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Gmp Manager Jobs (NOW HIRING)

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 ...

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 Services LP

GMP Tech

Concord, NC · On-site

$18.50 - $19/hr

GMP Tech The GMP Tech will be responsible for keeping assigned areas within GMP in clean and ... 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

Pearland, TX · On-site

$15.50 - $16.50/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

Windham, NY

$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

SBM Management

GMP Technician

Salisbury, NC

$18.50 - $19/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

Charlotte, NC

$18.50 - $19/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

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 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

Cairo, NY

$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

SBM Management

GMP Technician

Salisbury, NC

$18.50 - $19/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

Cairo, NY

$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

SBM Management

GMP Technician

Greenville, NY

$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

SBM Management

GMP Technician

Kannapolis, NC

$18.50 - $19/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

Pearland, TX

$15.50 - $16.50/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

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 ...

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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 Jun 28, 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.

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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Gmp Manager jobs near you
Manager GMP Quality Operations

Manager GMP Quality Operations

Vertex Pharmaceuticals

Boston, MA • On-site

$118K - $177K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 16 days ago

Job description

Job Description
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 will provide QA support of manufacturing operations for the external manufacture of Cell & Genetic Therapeutic programs. This role will drive, review, and support activities related to product disposition, including review of batch data, batch records, deviations, in-process data, EM data, QC release testing, and other quality systems documentation, while advancing intelligent digitized solutions for backlog triage, metrics generation, records reconciliation, and archiving to improve operational efficiency, compliance, and data integrity.
Key Duties & Responsibilities
  • Responsible for quality support of Vertex Cell and Gene Therapy manufacturing operations across all phases of development, support of analytical laboratory, materials management and manufacturing operations.

  • Support Quality System oversight across CDMOs, focusing on compliance, CAPA effectiveness, change control, and risk management in accordance with GxP and global quality standards

  • Develop and maintain quality metrics, dashboards, and reports in Python, Power BI and Smartsheet to provide clear visibility into QMS performance and process trends

  • Partner with External CDMOs to identify any operational efficiencies and drive implementation.

  • Responsible for identifying compliance risks and gaps for GMP processes and supporting implementation of mitigating controls

  • Support audit and inspection readiness activities.

  • Maintain periodic batch record metrics and assists department with routine/quarterly Quality System data review metrics and reporting

  • Develop intelligent digitized solutions for archiving and lifecycle management of GMP records to improve retrieval, traceability, compliance, and inspection readiness

  • Develop AI-enabled catch-up solutions to support backlog triage, prioritize quality records, and accelerate resolution of deviations, CAPAs, and batch disposition activities to improve overall Quality operations

  • Lead and participate in Cell & Genetic Program and Quality projects and drive continuous improvement activities.

  • Implement AI-supported records reconciliation solutions to identify discrepancies, improve data integrity, and enhance completeness and accuracy of GMP documentation across quality systems and manufacturing records

Required Knowledge/Skills
  • Bachelor's degree in a Business / Sciences field.

  • 5+ years of QA experience in a GMP-regulated environment

  • Hands-on experience with ATMPs (cell therapy, gene therapy, tissue-engineered products) strongly preferred or with Biologicals/sterile

  • Demonstrated AI skills and digital capability to design and deliver intelligent solutions that improve Quality operations, including backlog triage, metrics generation, records reconciliation, and archiving within a GMP-regulated environment, while supporting data integrity, compliance, and risk-based decision-making

  • Demonstrated experience providing QA support to GMP manufacturing operation

  • Experience with network-based applications such as Oracle, TrackWise, Veeva

  • Ability to evaluate quality metrics, strong problem solving and make decisions utilizing risk-based approach

  • Proven experience leading a variety of projects/teams within stated objectives and timelines

  • Ability to manage own workload to achieve goals and seek opportunities to share information and help others understand technical processes

  • Strong communication skills (written and verbal) with the ability to communicate effectively with cross functional team members, exchanging complex information and influencing/guiding others to understand a stated viewpoint

Pay Range:
$118,400 - $177,600
Disclosure Statement:
The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
Flex Designation:
On-Site Designated
Flex Eligibility Status:
In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time.
#LI-Onsite
Company Information
Vertex is a global biotechnology company that invests in scientific innovation.
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

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