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Remote Biologics Manufacturing Jobs (NOW HIRING)

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 ...

... Manufacturing and Control (CMC) and related pharmaceutical development activities of drug, biologic ... Opportunity for remote/hybrid* working depending on location * Leadership and mentoring ...

... Manufacturing and Control (CMC) and related pharmaceutical development activities of drug, biologic ... Opportunity for remote/hybrid* working depending on location * Leadership and mentoring ...

... Manufacturing and Control (CMC) and related pharmaceutical development activities of drug, biologic ... Opportunity for remote/hybrid* working depending on location * Leadership and mentoring ...

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Remote Biologics Manufacturing information

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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.
Business Development Manager, Biologics (East Coast Based)

Business Development Manager, Biologics (East Coast Based)

The U.S. Pharmacopeial Convention (USP)

Tallahassee, FL • Remote

Full-time

Medical, Retirement, PTO

Posted 9 days ago


Job description

Who is USP?

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide.

At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.

USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.

How will YOU create impact here at USP?

The Business Development Manager, Biologics position is leading the execution of the commercial strategy for USP portfolio of standards and materials for Biopharmaceutical industry in United States. This is an important, non-supervisory role responsible for driving revenues growth, expanding market presence, and accelerating USP’s impact across the biopharmaceutical industry in United States.

In this role, you will be accountable for meeting revenues and units’ growth annual targets in your assigned territory (United States). To achieve this, you will foster customer relationships at all levels and collaborate with multiple internal USP functions including Technical and Customer Service, Marketing, Regulatory and Scientific Affairs to deliver unmatched customer experiences.

Your activities will include regular account management and business development customer visits, business leads follow up, lead generation activities as well as distribution channels management.

You will lead creation and execution of accounts plans to position USP portfolio of standards for long term growth. Your focus will be on identifying, understanding and supporting resolution of key quality challenges that developers and manufacturers of biologics drugs are routinely facing. You will also oversee the positioning USP in new high growth therapeutic fields (cell and gene therapies, nucleic acid drugs, monoclonal antibodies, etc.) and markets.

The successful candidate will be self-motivated, and results driven. They will enjoy working with people collaboratively, strengthening customer relationships, and developing their network in the biopharmaceutical community.

We are searching for a person who wants to grow and develop their own career, a future commercial leader with a passion for opening new doors and creating new opportunities. This is a remote position residing in one of the following states: New Hampshire, Maryland, DC, Virginia, Pennsylvania, North Carolina, or Florida, requiring up to 60% domestic travel.

As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.

Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.

This hire MUST reside in New Hampshire, Maryland, DC, Virginia, West Virginia, Pennsylvania, North Carolina, or Florida due to travel and client interaction purposes. USP will consider relocation assistance for those who wish to relocate from another area.

The Business Development Manager – Biologics, has the following responsibilities:

Revenue Growth:

  • Achieve revenues and units’ growth target for their territory and accounts.
  • Develop and execute plans to protect and grow revenues at existing accounts and drive new customers’ acquisition. Manage sales activities in Salesforce CRM.
  • Collaborate with business support functions (Marketing, Inside Sales, Science team, etc.) and support the execution of revenues growth initiatives in their territory.
  • Identify and influence key decision makers in the buying process toward USP products and services.
  • Responsible for following up on sales qualified leads.
  • Build strong, collaborative partnerships with USP distributors, ensuring proper training of distributor sales reps, access to sales collaterals and executing joint customer visits as needed.
  • Identify and unlock opportunities in emerging therapeutic areas and high-growth markets such as cell & gene therapies, nucleic acid drugs, and monoclonal antibodies, to position USP as a leader in biologics standards.

Customer Engagement:

  • Cultivate and strengthen customer relationships at all levels, positioning USP as a trusted advisor to biopharmaceutical developers and manufacturers.
  • Partner with customers to understand and help address critical quality challenges in biologics development and manufacturing.
  • Partner with Scientific Affairs, BIO Science and Marketing teams to deliver seamless and differentiated customer experiences through organization of customer events.
  • Attend industry trade shows, conferences, and professional forums as appropriate, elevating the organization’s visibility and influence.

Data-Driven Insights & Sales Intelligence:

  • Use of Salesforce CRM and data analytics to track sales performances and inform your actions.
  • Analyze and interpret your territory sales data—direct and through distributors—to identify revenue opportunities and provide strategic business reviews.
  • Gather and consolidate market and customer feedback, providing actionable recommendations to Global Marketing and Strategy teams as appropriate.

Who is USP Looking For?

The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:

  • Bachelor's degree in a life sciences discipline (preferably analytical chemistry, biochemistry, biology, microbiology, biotechnology) with a minimum of 5-years professional experience in life sciences industry.
  • At least 3 years of experience as an account manager in life sciences industry, with a track record of consistently meeting sales targets.
  • Proven experience in selling products or services to pharma and biopharma accounts (PD labs and QC labs target functions).
  • Familiarity with bioproduction (mAbs, vaccines, CGT’s) and clinical development process.
  • Strong problem-solving skills with customer-centric approach.
  • Bias to action and results driven with a track record of successful outcomes.
  • Excellent interpersonal skills, presentation, communications skills.
  • Excellent relationship-building skills with customers.
  • Strong time management, multi-tasking, and organizational skills.
  • Accountability and ownership of work.
  • Strong verbal and written communication skills.
  • Self-motivated and able to work in a fast-paced multi-task environment.
  • Proficiency with Microsoft Office, data analytical platform (e.g. Tableau) and CRM (e.g. Sales Force).
  • Ability and desire to work well with diverse employees and customers in a cooperative and friendly manner.

Additional Desired Preferences

  • Master’s degree preferred in either business or science with an MBA. Education and training in pharmaceutical sciences and business are highly desired. 
  • Ability to gain customer confidence and build long-term relationships.
  • Ability to listen and gather customer/stakeholder insights and respond with creative solutions.
  • Team player who is self-motivated with strong interpersonal skills and works well in a collaborative entrepreneurial environment.
  • Strong project management and communication skills.
  • Experience with regulatory, quality assurance or GMP background.
  • Existing relationships with decision makers in the pharma/biopharma markets preferred, including manufacturers, trade associations and/or retailers.

Supervisory Responsibilities

None, this is an individual contributor role.

Benefits

USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.

Compensation

Base Salary Range: USD $98,900 – $127,250 annually.

Target Annual Bonus: 13% target.

Individual compensation packages are based on various factors unique to each candidate’s skill set, experience, qualifications, equity, and other job-related reasons.

 

 Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.