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Pharmaceutical Formulation Remote Jobs (NOW HIRING)

Remote, [#LI-Remote] in the state of Virginia. This role requires travel within the assigned ... Provide sales leadership in assigned geography through the formulation and execution of strategies ...

Remote, [#LI-Remote] in southern half of Florida. This role requires the candidate to live and ... Provide sales leadership in assigned geography through the formulation and execution of strategies ...

Remote, [#LI-Remote] in the state of Virginia. This role requires travel within the assigned ... Provide sales leadership in assigned geography through the formulation and execution of strategies ...

Remote, [#LI-Remote] in southern half of Florida. This role requires the candidate to live and ... Provide sales leadership in assigned geography through the formulation and execution of strategies ...

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Pharmaceutical Formulation Remote information

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$42

How much do pharmaceutical formulation remote jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for pharmaceutical formulation remote in the United States is $22.83, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $22.84 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Formulation Scientist in a remote role, and why are they important?

To thrive as a Pharmaceutical Formulation Scientist working remotely, you need a solid background in pharmaceutical sciences or chemistry, often supported by a relevant degree and industry experience in drug formulation. Familiarity with formulation software (such as Design of Experiments tools), data analysis programs, and regulatory documentation systems is typically required. Outstanding problem-solving, communication, and self-motivation skills set top candidates apart in a remote setting. These skills and qualifications are crucial for ensuring effective development, documentation, and cross-functional collaboration in pharmaceutical product creation, even when working off-site.

What is a Pharmaceutical Formulation Remote job?

A Pharmaceutical Formulation Remote job involves developing and optimizing drug formulations while working outside of a traditional laboratory or office setting, typically from home. Professionals in this role use scientific expertise to design, analyze, and improve the composition, stability, and delivery of pharmaceutical products. They often collaborate with cross-functional teams, document research findings, and ensure formulations meet regulatory requirements, all through digital communication and data analysis tools. This position is ideal for individuals seeking flexibility and who have experience in pharmaceutical sciences, chemistry, or related fields.

What are some typical challenges faced when working remotely in pharmaceutical formulation, and how can they be addressed?

One common challenge in remote pharmaceutical formulation roles is effective collaboration with laboratory and cross-functional teams, as much of the work depends on real-time data and physical sample evaluations. To address this, professionals often rely on robust digital communication tools, regular virtual meetings, and clear documentation to stay aligned with on-site colleagues. Maintaining organized records and proactively scheduling check-ins helps ensure timely feedback and project continuity. Additionally, remote workers should familiarize themselves with digital platforms for data sharing and project management to stay efficient and connected.

What is the difference between Pharmaceutical Formulation Remote vs Pharmaceutical Quality Control Remote?

AspectPharmaceutical Formulation RemotePharmaceutical Quality Control Remote
Primary FocusDeveloping and optimizing drug formulationsTesting and ensuring the quality of pharmaceutical products
Required SkillsFormulation science, lab techniques, regulatory knowledgeAnalytical testing, quality assurance, compliance standards
Work EnvironmentResearch labs, development teams, remote collaborationLaboratories, testing facilities, remote data analysis
Common CertificationsDegree in pharmacy, pharmaceutical sciences, or chemistryDegree in pharmacy, chemistry, or related field; certifications in quality assurance

Pharmaceutical Formulation Remote and Pharmaceutical Quality Control Remote roles both operate within the pharmaceutical industry but focus on different aspects. Formulation specialists develop new drug products, while quality control professionals ensure products meet safety and efficacy standards. Both roles often require similar educational backgrounds and can be performed remotely, but their daily tasks and objectives differ significantly.

More about Pharmaceutical Formulation Remote jobs
What cities are hiring for Pharmaceutical Formulation Remote jobs? Cities with the most Pharmaceutical Formulation Remote job openings:
What are the most commonly searched types of Pharmaceutical Formulation jobs? The most popular types of Pharmaceutical Formulation jobs are:
What states have the most Pharmaceutical Formulation Remote jobs? States with the most job openings for Pharmaceutical Formulation Remote jobs include:
Infographic showing various Pharmaceutical Formulation Remote job openings in the United States as of May 2026, with employment types broken down into 1% Locum Tenens, 50% Full Time, 48% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $47,488 per year, or $22.8 per hour.
Global Business Development Manager

Global Business Development Manager

ATS Automation Tooling Systems Inc

Warminster, PA • 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.
  •  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.  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.?  The three parallelograms in our logo reflect our core company values: People, Process, and Performance.  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.  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: 
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