in operational, quality, and cross-functional meetings.
  • Serve as a point of contact for client quality representatives.

GMP Compliance Manager Requirements and Qualifications

  • Associate's degree or Bachelor's degree in a related field; equivalent experience may be substituted.
  • Minimum of 2 years of experience in a GMP-regulated environment.
  • Working knowledge of cGMP regulations, GDP, and data integrity principles.
  • Experience managing controlled documents, training records, compliance programs, or quality systems.
  • Familiarity with deviation investigations, CAPA processes, and root cause analysis.
  • Experience supporting audits or inspections preferred.
  • Familiarity with eQMS platforms such as Veeva, MasterControl, or TrackWise preferred.
  • Strong organizational, analytical, and communication skills.
  • Proficiency in Microsoft Office applications.
  • Ability to work within a regulated pharmaceutical manufacturing environment.
  • Authorized to Work in the US – We Use Everify.

CSI International, Inc. is committed to fostering, cultivating, and preserving a culture of diversity and inclusion. We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Our commitment extends beyond preventing discrimination and harassment; it’s about creating an environment where diverse backgrounds and perspectives are valued. We believe in the power of our people, the ideas they bring, and what we can accomplish together.

Consistent with the Americans with Disabilities Act (ADA), all state & federal requirements, it is the policy of CSI International, Inc. to provide reasonable accommodation when requested by a qualified applicant or employee with a disability, unless such accommodation would cause an undue hardship. CSI International, Inc. also provides reasonable accommodations as required under the Pregnant Workers Fairness Act (PWFA) for limitations related to pregnancy, childbirth, or related medical conditions. The policy regarding requests for reasonable accommodation applies to all aspects of employment, including the application process. If reasonable accommodation is needed, please contact the Recruitment Team at 813-425-1985.

#CSIHP


Wednesday - Sunday
2:00PM - 10:00PM