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Gmp Manager Jobs (NOW HIRING)

GMP Pros

GMP Pros General Application

Omaha, NE · On-site

Project Management - General knowledge of project timelines and cost is important, but don't let ... GMP Pros is an Equal Opportunity Affirmative Employer (EEO/AA) and actively seeks to diversify its ...

Vrtx

Manager GMP Quality Operations

Boston, MA

$118K - $177K/yr

The GMP Quality Operations Manager is recognized internally as an expert in the principles and application of quality assurance, compliance, and AI-enabled quality operations. The Quality Manager ...

Global Channel Management

GMP Material Handler

Salisbury, NC · On-site

$15 - $18.25/hr

Trackwise Degree Lift 50lbs Proven understanding of cGMP M-F Flex to work OR/weekends PC savvy Prior GMP production, warehouse environs Statistical tools, analysis Inventory management systems (SAP ...

SBM Management

GMP Supervisor

Indianapolis, IN

$54K - $55K/yr

The GMP Supervisor will be responsible for coordinating activities within the assigned areas in the ... Correct at risk behavior immediately, then reports to the manager immediately * Provide ...

SBM Management

GMP Technician

Durham, NY · On-site

$17 - $18/hr

Description Position at SBM Management The GMP Tech will be responsible for keeping assigned areas within GMP in clean and orderly condition. The tech will work successfully with fellow employees and ...

SBM Management

GMP Technician

Concord, NC · On-site

$18.50 - $19/hr

Description Position at SBM Management The GMP Tech will be responsible for keeping assigned areas within GMP in clean and orderly condition. The tech will work successfully with fellow employees and ...

SBM Management

GMP Technician

Fremont, CA · On-site

$17.75 - $18.25/hr

Description Position at SBM Management The GMP Tech will be responsible for keeping assigned areas within GMP in clean and orderly condition. The tech will work successfully with fellow employees and ...

SBM Management

GMP Supervisor

Walkersville, MD · On-site

$60K - $60K/yr

Description Position at SBM Management The GMP Supervisor will be responsible for coordinating activities within the assigned areas in the GMP program. This includes the company employees and other ...

SBM Management

GMP Technician

Newark, CA

$17.75 - $18.25/hr

The GMP Tech will be responsible for keeping assigned areas within GMP in clean and orderly ... Communicate with lead, supervisor, co-workers, managers, and customers in a professional manner

SBM Management

GMP Technician

Portsmouth, NH · On-site

$20.50 - $21.50/hr

Description Position at SBM Management The GMP Tech will be responsible for keeping assigned areas within GMP in clean and orderly condition. The tech will work successfully with fellow employees and ...

SBM Management

GMP Technician

Indianapolis, IN · On-site

$17.15 - $18.15/hr

Description Position at SBM Management The GMP Tech will be responsible for keeping assigned areas within GMP in clean and orderly condition. The tech will work successfully with fellow employees and ...

SBM Management

GMP Supervisor

Indianapolis, IN · On-site

$54K - $55K/yr

Description Position at SBM Management The GMP Supervisor will be responsible for coordinating activities within the assigned areas in the GMP program. This includes the company employees and other ...

SBM Management

GMP Technician

Raritan, NJ · On-site

$20 - $23.60/hr

Description Position at SBM Management The GMP Tech will be responsible for keeping assigned areas within GMP in clean and orderly condition. The tech will work successfully with fellow employees and ...

SBM Management

GMP Technician

Portsmouth, NH

$20.50 - $21.50/hr

The GMP Tech will be responsible for keeping assigned areas within GMP in clean and orderly ... Communicate with lead, supervisor, co-workers, managers, and customers in a professional manner

SBM Management

GMP Technician

Bridgewater, NJ

$20 - $23.60/hr

The GMP Tech will be responsible for keeping assigned areas within GMP in clean and orderly ... Communicate with lead, supervisor, co-workers, managers, and customers in a professional manner

SBM Management

$17 - $18/hr

The GMP Tech will be responsible for keeping assigned areas within GMP in clean and orderly ... Communicate with lead, supervisor, co-workers, managers, and customers in a professional manner

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Gmp Manager information

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$24.5K

$59.5K

$116K

How much do gmp manager jobs pay per year?

As of Jul 21, 2026, the average yearly pay for gmp manager in the United States is $59,525.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,000.00 and $68,500.00 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.

Are GMP jobs in demand?

GMP (Good Manufacturing Practice) manager roles are in demand due to the ongoing need for compliance in pharmaceutical, biotech, and food manufacturing industries. These positions require knowledge of regulatory standards and quality assurance, and employment opportunities are often stable with industry growth. Certifications such as GMP training can enhance job prospects in this field.

What is a GMP manager?

A GMP manager oversees compliance with Good Manufacturing Practice (GMP) regulations in pharmaceutical, biotech, or food manufacturing facilities. They ensure production processes meet quality standards, often coordinating audits, training staff, and maintaining documentation to ensure product safety and efficacy.

What is a GMP job description?

A GMP Manager oversees compliance with Good Manufacturing Practice (GMP) regulations in pharmaceutical, biotech, or food manufacturing environments. They develop, implement, and monitor quality systems, ensure regulatory adherence, and conduct audits to maintain product safety and quality. Strong knowledge of industry standards, documentation skills, and relevant certifications are essential for this role.

What jobs pay $500,000 a year in the US?

High-level roles such as executive positions (CEO, CFO, COO), specialized medical professionals like neurosurgeons, and successful entrepreneurs can earn $500,000 or more annually. Certain senior management roles in large corporations, investment bankers, and top-tier lawyers also reach this income level, often requiring extensive experience, advanced skills, and professional certifications.

What are GMP Managers?

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.
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What cities are hiring for Gmp Manager jobs? Cities with the most Gmp Manager job openings:
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Gmp Manager jobs near you
Infographic showing various Gmp Manager job openings in the United States as of July 2026, with employment types broken down into 91% Full Time, 1% Part Time, 1% Temporary, 4% Contract, and 3% Nights. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $59,525 per year, or $28.6 per hour.
Senior Manager, GMP Quality

Senior Manager, GMP Quality

Revolution Medicines

Redwood City, CA • On-site

Full-time

Re-posted 17 days ago

Job description

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
Revolution Medicines is seeking a Senior Manager, GMP Quality who will play a key role within Quality Assurance and is responsible for providing leadership and operational GMP QA support for RevMed clinical programs, with a primary focus on clinical batch record review, product disposition, and release activities supporting global clinical trials.
Responsibilities:
  • Serve as the primary QA lead for clinical batch disposition activities, including comprehensive review and approval of executed batch records, deviations, investigations, and associated release documentation to ensure timely disposition of clinical trial materials.
  • Provide QA support for the manufacture, packaging, labeling, testing, storage, and release of clinical drug substance (DS), drug product (DP), and final product (FP) manufactured at CMOs and other GMP service providers.
  • Partner cross-functionally with Pharmaceutical Development & Manufacturing (PDM/CMC), Supply Chain, Regulatory Affairs, Clinical Operations, Analytical Development, and external CMOs to support uninterrupted supply of clinical trial materials.
  • Review and approve GMP documentation associated with clinical manufacturing and release activities, including master batch records, executed batch records, specifications, Certificates of Analysis, stability data, label proofs, shipping documentation, and analytical test results.
  • Collaborate with internal and external stakeholders to support quality systems and serve as QA SME for deviation investigations, CAPAs, change controls, product impact assessments, shelf-life extensions, and other GMP quality processes impacting clinical supply.
  • Ensure compliance with applicable global GMP regulations, ICH guidelines, company procedures, and industry best practices related to clinical manufacturing and release activities.
  • Support QA oversight of clinical manufacturing campaigns at CMOs, including on-site or remote support for manufacturing operations, batch review, and disposition activities as needed.
  • Drive continuous improvement initiatives to enhance batch review efficiency, release timelines, and overall effectiveness of GMP quality systems supporting clinical operations.
  • Review and approve GMP SOPs, work instructions, and controlled documents to ensure alignment with current regulatory expectations and company practices.
  • Support quality review of regulatory submissions and responses, including INDs/IMPDs and other clinical regulatory filings, as applicable.
  • Build positive professional relationships and foster a culture of quality, collaboration, accountability, and continuous improvement across internal teams and external partners.

Required Skills, Experience and Education:
  • A Bachelor's degree in a scientific or technical discipline is required.
  • A minimum of 8 years of experience in GMP Quality in the pharmaceutical industry, with experience in early to late-stage drug product development.
  • Excellent analytical skills and a strong technical background in small molecule process development, and testing are strongly desired.
  • Knowledge of applicable US and Global compliance regulations and industry practices.
  • Ability to critically evaluate and troubleshoot complex problems with diligence.
  • Strong teamwork, collaboration, and management skills.
  • Ability to manage multiple priorities and aggressive timelines.
  • Highly responsible, self-motivated professional with enthusiasm and passion for the work.
  • Highly proficient with various Microsoft and other computerized systems (e.g., Word, Outlook, Excel, PowerPoint, Visio, etc.).

Preferred Skills:
  • Hands-on experience working in a manufacturing environment overseeing QA responsibilities for commercial and late-stage programs is preferred.
    #LI-Hybrid #LI-JC1

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
Base Pay Salary Range
$164,000-$205,000 USD
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.
If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.

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