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Remote Biologics Manufacturing Jobs (NOW HIRING)

Managed Staffing

Biocompatibility Scientist

FL · Remote

$145 - $150/hr

Remote (Client HQ: Gainesville, FL - No relocation required) Job Summary We are seeking an ... Lead biological safety assessments per ISO 10993 standards , providing scientific justification and ...

Lonza

Associate Director Business Development

Portsmouth, NH · On-site +1

$150K - $200K/yr

This role is fully remote, offering flexibility to work from any location with reliable internet ... Strong understanding of biologics drug development, manufacturing, and commercialization processes ...

Lonza

Associate Director Business Development

Portsmouth, NH · On-site +1

$150K - $200K/yr

This role is fully remote, offering flexibility to work from any location with reliable internet ... Strong understanding of biologics drug development, manufacturing, and commercialization processes ...

Lonza

Associate Director Business Development

Boston, MA · On-site +1

$150K - $200K/yr

Fully Remote We are seeking an Associate Director of Business Development to drive growth across ... Strong understanding of biologics drug development, manufacturing, and commercialization processes ...

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Remote Biologics Manufacturing information

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How much do remote biologics manufacturing jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for remote biologics 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 biologics manufacturing?

Remote biologics manufacturing refers to the production and oversight of biological drugs or therapies (like vaccines, monoclonal antibodies, or cell therapies) using digital technologies that allow staff to monitor, manage, and sometimes control manufacturing processes from off-site locations. This approach leverages tools such as data analytics, automation, and cloud-based systems to facilitate real-time monitoring and decision-making. Remote manufacturing can increase efficiency, reduce on-site staff requirements, and enable rapid response to issues, while maintaining strict quality and regulatory standards. It is especially valuable in global operations, where expertise and oversight are needed without geographical limitations.

How does working remotely in biologics manufacturing impact collaboration with on-site teams?

In remote biologics manufacturing roles, effective communication and collaboration with on-site teams are crucial. Typically, remote employees participate in regular virtual meetings, use project management software, and collaborate on documentation to stay aligned with laboratory and production staff. While you may not be physically present during hands-on processes, you’ll often provide support in areas such as process optimization, data analysis, and compliance from a distance. Building strong relationships with on-site colleagues and being proactive in communication can help overcome the challenges of remote coordination.

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

To thrive in Remote Biologics Manufacturing, you need a solid background in biotechnology, chemical engineering, or a related field, often supported by a relevant degree and manufacturing experience. Familiarity with process control systems, automation software (such as SCADA), and adherence to Good Manufacturing Practices (GMP) are typically required. Strong problem-solving, attention to detail, and effective remote communication skills help professionals excel in coordinating production activities from a distance. These competencies ensure safe, compliant, and efficient biologics production while maintaining high product quality and effective team collaboration remotely.

What is the difference between Remote Biologics Manufacturing vs Remote Biologics Quality Control?

AspectRemote Biologics ManufacturingRemote Biologics Quality Control
Primary RoleOversees production processes, equipment, and manufacturing workflows for biologicsEnsures product quality through testing, analysis, and compliance with standards
Required CertificationsBiotech manufacturing certifications, GMP trainingQuality assurance certifications, GMP and GLP training
Work EnvironmentLaboratory, cleanroom, or manufacturing facilities (remote oversight possible)Laboratory and testing environments (remote monitoring possible)
Industry UsageUsed by biotech and pharmaceutical companies during production phasesUsed during quality assurance, testing, and compliance checks

Remote Biologics Manufacturing focuses on overseeing the production of biologic drugs, ensuring manufacturing processes run smoothly. Remote Biologics Quality Control emphasizes testing and verifying product quality. Both roles require GMP knowledge and are integral to biologics development, often working closely but with distinct responsibilities.

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

Remote Biologics Manufacturing jobs near you
Infographic showing various Remote Biologics 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.

Senior Manager, Quality Chemistry Manufacturing and Controls (CMC) Drug Product (DP)

Albert B Sabin Vaccine Institute, Inc.

Remote

$135K - $165K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 days ago

Job description

Reports to: Director, Quality 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 Senior Manager, Quality CMC DP serves as primary Quality representative supporting vaccine DP manufacturing from clinical development through late-stage development, Process Performance Qualification (PPQ) readiness, licensure preparation, and commercialization. The role provides current Good Manufacturing Practices (cGMP) quality oversight for external DP manufacturing, aseptic processing, fill-finish operations, technology transfer, process validation, PPQ, commercial readiness, inspection readiness, and product disposition activities.
This position partners with CMC and Regulatory Affairs and external manufacturing organizations to ensure compliant manufacture, testing, release, and lifecycle management of vaccine DP in accordance with global cGMP requirements and regulatory expectations. The successful candidate will possess extensive DP quality experience supporting technology transfer, process validation, PPQ execution, health authority interactions, and commercialization readiness while ensuring manufacturing systems and quality processes remain compliant, scalable, and inspection ready.
Key Responsibilities:
  • Serve as primary Quality representative, providing cGMP oversight and risk-based quality decision-making across clinical and late-stage DP activities.
  • Provide Quality oversight for clinical manufacturing, engineering runs, technology transfer, scale-up activities, process validation, and PPQ readiness.
  • Participate in manufacturing readiness reviews and provide Quality approval for validation, media fills, PPQ execution, and commercial readiness activities.
  • Review batch records, deviations, investigations, analytical and stability data, environmental monitoring results, and change controls to support product disposition decisions.
  • Approve deviations, Corrective and Preventative Actions (CAPAs), change controls, risk assessments, and quality records supporting compliant operations.
  • Provide Quality oversight of Contract Development Manufacturing Organizations (CDMOs) and contract laboratories, including supplier qualification, audits, inspection support, and CAPA implementation.
  • Support preparation of quality documentation and responses associated with Biological License Application (BLA), Marketing Authorization Application (MAA), and other regulatory submissions.
  • Support regulatory inspections, including the Food and Drug Administration (FDA) inspections, Bioresearch Monitoring (BIMO) inspections, and Pre-Approval Inspections (PAIs).
  • Lead the development, implementation, and continuous improvement of Sabin's Quality Management System, quality governance, and sponsor oversight processes to support the organization's transition to a fully compliant global Marketing Authorization Holder (MAH).

Requirements
  • Bachelor's or advanced degree in scientific discipline.
  • 9+ years of Quality experience supporting biologics, vaccines, or pharmaceutical DP manufacturing.
  • Proven experience supporting technology transfer, process validation, PPQ execution, manufacturing readiness, and commercial launch preparation.
  • Demonstrated experience providing Quality oversight of aseptic manufacturing and fill-finish CDMOs.
  • Experience supporting FDA inspections, BIMO inspections, and/or PAIs.
  • Strong knowledge of 21 CFR Parts 210 and 211, Annex 1, ICH Q10, and global cGMP requirements applicable to sterile drug product manufacturing.
  • Experience supporting BLA, MAA, or equivalent regulatory submissions preferred.
  • Occasional travel required to support organizational alignment and business needs.

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

Sabin's philosophy is to ensure fair, unbiased, equitable, competitive compensation and benefits. Using benchmarking and salary survey data, the annual salary for this position ranges from $135,000 - $165,000. The exact compensation may vary based on skills, experience, training, and certifications/degree. As a grant-funded organization, Sabin actively seeks funding for existing and new programs.
Sabin provides a comprehensive benefits package that includes medical, dental, and vision coverage, as well as flexible spending accounts. Eligible employees receive flexible vacation and sick leave, along with employer-paid life and disability insurance. The organization observes 11 federal holidays and an end-of-year winter break. Sabin also offers an employer-matching 401(k) plan.
Sabin is an Equal Opportunity Employer. All applicants will be considered for employment without attention to their race, color, religion, national origin, ancestry, age, disability or genetic information, sex (including gender identity, pregnancy or sexual orientation), marital status, veteran status, or any other characteristic protected by applicable federal, state or local laws.
Salary Description
$135,000 - $165,000

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