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Gmp Facility Manager Jobs (NOW HIRING)

Abzena Inc.

GMP Facility Services Associate

Bristol, PA · On-site

$18 - $25/hr

The associate works closely with Manufacturing, Quality Assurance, Materials Management, Warehouse ... GMP facility services. • Support internal audits, client audits, regulatory inspections ...

JLL

Senior Facility Manager

South San Francisco, CA · On-site

As a Senior Facility Manager, you'll serve as the strategic leader responsible for the ... Ensure GMP/GLP compliance through completion of all training, audit responses, and critical PMs on ...

JLL

Facility Manger

Waltham, MA · On-site

As a Facilities Manager, you will oversee operations in GMP certified facilities, focusing on pharmaceutical, food & beverage, or manufacturing industries. You'll report to the JLL Regional ...

JLL

Facility Manager

Holly Springs, NC · On-site

As a Facility Manager, you will oversee operations in GMP certified facilities, focusing on pharmaceutical manufacturing industries. You'll report to the JLL Regional Facilities Director and be ...

Compass Group

GMP FACILITIES MANAGER

Chesterfield, MO · On-site

$80K - $90K/yr

Position Title: GMP FACILITIES MANAGER Shift: 10 AM -7PM Salary: $80,000 - $90,000 Location ... In 2020, ESFM (formerly Eurest Services) won the George Graves Award for Facility Management ...

Amentum

Facility Manger

Richmond, VA · On-site

Bachelor's degree in Engineering, Business Administration, Facility Management, Industrial ... Experience working in a GMP or similar regulated environment. * Experience utilizing CMMS - Maximo ...

Pae

Facility Manger

Richmond, VA · On-site

Bachelor's degree in Engineering, Business Administration, Facility Management, Industrial ... Experience working in a GMP or similar regulated environment. * Experience utilizing CMMS - Maximo ...

Romark Logistics Of Pa Inc

Facility Manager

Cranberry, PA · On-site

$100 - $125/hr

The Facilities Manager is responsible for ensuring the safe, reliable, and efficient operation of ... Support compliance with food safety, GMP, and customer-specific requirements while protecting ...

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Gmp Facility Manager information

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$25K

$68.9K

$121K

How much do gmp facility manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for gmp facility manager in the United States is $68,936.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,000.00 and $84,500.00 per year, depending on experience, location, and employer.

What does a GMP Facility Manager do?

A GMP Facility Manager oversees the daily operations of manufacturing facilities that follow Good Manufacturing Practices (GMP). They ensure that all processes, equipment, and environments comply with regulatory standards to maintain product safety and quality. This role involves coordinating maintenance, training staff on compliance, managing audits, and implementing protocols for cleanliness and safety. GMP Facility Managers play a crucial part in preventing contamination and ensuring that products meet industry and government requirements.

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

To thrive as a GMP Facility Manager, you need comprehensive knowledge of Good Manufacturing Practice regulations, facility operations, and quality management, typically supported by a degree in life sciences, engineering, or a related field. Familiarity with quality management systems (QMS), facility monitoring software, and regulatory documentation platforms is essential, along with certifications like Six Sigma or Lean Manufacturing being advantageous. Strong leadership, problem-solving abilities, and effective communication distinguish top performers in this role. These skills and qualifications ensure regulatory compliance, operational efficiency, and the production of safe, high-quality products in highly regulated environments.

What are some key challenges faced by GMP Facility Managers, and how can they effectively address them?

GMP Facility Managers often face the challenge of maintaining strict regulatory compliance while overseeing daily operations and facility maintenance. Balancing production schedules with necessary equipment validations and inspections can be demanding, especially during audits or when implementing process changes. Effective communication with quality assurance, engineering, and production teams is essential to ensure everyone is aligned with compliance requirements. Proactively scheduling maintenance and fostering a culture of continuous improvement can help address these challenges and ensure smooth facility operations.

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

AspectGmp Facility ManagerQuality Assurance Specialist
Required CredentialsGMP certifications, facility management experienceGMP certifications, QA training
Work EnvironmentManufacturing plants, laboratoriesQuality control labs, manufacturing sites
Employer & Industry UsagePharmaceutical, biotech, biotech manufacturingPharmaceutical, biotech, medical device industries
Common Search & ComparisonYesYes

The Gmp Facility Manager oversees the operational aspects of GMP-compliant facilities, ensuring compliance and smooth functioning. The Quality Assurance Specialist focuses on maintaining product quality through testing and documentation. While both roles require GMP knowledge and certifications, the Facility Manager manages facility operations, whereas the QA Specialist emphasizes quality control processes.

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Gmp Facility Manager jobs near you
Infographic showing various Gmp Facility Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $68,936 per year, or $33.1 per hour.

GMP Facility Services Supervisor

Bristol, PA • On-site

Abzena Inc.
Manufacturing • 51 - 200 employees
Learn more about Abzena Inc.external

Full-time

Posted 7 days ago

Job description

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
The GMP Facility Supervisor is responsible for the day-to-day supervision of manufacturing operations personnel and activities within Abzena's current Good Manufacturing Practice (cGMP) production areas, as well as oversight of janitorial and site cleaning services. This role ensures that batch manufacturing, in-process testing support, equipment operation, facility cleanliness, and documentation practices are executed safely, on schedule, and in full compliance with cGMP requirements, approved batch records, SOPs, and applicable regulatory standards. The position serves as a frontline leader responsible for staffing, training, performance management, and shift-level execution of the production schedule.
The GMP Facility Supervisor collaborates closely with Quality Assurance, Quality Control, Validation, Engineering, Facilities, Supply Chain, and Manufacturing Science and Technology to ensure production areas, equipment, and personnel remain compliant, inspection-ready, and capable of consistently supporting GMP manufacturing operations.
Requirements
  • Supervise day-to-day GMP manufacturing operations to ensure production activities are performed safely, on schedule, and in full compliance with cGMP requirements and regulatory expectations.
  • Directly supervise, train, coach, mentor, and develop manufacturing operators and technicians, including scheduling, performance evaluations, hiring recommendations, and disciplinary/termination recommendations as needed.
  • Review and approve executed batch production records, logbooks, and associated GMP documentation for accuracy, completeness, and compliance, utilizing SAP, MES, or equivalent systems for batch close-out and reporting, prior to Quality Assurance release.
  • Ensure operators are trained and qualified on current SOPs, batch records, and equipment prior to performing GMP manufacturing activities.
  • Oversee shift staffing, work assignments, and production scheduling to meet manufacturing targets and client delivery timelines.
  • Serve as a key resource for troubleshooting manufacturing deviations, equipment malfunctions, and process issues encountered on the production floor.
  • Author, review, and revise SOPs, batch records, and work instructions to reflect current practices and continuous improvement initiatives.
  • Initiate, lead, and drive to closure deviation investigations, CAPAs, change controls, and root cause analyses related to manufacturing operations, in partnership with Quality Assurance.
  • Enforce safety, gowning, and cGMP behavioral standards within production areas, including cleanroom and controlled environment protocols, and maintain manufacturing areas to site 5S/6S cleanliness and organization standards.
  • Oversee janitorial services and site cleaning operations, including scheduling, quality checks, vendor/contractor coordination, and compliance with GMP cleaning and sanitation requirements across classified and non-classified areas.
  • Coordinate with Quality Assurance to support batch disposition, in-process quality checks, and real-time release activities.
  • Monitor and report key performance indicators such as batch yield, right-first-time, schedule adherence, and equipment downtime.
  • Support internal and client audits and regulatory inspections by providing manufacturing documentation, floor walkthroughs, and subject matter expertise.
  • Represent Manufacturing Operations in client meetings, project team calls, and technical discussions as the subject matter expert for assigned production processes.
  • Ensure proper use, cleaning, and maintenance of manufacturing equipment, including coordination of calibration and preventive maintenance activities with Engineering.
  • Manage material and component readiness, including staging, reconciliation, and accountability of GMP materials used in production.
  • Participate in technology transfer, process validation, and new product introduction activities as a manufacturing operations representative.
  • Identify and lead continuous improvement initiatives to enhance manufacturing efficiency, right-first-time performance, and operator engagement.
  • Serve as backup to the Manufacturing Manager/Associate Director as needed, including escalation of critical production and compliance issues to site leadership.

Physical Requirements
  • Ability to work in office, GMP manufacturing, cleanroom, warehouse, and utility environments.
  • Ability to wear required personal protective equipment (PPE) and cleanroom gowning for extended periods.
  • Ability to work occasional off-shift hours, weekends, or extended shifts to support production schedules.
  • Ability to sit, stand, walk, and utilize computer systems for extended periods.
  • Ability to lift up to 25 pounds occasionally.

Qualifications
  • Bachelor's degree in Life Sciences, Chemistry, Biology, Engineering, or related discipline required; equivalent education/experience combinations considered in lieu of degree (e.g., Associate's degree with 7+ years, or High School diploma/GED with 9+ years, of relevant GMP manufacturing experience), consistent with 21 CFR 211.25(b) supervisor qualification requirements.
  • Minimum 5 years of experience in GMP manufacturing operations (8+ years if without a qualifying degree), including at least 2 years in a formal or informal supervisory, lead, or shift-lead capacity, within a pharmaceutical, biotechnology, or related regulated manufacturing environment.
  • Strong working knowledge of cGMP regulations, FDA requirements, EU Annex guidelines, and data integrity principles.
  • Experience executing, reviewing, and approving batch production records, SOPs, and controlled GMP documentation.
  • Experience supporting deviations, CAPAs, change controls, audits, and regulatory or client inspections.
  • Strong leadership, coaching, and performance management skills with the ability to motivate and develop production teams.
  • Strong analytical, organizational, and problem-solving skills, with the ability to make sound decisions under time pressure.
  • Proficiency in Microsoft Office (Excel, Word, Outlook) and manufacturing execution systems (MES), CMMS, or ERP platforms.
  • Ability to communicate effectively across all levels of the organization, including cross-functional teams and site leadership.
  • Experience overseeing janitorial, custodial, or facility cleaning services, including vendor management, in a regulated or GMP environment preferred.
  • Experience with aseptic processing, biologics, or drug substance/drug product manufacturing preferred.

FLSA: Exempt
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.

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