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Remote Biologics Manufacturing Jobs (NOW HIRING)

Senior Scientist - Biologics

Petersburg, VA · On-site +1

$89K - $122K/yr

Our Biologics Development team brings essential biosimilar medicines to our patients in the United ... remote work style with travel to Civica's Petersburg, Virginia manufacturing facility and Lehi ...

CMO Director, US

Durham, NC · Remote

$200K - $260K/yr

Remote - East Coast Preferred (EST) Department: External Manufacturing Reports To: Head of External ... Experience in vaccines, sterile manufacturing, or biological drug product operations * Familiarity ...

Whether you're scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting ... This role is remote-eligible and requires approximately 30% travel to Forge Biologics' headquarters ...

Whether you're scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting ... This role is remote-eligible and requires approximately 30% travel to Forge Biologics' headquarters ...

Whether you're scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting ... This role is remote-eligible and requires approximately 30% travel to Forge Biologics' headquarters ...

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Remote Biologics Manufacturing information

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$13

$24

$34

How much do remote biologics manufacturing jobs pay per hour?

As of Jun 9, 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 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 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 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.

More about Remote Biologics Manufacturing jobs
What cities are hiring for Remote Biologics Manufacturing jobs? Cities with the most Remote Biologics Manufacturing job openings:
What are the most commonly searched types of Biologics Manufacturing jobs? The most popular types of Biologics Manufacturing jobs are:
What states have the most Remote Biologics Manufacturing jobs? States with the most job openings for Remote Biologics Manufacturing jobs include:
Infographic showing various Remote Biologics Manufacturing job openings in the United States as of June 2026, with employment types broken down into 89% Full Time, and 11% Part Time. Highlights an 100% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.
Manager, Quality Assurance, External Manufacturing

Manager, Quality Assurance, External Manufacturing

Vaxcyte

San Carlos, CA • On-site, Remote

$151K - $176K/yr

Other

Posted 10 days ago


Job description

Summary:

The Manager, Quality Assurance, External Manufacturing is responsible for overseeing quality activities at contract manufacturing organizations (CMOs), ensuring compliance with cGMP standards, and driving performance through KPIs and continuous improvement initiatives. This role leads batch disposition, reviews critical GMP documentation, supports PPQ activities, and collaborates cross-functionally to resolve complex manufacturing and quality issues. The position requires strong expertise in pharmaceutical quality systems, regulatory requirements, and risk management, along with leadership, problem-solving, and communication skills to support both clinical and commercial operations.

Essential Functions:
  • Provide Quality Assurance oversight of Contract Manufacturing Organizations (CMOs).
  • Develop and report metrics and key performance indicators (KPIs) to evaluate CMO performance.
  • Represent Quality Assurance at internal cross-functional meetings and Joint Project Team meetings.
  • Lead polysaccharide batch disposition activities, including review of executed batch records, environmental monitoring data, and quality control results.
  • Review and approve GMP documentation, including master batch records, deviations, risk assessments, change controls, and CAPAs.
  • Drive resolution of quality performance issues in collaboration with contract manufacturers.
  • Support Process Performance Qualification (PPQ) activities.
  • Develop, implement, and maintain quality procedures, policies, and standards.
  • Collaborate with key stakeholders to develop solutions to complex manufacturing and quality issues.
  • Participate in compliance audits and regulatory inspections, as required.
  • Promote a strong quality mindset and a culture of quality excellence across all activities.
Requirements: 
  • Bachelor's degree in chemistry, Biology, Pharmacy, Engineering, or a related scientific discipline.
  • Minimum 5 years of experience in managing CMO quality, and quality systems management within the pharmaceutical, biotechnology, or life sciences industry. Other combinations of education and experience may be considered.
  • Experience in batch record review, deviations and Out of Specification (OOS) investigations.
  • Thorough knowledge of cGMP, ICH guidelines, FDA/EMA, Swiss medic regulations, and international pharmaceutical quality standards.
  • Experience applying Quality Risk Management principles.
  • Experience supporting both clinical and commercial products preferred.
  • Strong leadership, management, and process improvement skills.
  • Excellent organizational skills with strong attention to detail.
  • In-depth understanding of biologics manufacturing operations.
  • Proven ability to prioritize multiple assignments in a fast-paced, changing environment.
  • Strong problem-solving abilities, including managing complex investigations and root cause analyses.
  • Excellent written and verbal communication skills, with the ability to clearly present quality topics and risk-based decisions to cross-functional teams.
Reports to: Director, Quality Assurance
 
Location: Open to Remote; San Carlos, CA
 
Compensation:
The compensation package will be competitive and includes comprehensive benefits and an equity component.
 
Salary Range: $151,000 - $176,000 (SF Bay Area). Salary ranges for non-California locations may vary.

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About Vaxcyte

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

51 - 200 Employees

Headquarters location

San Carlos, CA, US

Year founded

2013