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Remote Sterile Manufacturing Jobs (NOW HIRING)

... manufacturing. ABEC's unique value is based on combining long experience with the ability to ... sterilization systems. THIS IS A REMOTE ROLE - Ideal candidates will reside within North Carolina ...

... manufacturing. ABEC's unique value is based on combining long experience with the ability to ... sterilization systems. THIS IS A REMOTE ROLE -- Ideal candidates will reside within North Carolina ...

... sterile liquid pharmaceutical manufacturing and packaging equipment and systems. The role will ... This position does not offer remote or hybrid work options, and candidates must be willing to ...

... sterile liquid pharmaceutical manufacturing and packaging equipment and systems. The role will ... This position does not offer remote or hybrid work options, and candidates must be willing to ...

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Field Service Engineer

Springfield, NJ ยท Remote

$80K - $100K/yr

Pharmaceutical Packaging * Pharmaceutical or Biotech Manufacturing Equipment * Strong ... Experience with sterile injectable or aseptic processing equipment. * Experience supporting ...

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Field Service Engineer

Springfield, NJ ยท Remote

$80K - $100K/yr

Pharmaceutical Packaging * Pharmaceutical or Biotech Manufacturing Equipment * Strong ... Experience with sterile injectable or aseptic processing equipment. * Experience supporting ...

This is a Remote position with the preferred location being Bozeman, MT or Denver, CO. Other USA ... Our Sterilization and Disinfection Control division manufactures and sells biological and chemical ...

... Remote RSO Support services using best practices. The role is responsible for managing and ... Our forward-looking companies lead the way in healthcare sterilization, industrial safety ...

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Remote Sterile Manufacturing information

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How much do remote sterile manufacturing jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for remote sterile manufacturing in the United States is $27.49, according to ZipRecruiter salary data. Most workers in this role earn between $19.95 and $33.17 per hour, depending on experience, location, and employer.

What are some common challenges faced in a remote sterile manufacturing role, and how can they be addressed?

In a remote sterile manufacturing role, one common challenge is maintaining strict adherence to sterility protocols while coordinating with team members who may be working from different locations. Effective digital communication tools and clear documentation are essential for ensuring all procedures are properly followed and tracked. Additionally, troubleshooting equipment or process issues remotely can be difficult, so proactive maintenance schedules and thorough remote training sessions help mitigate risks. Team collaboration often relies on regular virtual meetings and shared platforms to monitor batch progress, quality control, and compliance updates.

What is remote sterile manufacturing?

Remote sterile manufacturing refers to the production of sterile pharmaceutical or medical products in facilities where many operations are monitored, managed, or controlled remotely, often using digital systems and automation. This approach allows for enhanced quality control, improved efficiency, and reduced risk of contamination, as human interaction is minimized. Remote sterile manufacturing is essential in ensuring that products such as injectables, vaccines, and other sterile medicines meet strict regulatory standards for safety and cleanliness.

What is the difference between Remote Sterile Manufacturing vs Remote Quality Assurance in the pharmaceutical industry?

AspectRemote Sterile ManufacturingRemote Quality Assurance
CredentialsCertifications in sterile processing, GMP trainingCertifications in quality management, GMP, and validation
Work EnvironmentManufacturing facilities, cleanrooms, labs (remote oversight possible)Office or remote settings reviewing processes, audits, documentation
Industry UsageProduction of sterile pharmaceuticals, vaccinesEnsuring product quality, compliance, and validation

Remote Sterile Manufacturing involves overseeing the production of sterile products, often requiring GMP compliance and sterile processing certifications. Remote Quality Assurance focuses on reviewing quality systems, audits, and documentation to ensure compliance. Both roles are essential in pharmaceutical manufacturing, with overlapping credentials but different daily responsibilities, making them common comparison points for job seekers.

What are the key skills and qualifications needed to thrive in Remote Sterile Manufacturing, and why are they important?

To succeed in Remote Sterile Manufacturing, you need a solid understanding of aseptic techniques, GMP (Good Manufacturing Practices), and a relevant scientific or technical background. Familiarity with automated manufacturing systems, environmental monitoring tools, and compliance certification such as GxP or ISO standards is typically required. Attention to detail, problem-solving skills, and effective communication are crucial soft skills for maintaining product quality and ensuring process integrity. These competencies are essential to consistently produce safe, sterile products and meet strict regulatory requirements in a remote or distributed work environment.
More about Remote Sterile Manufacturing jobs
What cities are hiring for Remote Sterile Manufacturing jobs? Cities with the most Remote Sterile Manufacturing job openings:
What are the most commonly searched types of Sterile Manufacturing jobs? The most popular types of Sterile Manufacturing jobs are:
What states have the most Remote Sterile Manufacturing jobs? States with the most job openings for Remote Sterile Manufacturing jobs include:
Infographic showing various Remote Sterile Manufacturing job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 85% Full Time, 9% Part Time, 3% Contract, and 2% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $57,186 per year, or $27.5 per hour.
Global Business Development Manager

Global Business Development Manager

ATS Automation Tooling Systems Inc

Warminster, PA โ€ข Remote

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago


Job description

SP Industries Inc., an ATS Company is seeking an experienced Global Business Development Manager to lead worldwide sales and market expansion for our aseptic and non-aseptic lyophilization equipment portfolio. This is a player coach role, combining direct responsibility for driving new business with leadership of a team of lyophilization sales and subject matter experts. The position focuses on selling high value pharmaceutical lyophilization systems to customers across the biopharma, biotech, diagnostics, and related life science markets.

The role is accountable for driving large, complex capital equipment deals within the aseptic lyophilization space, leading and managing commercial efforts, executing strategy, and building a robust, sustainable global pipeline. The ideal candidate brings a strong background in aseptic processing and a proven track record of developing global pipelines and closing major, high value transactions, along with the leadership capability to grow into a broader management role over time. This position is remote based in North America and requires international travel to develop opportunities and support regional teams.

Key Responsibilities

  • Own and drive global revenue growth across the aseptic and non aseptic lyophilization portfolio, with direct accountability for closing large, complex, high value pharmaceutical and biopharma capital equipment and system solutions.
  • Define and execute the global commercial strategy for lyophilization systems, leveraging strong understanding of lyophilization cycle development, formulation considerations, CIP/SIP systems, and sterility assurance requirements to deliver differentiated, value based solutions.
  • Serve as a senior commercial and technical authority across non-aseptic and aseptic filling and lyophilization, with strong working knowledge of EU GMP Annex 1, FDA expectations, cleanroom classifications, isolators/RABS, aseptic process simulations, validation strategies, and quality risk management.
  • Lead the sale of fully integrated system solutions, including lyophilization, automated loading and unloading, material handling, controls, and supporting architectures-positioning SP as a total solution partner rather than a standalone equipment supplier.
  • Apply practical knowledge of GAMP 5, computerized systems, and validation expectations to support compliant system design discussions, risk mitigation, and customer confidence throughout the sales process.
  • Build, qualify, and actively manage a robust global pipeline, including ownership of forecasting, financial modeling, and business case development to support accurate revenue planning and strategic investment decisions.
  • Personally engage senior customer stakeholders across engineering, manufacturing, quality, procurement, and executive leadership to influence complex buying decisions, support contract negotiations, and close strategic, multi site opportunities.
  • Lead and develop a team of lyophilization commercial based subject matter experts, setting clear commercial priorities, driving accountability, and ensuring technical depth directly supports deal execution and customer success.
  • Partner cross functionally with engineering, product management, project management, manufacturing, and service teams to shape commercially viable offerings, influence service strategies, and ensure end to end solutions meet customer, regulatory, and operational requirements.
Additional Responsibilities
  • Maintain a strong understanding of biologics, vaccines, small molecule injectables, and sterile drug products, along with global outsourcing drivers, capacity constraints, and competitor capabilities impacting the lyophilization and aseptic processing market.
  • Continuously assess competitive landscape positioning and identify evolving market needs (e.g., high potency products, biologics, accelerated development timelines), proactively adjusting commercial strategy to sustain competitive advantage. Apply practical knowledge of GAMP 5, computerized systems, and validation expectations to support compliant system design discussions, risk mitigation, and customer confidence throughout the sales process.
  • Build, qualify, and actively manage a robust global pipeline, including ownership of forecasting, financial modeling, and business case development to support accurate revenue planning and strategic investment decisions.
  • Personally engage senior customer stakeholders across engineering, manufacturing, quality, procurement, and executive leadership to influence complex buying decisions, support contract negotiations, and close strategic, multi-site opportunities.
  • Lead and develop a team of lyophilization commercial based subject matter experts, setting clear commercial priorities, driving accountability, and ensuring technical depth directly supports deal execution and customer success.
  • Partner cross functionally with engineering, product management, project management, manufacturing, and service teams to shape commercially viable offerings, influence service strategies, and ensure end to end solutions meet customer, regulatory, and operational requirements.
  • Maintain a strong understanding of biologics, vaccines, small molecule injectables, and sterile drug products, along with global outsourcing drivers, capacity constraints, and competitor capabilities impacting the lyophilization and aseptic processing market.
  • Continuously assess competitive landscape positioning and identify evolving market needs (e.g., high potency products, biologics, accelerated development timelines), proactively adjusting commercial strategy to sustain competitive advantage.
  • Support and enable regional sales teams globally by providing deal strategy leadership, technical guidance, and direct customer engagement to accelerate opportunity progression and conversion.
  • Represent the organization at key industry forums, customer workshops, and strategic engagements, reinforcing SP's credibility as a global leader in lyophilization system solutions.
Experience / Qualifications:
  • 7+ years of experience in pharmaceutical, biopharma, or life science capital equipment or system solutions, with a strong focus on aseptic processing and/or lyophilization.
  • Proven track record of closing large, complex, multi million dollar pharmaceutical system deals with biopharma, biotech, diagnostics, or CDMO customers.
  • Demonstrated ability to build and convert a global sales pipeline, including direct ownership of opportunity creation, deal progression, and bookings
  • Working knowledge of EU GMP Annex 1 and its impact on aseptic lyophilization system design, automation, contamination control, and customer requirements.
  • ย Practical understanding of GAMP 5 principles, including computerized systems, controls, data integrity, and validation expectations in regulated environments.
  • Experience selling or supporting fully integrated aseptic system solutions, including lyophilizers, automated loading/unloading, material handling, and associated system architectures.
  • Ability to engage credibly with senior customer stakeholders across engineering, manufacturing, quality, and executive leadership.
  • Experience operating in a player coach capacity, combining direct commercial responsibility with leadership of technical SMEs or solution specialists.
  • Bachelor's degree in engineering, life sciences, or a related technical discipline.
  • Willingness to travel globally 30-50%.
Physical Demands

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • The employee is regularly required to talk and listen.
  • The employee is regularly required to use color vision and work with computerized data.
  • The employee is regularly required to stand, walk, and sit.
  • The employee is occasionally required to lift up to 20 pounds.
  • The employee is regularly required to use normal office tools, equipment and PC's.
HSE:

All managers are responsible for creating a positive safety culture and maintaining a saf
and healthy workplace. It is the responsibility of each manager to ensure that employees.
receive regular training regarding health, safety and environmental matters. ย Each
manager is also accountable to ensure that HSE matters are addressed in a timely manner.
and that compliance with both legislative and corporate requirements are maintained.

Manager responsibilities for Health, Safety and Environment include:

  • Demonstrate leadership in Health, Safety and Environment compliance
  • Hold team members accountable for health, safety and environmental compliance as part of the annual performance review process
  • Ensure that the requirements of the health, safety and environment management system are implemented and maintained
  • Carry out hazard assessments, inspections, and audits as required by legislative framework and/or corporate requirements
  • Ensure that training is provided to all departmental employees are per established training matrix
  • Implement appropriate corrective measures for unsafe conditions and unsafe acts
  • Ensure that appropriate equipment, materials and protective devices are provided and maintained in safe condition
  • Provide information, instruction and supervision to employees
  • Take every precaution reasonable in the circumstances for the protection of employees

Why SP Industries Inc.? ย The three parallelograms in our logo reflect our core company values: People, Process, and Performance. ย As part of ATS, Scientific Products leverages the ATS Business Model (ABM) to train, develop, engage, empower, and energize our people to make impactful changes in the organization. ย Our relentless focus on people is what continues to set us apart as a great place to build a career.
We provide a wide range of innovative and high-quality scientific products that improve people's lives
We offer a robust health and welfare benefits package that includes Life, Health, Dental, Vision
We offer 401(K) including company match, Paid Time Off annually + Paid Holidays
You will enjoy career Advancement Opportunities and Tuition Assistance to help you achieve your goals and continue your career growth

EEO and Affirmative Action Statement:
SP is an Equal Opportunity Employer, dedicated to a policy of non-discrimination in employment on any basis and takes affirmative action to ensure equal employment opportunities. It is our policy to provide our employees and applicants with equal employment opportunities in accordance with applicable laws and not to discriminate on the basis of race, color, religion, ancestry, national origin, age, marital status, sex, gender identification, sexual orientation, genetic information, political belief, pregnancy, citizenship, handicap or disability, status as a veteran or member of the U.S. military, or any other characteristic protected by applicable federal, state, or local laws. SP's Affirmative Action Plan is available through the HR Department and may be accessed during normal business hours.


Pay Transparency Nondiscrimination Provision:ย 
SP will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. #LI-Remote