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Remote Gmp Manufacturing Jobs (NOW HIRING)

Danaher

Senior Scientist - MSAT

Marlborough, MA · On-site +1

$92K/yr

You have demonstrable expertise in bioprocessing and GMP manufacturing. * You have experience ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Danaher

Business Development Manager

San Jose, CA · On-site +1

$145K - $175K/yr

... remote. You will be a part of the North American Sales Team and report to the Regional Sales ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

Danaher

Business Development Manager

Boston, MA · On-site +1

$145K - $175K/yr

... remote. You will be a part of the North American Sales Team and report to the Regional Sales ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

Danaher

Business Development Manager

Palo Alto, CA · On-site +1

$145K - $175K/yr

... remote. You will be a part of the North American Sales Team and report to the Regional Sales ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

Danaher

Business Development Manager

Oakland, CA · On-site +1

$145K - $175K/yr

... remote. You will be a part of the North American Sales Team and report to the Regional Sales ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

Danaher

Business Development Manager

Fremont, CA · On-site +1

$145K - $175K/yr

... remote. You will be a part of the North American Sales Team and report to the Regional Sales ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

Danaher

Business Development Manager

San Francisco, CA · On-site +1

$145K - $175K/yr

... remote. You will be a part of the North American Sales Team and report to the Regional Sales ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

Danaher

Business Development Manager

Sunnyvale, CA · On-site +1

$145K - $175K/yr

... remote. You will be a part of the North American Sales Team and report to the Regional Sales ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

CRB

Electrical Engineer IV

Raleigh, NC · Remote

Experience in GMP manufacturing environments, including life sciences or food & beverage facilities ... Remote CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal ...

CRB

Electrical Engineer IV

Omaha, NE · Remote

Experience in GMP manufacturing environments, including life sciences or food & beverage facilities ... Remote CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal ...

CRB

Electrical Engineer IV

Omaha, NE · Remote

Experience in GMP manufacturing environments, including life sciences or food & beverage facilities ... Remote CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal ...

CRB

Electrical Engineer IV

Raleigh, NC · Remote

Experience in GMP manufacturing environments, including life sciences or food & beverage facilities ... Remote CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal ...

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How much do remote gmp manufacturing jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for remote gmp manufacturing in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

What are some common challenges of working in a remote GMP manufacturing role, and how can they be addressed?

Working remotely in GMP (Good Manufacturing Practice) manufacturing presents unique challenges, such as ensuring strict compliance with regulatory standards without being physically present on-site. Communication with on-site teams is crucial to maintain oversight and address any deviations or quality concerns promptly. Leveraging digital tools, clear documentation, and regular virtual meetings can help bridge the gap. It’s also important to stay updated on the latest regulatory changes and maintain strong collaboration with quality assurance, production, and validation teams to ensure all processes are followed accurately.

What is the difference between Remote Gmp Manufacturing vs Remote Quality Assurance?

AspectRemote Gmp ManufacturingRemote Quality Assurance
CredentialsGMP certifications, technical manufacturing experienceGMP certifications, quality control certifications
Work EnvironmentManufacturing facilities, labs, or remote production oversightRemote review, audits, documentation, and compliance checks
Industry UsagePharmaceutical, biotech, and medical device manufacturingPharmaceutical, biotech, and medical device industries
Common Search IntentManufacturing processes, production oversightQuality compliance, audits, documentation

Remote Gmp Manufacturing focuses on overseeing and managing manufacturing processes remotely, ensuring production meets GMP standards. Remote Quality Assurance emphasizes maintaining quality compliance through remote audits, reviews, and documentation. Both roles require GMP certifications but differ in daily tasks and focus areas within the industry.

What are the key skills and qualifications needed to thrive as a remote GMP manufacturing professional?

To thrive as a Remote GMP Manufacturing professional, you need in-depth knowledge of Good Manufacturing Practices (GMP), quality control, and regulatory compliance, typically supported by a degree in life sciences or engineering. Familiarity with digital manufacturing systems, batch record management software, and possibly certifications like Six Sigma or GMP training is essential. Strong attention to detail, problem-solving skills, and effective remote communication set outstanding candidates apart. These skills ensure the integrity of product quality and regulatory compliance, even in a remote or decentralized work environment.

What is remote GMP manufacturing?

Remote GMP manufacturing refers to the oversight, management, or operation of Good Manufacturing Practice (GMP) compliant production processes from a location outside the actual manufacturing facility. This can involve remote monitoring of production data, quality control, and compliance activities using digital tools and secure communication platforms. The goal is to maintain high standards of product quality and regulatory compliance, even when staff or consultants are not physically present onsite. This approach has become more common due to advancements in technology and the increased need for flexibility in the pharmaceutical and biotechnology industries.
More about Remote Gmp Manufacturing jobs
What cities are hiring for Remote Gmp Manufacturing jobs? Cities with the most Remote Gmp Manufacturing job openings:
What are the most commonly searched types of Gmp Manufacturing jobs? The most popular types of Gmp Manufacturing jobs are:
What states have the most Remote Gmp Manufacturing jobs? States with the most job openings for Remote Gmp Manufacturing jobs include:
What job categories do people searching Remote Gmp Manufacturing jobs look for? The top searched job categories for Remote Gmp Manufacturing jobs are:
Remote Gmp Manufacturing jobs near you
Infographic showing various Remote Gmp Manufacturing job openings in the United States as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 3% In-person, and 97% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.

Manager, CMC Drug Substance

Albert B Sabin Vaccine Institute, Inc.

Remote

$109K - $130K/yr

Full-time

Posted yesterday

New

Job description

Reports to: Senior Manager, CMC
Location: Remote work, US Only
Why Sabin:
Our mission is to make vaccines more accessible, enable innovation and expand immunization across the globe. We seek a future free from vaccine-preventable diseases. We are an innovative, collaborative, and engaged team that values accountability, teamwork, partnership, and driving impact. We are vaccine champions improving lives through immunization. Sabin staff, management and the Board of Trustees are committed to ensuring that fairness, integrity, and opportunity remain at the core of how we operate.
Position Summary:
The Manager, CMC Drug Substance provides technical leadership and expertise across Chemistry, Manufacturing, and Controls (CMC) activities supporting vaccine drug substance development. This role focuses on process development, characterization, technology transfer, and GMP manufacturing, supporting programs from late-stage clinical development through process validation, regulatory licensure, and commercialization.
The successful candidate will possess demonstrated experience leading technology transfers across process development and manufacturing environments, with hands-on knowledge of vaccine manufacturing operations and viral vaccine platforms, including adenovirus-vectored vaccines or comparable systems. The individual will provide technical leadership for drug substance development and manufacturing activities, partnering closely with internal teams, contract development and manufacturing organizations (CDMOs), and external stakeholders to support process scale-up, validation, regulatory compliance, and commercial readiness. Success in this role requires strong cross-functional collaboration, sound scientific judgment, and a commitment to advancing vaccine access and global health impact.
Working closely with internal teams, contract development and manufacturing organizations (CDMOs), and external stakeholders, the Manager will drive project execution by coordinating technical activities, managing risks, and ensuring alignment with program objectives, timelines, and regulatory requirements. The role requires strong scientific and technical expertise, sound judgment, and the ability to work effectively across cross-functional teams.
The Manager, CMC Drug Substance will collaborate across CMC, clinical, regulatory, quality, and global health functions to advance vaccine programs through critical development milestones. The ideal candidate combines technical leadership, intellectual curiosity, and a commitment to expanding equitable access to vaccines and improving global health outcomes.
Key Responsibilities:
  • Support the planning, coordination, and execution of vaccine development programs from late-stage clinical development through regulatory submission and commercial supply, partnering with cross-functional scientific, analytical, regulatory, manufacturing, and global health stakeholders to achieve key milestones and timelines
  • Support site selection and onboarding of a new Drug Substance Site
  • Lead the tech transfer of a Phase 3 vaccine manufacturing process to external Drug Substance manufacturing partners, ensuring successful process scale-up, validation, and commercial readiness
  • Execute technology transfer strategies, project plans, governance structures, and risk mitigation plans to ensure successful transfer and lifecycle management of manufacturing processes
  • Lead process characterization, comparability assessments, scale-up/scale-down studies, and process validation activities to establish robust manufacturing processes and support regulatory submissions. Develop and maintain the Drug Substance process control strategy, including process parameter criticality assessments, critical process parameter (CPP) identification, critical in-process controls (cIPCs), and contribute to continued process verification (CPV) strategies
  • Author, review, and approve CMC technical documentation, including technology transfer packages, process characterization reports, validation documentation, regulatory submission content, comparability reports, and responses to Health Authority inquiries.
  • Drive project execution by managing technical deliverables, timelines, risks, and cross-functional dependencies, ensuring alignment with organizational priorities, regulatory requirements, and donor commitments.
  • Ensure compliance with cGMP, regulatory expectations, quality standards, and organizational procedures throughout process development, technology transfer, validation, and commercial manufacturing
  • Contribute to funding proposals, grant reporting, and strategic planning efforts to advance vaccine access and equity worldwide

Requirements
  • Bachelor's degree in biochemistry, chemistry, biology, chemical engineering or related pharmaceutical science
  • Minimum of 7+ years of experience in biopharmaceutical CMC, manufacturing, process development, and technology transfer
  • Demonstrated experience in biopharmaceutical manufacturing, MS&T, and/or process development environments, including hands-on experience with mammalian or viral cell culture, upstream and downstream processing, and purification operations (e.g., chromatography, filtration/ultrafiltration, viral clearance)
  • Prior technology transfer experience, including leading or supporting site-to-site, scale-up, or CDMO transfers
  • Experience with adenovirus-vectored vaccines or other viral vector platforms (e.g., AAV, poxvirus, lentiviral vectors) is strongly preferred; candidates with comparable complex biologics manufacturing experience will also be considered
  • Strong analytical, problem-solving, organizational, communication, and interpersonal skills, with the ability to work effectively both independently and collaboratively across cross-functional teams, global stakeholders, and diverse audiences
  • Commitment to health equity and improving immunization access in underserved populations

Preferred Skills and Experience:
  • Direct experience operating in cGMP-regulated environments, including support for non-conformance investigations, root cause analysis, change control, and CAPA implementation
  • Working knowledge of ICH guidelines and global regulatory requirements (e.g., FDA, EMA, MHRA), with experience supporting late-stage development programs, regulatory submissions (e.g., BLA/NDA), and commercial supply activities
  • Experience working with external manufacturing partners

Other:
  • Subject to a criminal background investigation
  • Request for three professional references
  • Verification of education/degrees
  • Travel up to 25%

Salary Description
$109,000 - $130,000

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