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Remote Biologics Manufacturing Jobs (NOW HIRING)

Syner-G

Vice President, Biologics

Seattle, WA · Remote

This position is remote with significant travel to client sites, industry events, and business ... product manufacturing, and CMC regulatory strategy * Author and provide strategic input on CMC ...

Lonza

Director, Manufacturing

Walkersville, MD · On-site +1

$198K - $232K/yr

This position is currently remote. A future transition to an on-site location on the U.S. East ... biologics, or bioconjugate manufacturing environments * Demonstrated experience leading ...

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How much do remote biologics manufacturing jobs pay per hour?

As of Jul 27, 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:
What job categories do people searching Remote Biologics Manufacturing jobs look for? 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 July 2026, with employment types broken down into 94% Full Time, 3% Part Time, and 3% 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.
Engineer, Biologics Purification, Upstream/Downstream/Tech Transfer - Remote (JP15407)

Engineer, Biologics Purification, Upstream/Downstream/Tech Transfer - Remote (JP15407)

3 Key Consulting

Cambridge, MA • On-site, Remote

$34 - $37/hr

Full-time

Posted 6 days ago

Job description

Job Title: Engineer, Biologics Purification, Upstream/Downstream/Tech Transfer - Remote (JP15407)
Location: Cambridge MA, Remote
Employment Type: Contract
Business Unit: Drug Substance Technology Engineering Group
Duration: 1+ years with possible extensions and/or conversion to permanent
Posting Date: 5/21/2026
Pay Rate: $34 - $37/hour W2
Notes: Remote (Any TZ - Local to Cambridge, MA is highly preferred.
3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our client Cambridge site. Providing strong process engineering/ technology transfer support of human therapeutic drug substance products in clinical development through commercial production. Our mission is to translate developmental processes to commercial reality for patients through scientific expertise and engineering innovation. Knowledge of processes/equipment; scale-up factors, process deviations, quality attributes. GMP experience is a plus.
The Engineer will apply upstream and downstream process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in both stainless and single-use formats. Will partner with manufacturing, quality, analytical, and bench scientists to support a highly dynamic technology transfer.
JOB RESPONSIBILITIES:
Under guidance of senior staff, the Engineer will perform the following:
  • Transfer processes for drug substance manufacturing and translate process improvements from the laboratory into manufacturing facilities
  • Provide technical support for successful scale-up, transfer of process technology, and for clinical and/or commercial manufacturing operation. Experience is technical report writing an expectation.
  • Assist in troubleshooting clinical and commercial runs
  • Execute data trending and statistical process analysis
  • Support technical direction for process-related deviations, CAPAs, and change controls
  • Identify and support process-related operational excellence opportunities
  • Represent process development and collaborates with other functions such as Manufacturing, Quality, and Regulatory.
  • Experience related to Process characterization for manufacturing of biologics highly preferred. This includes technical support for authoring and review of process characterization reports.

Why is the Position Open?
Supplement additional workload on team.
BASIC QUALIFICATIONS:
Master’s degree and 2 years of Engineering or Operations experience
Bachelor’s degree and 4 years of Engineering or Operations experience
Associate’s degree and 7 years of Engineering or Operations experience
High school diploma / GED and 8 years of Engineering or Operations experience
PREFERRED QUALIFICATIONS:
  • Master’s Degree in Chemical or Biochemical Engineering
  • 2+ years of Process Engineering experience preferably related to downstream/ purification of commercial cGMP manufacturing facilities
  • Background in biologics technology transfer into commercial facilities, new product introductions (NPIs)
  • Biologics purification process knowledge: Knowledge of upstream ( cell culture/bioreactor operations) or purification processes (chromatography, viral filtration/inactivation, ultrafiltration/diafiltration, and final fill. )/ equipment; scale-up factors, process deviations, quality attributes
  • Strong analytical capability, troubleshooting, and problem solving
  • Independently motivated with ability to multi-task and work in teams, especially if remote or hybrid.
  • Excellent written and verbal communication skills with technical writing and presentation experience. Experience in PC documentation, report reviews and technical writing preferred.
     
Top Must Have Skills:
  • Cell culture experience, Purification /downstream experience, process characterization experience
  • Nice to have:
    Monoclonal antibodies or mAbs 
    manufacturing or on floor support 

Day to Day Responsibilities:
Assist senior staff in technical writing, process tech transfer, data monitoring
Red Flags:
No experience, not enough experience in biopharma or biotech, no experience in cell culture/upstream, purification/downstream or technical report writing
Interview process:
Teams interview. Screening 30 minute Microsoft team's interview with me. Second round- Team's interview 30 minute each approximately with 3 other team members.
We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.