ZipRecruiter

Log In

1

Gmp Compliance Jobs (NOW HIRING)

Lonza

LSA QA Sr. Compliance Specialist

Portsmouth, NH · On-site

$84K - $115K/yr

Serve as a subject matter expert for Quality Systems, GMP Compliance, and inspection readiness activities across the site * Lead and facilitate Quality Review Boards, including Deviation Review Board ...

5TH HQ STAFFING

Be Seen First

Quality Control Manager (English/Spanish)

Miramar, FL · On-site

$90K - $110K/yr

This position is responsible for overseeing laboratory operations, supervising QC personnel, ensuring GMP compliance, and maintaining the highest quality standards throughout the manufacturing ...

Dyne Therapeutics

Director, QA GMP Operations

Waltham, MA · On-site

$188K - $230K/yr

The Director of QA GMP Operations is responsible for management of GMP quality within our external ... Adjudicate on compliance discussions and negotiate any required corrective actions. * Create and ...

CEDENT

Quality Compliance Manager

Saranac Lake, NY · On-site

This position is responsible for ensuring a state of continuous GMP compliance of Client's services and activities. This requires a combination of regulatory knowledge, attention to detail, effective ...

Amgen SA

Quality Compliance, Director

Holly Springs, NC · On-site

$180 - $240/hr

Expertise in GMP compliance, inspection readiness, and regulatory requirements. * Experience with drug product manufacturing and compliance. What you can expect of us As we work to develop treatments ...

Jobtailor

Facilities & Maintenance Engineer

Caguas, PR · On-site

$90 - $130/hr

Maintain FDA, ISO 13485, GMP, and QMS compliance and audit readiness * Support IQ/OQ/PQ, requalification, calibration coordination, and change control activities * Diagnose complex equipment and ...

RoslinCT US

Senior Compliance Specialist

Hopkinton, MA

$90K - $124K/yr

Serve as the Operations compliance subject matter expert, supporting GMP manufacturing and operational activities across the site. * Drive timely and effective execution of quality system activities ...

previous page

Showing results 41-60

All JobsBusiness 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 Aug 22, 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 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 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 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.

Who is responsible for GMP compliance?

GMP compliance is primarily the responsibility of quality assurance and quality control teams within a company, with oversight from management. These professionals ensure manufacturing processes meet regulatory standards through audits, documentation, and training, often requiring knowledge of Good Manufacturing Practices and relevant certifications.
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 August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $98,949 per year, or $47.6 per hour.

LSA QA Sr. Compliance Specialist

Lonza

Portsmouth, NH • On-site

$84K - $115K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical

Job description

LSA QA Sr. Compliance Specialist
Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 7:00 AM-4:00 PM EST.
What you will get:
Below you will find a comprehensive summary of the benefits package we offer:
  • Performance-related bonus.
  • Medical, dental and vision insurance.
  • 401(k) matching plan.
  • Life insurance, as well as short-term and long-term disability insurance.
  • Employee assistance programs.
  • Paid time off (PTO).

Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.
What you will do:
The Sr. QA Compliance Specialist serves as a key member of the Quality Assurance organization and acts as a subject matter expert for Quality Systems and GMP Compliance. This role is responsible for driving inspection readiness, strengthening quality systems, and promoting a strong quality culture across the site. The successful candidate will partner cross-functionally with Manufacturing, QC, Validation, Engineering, and site leadership to ensure compliance with regulatory requirements and continuous improvement of quality processes.
  • Serve as a subject matter expert for Quality Systems, GMP Compliance, and inspection readiness activities across the site
  • Lead and facilitate Quality Review Boards, including Deviation Review Board, CAPA Review Board, Change Control Board, and Quality Council meetings
  • Review and approve deviations, investigations, CAPAs, change controls, SOPs, and other quality records to ensure compliance with internal procedures and regulatory requirements
  • Identify compliance gaps, process improvements, and risk mitigation opportunities while driving effective corrective and preventive actions
  • Support internal audits, customer audits, and regulatory inspections, including coordinating and authoring audit responses and commitments
  • Generate, trend, and communicate Quality Metrics, KPIs, and KQIs to support management review and continuous improvement initiatives
  • Provide GMP guidance, coaching, and training to cross-functional teams while promoting a sustainable culture of quality and compliance
  • Effectively manage multiple priorities and support site initiatives, special projects, and other duties as assigned

What we are looking for:
  • Bachelor's degree in Life Sciences, Chemistry, Biology, Engineering, or a related scientific discipline preferred
  • Minimum 5+ years of experience in Quality Assurance, Compliance, or Quality Systems within a GMP-regulated pharmaceutical or biotechnology environment
  • Strong knowledge of cGMP regulations, including FDA 21 CFR Parts 210/211, EU GMP Annex 1, and applicable ICH guidelines
  • Demonstrated experience managing deviations, CAPAs, change controls, investigations, and quality risk assessments
  • Experience supporting regulatory inspections, customer audits, and inspection readiness activities in a manufacturing environment
  • Strong analytical, organizational, and critical-thinking skills with the ability to make sound quality and compliance decisions
  • Excellent written and verbal communication skills, including technical writing and cross-functional collaboration abilities
  • Experience with electronic Quality Management Systems (eQMS) such as TrackWise, Veeva, MasterControl, or similar systems preferred

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.

What Lonza employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply