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Remote Vaccine Manufacturing Jobs (NOW HIRING)

Lukos

VAERS Clinician

Atlanta, GA · On-site +1

... vaccine manufacturers, government agencies, and other partners. For the VAERS Clinician position ... Work Location Remote (onboarding will occur at the CDC in Atlanta, GA) About Lukos Lukos delivers ...

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Remote Vaccine Manufacturing information

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How much do remote vaccine manufacturing jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for remote vaccine 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 is remote vaccine manufacturing?

Remote vaccine manufacturing refers to the process of producing vaccines at a facility that can be operated, monitored, or managed from a different location using digital technologies. This setup allows experts and technicians to oversee manufacturing processes, troubleshoot issues, and ensure quality control without being physically present at the production site. Remote vaccine manufacturing helps increase efficiency, expand access to expertise, and maintain production even when in-person presence is limited, such as during pandemics or in remote areas.

What are some common challenges faced by professionals working in remote vaccine manufacturing roles?

Professionals in remote vaccine manufacturing often encounter challenges such as coordinating effectively with cross-functional teams spread across different locations and time zones. Ensuring strict compliance with Good Manufacturing Practices (GMP) and maintaining quality control can be more complex when operations are decentralized. Additionally, remote roles may require increased reliance on digital tools and strong communication skills to monitor production processes and resolve issues promptly. Adapting to evolving regulatory requirements and troubleshooting technical problems without on-site support are also frequent hurdles.

What are the key skills and qualifications needed to thrive in remote vaccine manufacturing, and why are they important?

To thrive in Remote Vaccine Manufacturing, you need a solid background in biotechnology or pharmaceutical production, often supported by a degree in life sciences or engineering. Familiarity with Good Manufacturing Practices (GMP), automation systems like SCADA, and quality control protocols is essential. Strong problem-solving skills, attention to detail, and effective remote communication set top performers apart in this field. These competencies ensure safe, compliant, and efficient vaccine production, even when working off-site or managing distributed teams.

What is the difference between Remote Vaccine Manufacturing vs Remote Pharmaceutical Manufacturing?

AspectRemote Vaccine ManufacturingRemote Pharmaceutical Manufacturing
CredentialsRelevant certifications in vaccine production, quality control, and GMP standardsCertifications in pharmaceutical production, quality assurance, and GMP standards
Work EnvironmentLaboratory settings, production facilities, or remote quality monitoringLaboratory or production environments, with remote oversight or data analysis
Industry UsagePrimarily in vaccine development and production companiesBroader pharmaceutical companies, including drug manufacturing and biotech firms
Search & Comparison IntentOften compared due to similar manufacturing processes and certificationsRelated but broader, less specific to vaccines

Remote Vaccine Manufacturing focuses on the production and quality control of vaccines, requiring specialized certifications and working in labs or production facilities. Remote Pharmaceutical Manufacturing covers a wider range of drug production, including vaccines, but also other pharmaceuticals, with similar credentials. Both roles involve remote oversight, but vaccine manufacturing is more specialized in immunization products.

More about Remote Vaccine Manufacturing jobs

What cities are hiring for Remote Vaccine Manufacturing jobs?

Cities with the most Remote Vaccine Manufacturing job openings:

What states have the most Remote Vaccine Manufacturing jobs?

States with the most job openings for Remote Vaccine Manufacturing jobs include:

What job categories do people searching Remote Vaccine Manufacturing jobs look for?

The top searched job categories for Remote Vaccine Manufacturing jobs are:

Remote Vaccine Manufacturing jobs near you
Infographic showing various Remote Vaccine Manufacturing job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 4% Part Time, 3% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% 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 27 days ago

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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