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Gmp Manager Jobs in Virginia (NOW HIRING)

GMP Recycle Tech

Altavista, VA · On-site

$15 - $16/hr

Title: GMP Recycle Tech Job Overview The GMP Recycle Technician is responsible for the recycle ... Talk with lead, supervisor, co-workers, managers, and customers in a professional manner * Maintain ...

GMP Recycle Tech

Altavista, VA · On-site

$15 - $16/hr

Title: GMP Recycle Tech Job Overview The GMP Recycle Technician is responsible for the recycle ... Talk with lead, supervisor, co-workers, managers, and customers in a professional manner * Maintain ...

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Showing results 1-20

Gmp Manager information

See Virginia salary details

$24.3K

$59K

$115K

How much do gmp manager jobs pay per year?

As of Aug 8, 2026, the average yearly pay for gmp manager in Virginia is $59,014.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,600.00 and $67,900.00 per year, depending on experience, location, and employer.

What is the difference between Gmp Manager vs Quality Assurance Manager?

AspectGmp ManagerQuality Assurance Manager
CertificationsGMP certifications, Quality Management certificationsISO 9001, Quality Management certifications
Work EnvironmentPharmaceutical, biotech, or medical device manufacturingVarious industries including manufacturing, healthcare, and food
Employer & Industry UsageRegulated industries with strict compliance standardsBroadly used across multiple industries for quality oversight
Primary FocusEnsuring compliance with Good Manufacturing PracticesOverseeing overall quality assurance processes

The Gmp Manager primarily focuses on ensuring compliance with Good Manufacturing Practices in regulated industries like pharmaceuticals and biotech. In contrast, the Quality Assurance Manager oversees broader quality assurance processes across various industries. Both roles require similar certifications and work environments but differ in their specific compliance and quality scope.

What is a GMP manager?

GMP Managers are professionals responsible for ensuring that manufacturing processes in industries such as pharmaceuticals, biotechnology, and food production comply with Good Manufacturing Practice (GMP) regulations. They oversee quality control, develop and implement standard operating procedures, and conduct internal audits to maintain regulatory standards. Their role is crucial for ensuring that products are consistently produced and controlled according to quality standards, thereby safeguarding consumer health and safety.

What are some common challenges faced by a GMP manager in maintaining regulatory compliance, and how are they typically addressed?

A GMP Manager often encounters challenges such as keeping up with evolving regulatory standards, ensuring consistent staff training, and managing thorough documentation. To address these, managers implement regular training programs, conduct internal audits to identify gaps, and foster a culture of quality across teams. Staying proactive about changes in regulations and collaborating with cross-functional teams helps ensure ongoing compliance and smooth inspections.

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

To thrive as a GMP Manager, you need in-depth knowledge of Good Manufacturing Practices, quality assurance, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with quality management systems (QMS), audit tools, and relevant certifications such as Six Sigma or ISO standards is typically required. Strong leadership, problem-solving abilities, and effective communication are vital soft skills for managing teams and ensuring adherence to regulations. These skills and qualifications ensure product safety, regulatory compliance, and continuous improvement within manufacturing processes.
What cities in Virginia are hiring for Gmp Manager jobs? Cities in Virginia with the most Gmp Manager job openings:
Infographic showing various Gmp Manager job openings in Virginia as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $59,014 per year, or $28.4 per hour.

EHS Manager (GMP experience required)

Granules Pharmaceuticals

Chantilly, VA • On-site

$95K - $115K/yr

Full-time

Re-posted 26 days ago


Job description

Job Type
Full-time
Description
Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!
With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.
We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.
We are seeking a highly experienced EHS Manager to lead and oversee Environmental, Health, and Safety (EHS) programs across our pharmaceutical operations in Chantilly and Manassas, Virginia. This role is responsible for ensuring full regulatory compliance, minimizing risk, and driving a strong safety culture across both sites.
Key Responsibilities
  • Manage and oversee all EHS programs for the Chantilly and Manassas manufacturing sites
  • Develop, implement, and continuously improve safety policies, procedures, and site-specific safety plans.
  • Ensure compliance with OSHA, FDA, EPA, GMP, and applicable state and local regulations
  • Lead site risk assessments, job hazard analyses, and safety audits
  • Investigate incidents, near-misses, and safety concerns; implement corrective and preventive actions (CAPA)
  • Oversee chemical safety, hazardous material handling, waste management, and emergency response programs
  • Plan and deliver safety training for employees, contractors, and visitors
  • Track, analyze, and report safety performance metrics; recommend improvement initiatives
  • Serve as the primary contact for regulatory inspections, audits, and external agencies
  • Partner with operations, quality, and engineering teams to integrate safety into daily activities and project.
  • Support GMP environments by ensuring safe manufacturing practices without compromising product quality

Requirements
Required Qualifications
  • Bachelor's degree in occupational health & safety, Environmental Science, Engineering, or related field.
  • Minimum 5-7 years of EHS or safety management experience in a pharmaceutical, biotech, or regulated manufacturing environment.
  • Strong working knowledge of OSHA, FDA, GMP, EPA, and industrial safety regulations.
  • Experience managing multi-site operations preferred.
  • Professional certifications such as CSP, ASP, NEBOSH, or equivalent strongly preferred.
  • Excellent leadership, communication, and organizational skills.
  • Ability to travel regularly between Chantilly and Manassas sites.

What We Offer
  • Competitive salary and comprehensive benefits package.
  • Opportunity to lead safety programs across multiple pharmaceutical sites.
  • Collaborative, quality-driven work environment.
  • Career growth and long-term stability.

We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.
Salary Description
$95,000 - $115,000/Yearly