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Telecommute Director Formulation Development Jobs

Research Scientist - Nutrition Formulation Department / Division: Nutrition Center of Excellence ... Amway is the leading direct selling company in the world, and its global Research and Development ...

Direct formulation development, testing, and optimization, including stability, package compatibility, PET, and safety assessments. * Ensure completion of required testing, including drug stability ...

Direct formulation development, testing, and optimization, including stability, package compatibility, PET, and safety assessments. * Ensure completion of required testing, including drug stability ...

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Telecommute Director Formulation Development information

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$89K

$191.4K

$287.5K

How much do telecommute director formulation development jobs pay per year?

As of Jun 4, 2026, the average yearly pay for telecommute director formulation development in the United States is $191,412.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,000.00 and $249,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Telecommute Director Formulation Development, and why are they important?

To thrive as a Telecommute Director Formulation Development, you need an advanced degree in pharmaceutical sciences or chemistry, extensive experience in drug formulation, and leadership in R&D. Proficiency with formulation software, regulatory submission platforms, and familiarity with GMP/GLP guidelines or certifications are typically required. Exceptional project management, communication, and cross-functional collaboration skills help drive virtual teams and align stakeholders. These competencies ensure effective formulation development, regulatory compliance, and successful product launches in a remote environment.

How does a Telecommute Director of Formulation Development typically collaborate with cross-functional teams while working remotely?

A Telecommute Director of Formulation Development leverages digital collaboration tools to coordinate with R&D, regulatory, manufacturing, and quality assurance teams. Regular virtual meetings, project management platforms, and shared documentation ensure seamless communication and progress tracking. Despite working remotely, directors are expected to proactively facilitate brainstorming sessions, resolve issues in real time, and maintain clear communication channels to drive project milestones. Building strong relationships and fostering team engagement are crucial to successfully overseeing formulation projects from early development to scale-up.

What does a Telecommute Director of Formulation Development do?

A Telecommute Director of Formulation Development oversees the design and improvement of pharmaceutical or chemical formulations while working remotely. This leadership role involves managing teams, coordinating cross-functional projects, ensuring regulatory compliance, and driving innovation in product development. They work closely with research, quality, and manufacturing departments to ensure products meet safety, efficacy, and quality standards, all while leveraging remote collaboration tools.

What is the difference between Telecommute Director Formulation Development vs Telecommute Formulation Scientist?

AspectTelecommute Director Formulation DevelopmentTelecommute Formulation Scientist
CredentialsAdvanced degree (PhD or MS), extensive industry experienceBachelor's or Master's degree in Chemistry, Pharmacy, or related field
Work EnvironmentLeadership role overseeing teams and projects remotelyHands-on research and formulation work, often collaborative but can be remote
Industry UsageUsed in pharmaceutical and biotech companies for strategic formulation leadershipCommonly employed in R&D labs for developing formulations

The main difference is that the Telecommute Director Formulation Development focuses on leading formulation teams and strategic planning remotely, while the Telecommute Formulation Scientist is involved in hands-on formulation research and development. The director role requires more experience and leadership skills, whereas the scientist role emphasizes technical expertise in formulation science.

More about Telecommute Director Formulation Development jobs
What cities are hiring for Telecommute Director Formulation Development jobs? Cities with the most Telecommute Director Formulation Development job openings:
What states have the most Telecommute Director Formulation Development jobs? States with the most job openings for Telecommute Director Formulation Development jobs include:
FSP Senior Scientist - Formulation Development, Biologics

FSP Senior Scientist - Formulation Development, Biologics

Thermo Fisher Scientific

New Brunswick, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 389 frontline employees who took The Breakroom Quiz

185th of 515 rated manufacturers


Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
Job Description
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.
Position Summary:
The candidate will support the Formulation team within Sterile Product & Device Development by executing formulation development and laboratory stability studies for parenteral drug products. This role is primarily lab based and focuses on high quality experimental execution, data generation, and support of formulation and characterization activities. The successful candidate is detail oriented, motivated by hands on work, and comfortable working in a collaborative team setting, with the ability to quickly learn and apply new laboratory techniques and automation platforms.
Key responsibilities:
• Support formulation development and stability studies through execution of laboratory experiments under guidance from senior team members.
• Prepare buffers, solutions, and samples for formulation, stability, and characterization studies using routine lab operations, including pipetting, liquid handling, aseptic techniques and filtration.
• Handle protein formulations using appropriate protein handling practices and aseptic techniques.
• Operate and support automated and semi automated laboratory systems; demonstrate willingness and ability to rapidly learn new automation tools.
• Maintain accurate and well organized experimental documentation in electronic laboratory notebooks and other electronic systems.
• Support general laboratory operations, including basic instrument care and compliance with safety and quality requirements.
• Participate in team discussions and contribute to a collaborative, accountable laboratory culture.
• The candidate will receive training on additional laboratory and analytical techniques, which may include but are not limited to: Particulate analysis; viscosity, density, and osmolality measurements; and basic HPLC analysis and routine instrument maintenance
Education and Experience:
• Bachelor's Degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or a related scientific discipline.
• 4- 6 years of hands on laboratory experience in formulation, analytical, or biophysical testing (academic or industry).
• Familiarity with protein handling and aseptic technique.
• Experience with fundamental laboratory techniques (pipetting, liquid handling, filtration, pH measurements, etc.) and buffer preparation.
• Comfort working in a laboratory environment with attention to detail, safety, and data integrity.
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Preferred Qualifications:
• Exposure to automated or high throughput laboratory systems.
• Experience supporting stability studies or regulated laboratory work.
• Familiarity with biopharmaceutical or sterile product development environments.
Competencies and Behavioral Expectations:
• Strong team player who collaborates effectively with colleagues.
• Highly organized with the ability to manage multiple tasks and priorities.
• Accountable and reliable in executing laboratory activities and meeting commitments.
• Personable, professional, and able to communicate effectively within a team setting.
Working Environment:
Below is listed the working environment/requirements for this role:
Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
Able to work upright and stationary and/or standing for typical working hours.
Able to lift and move objects up to 25 pounds
Able to work in non-traditional work environments.
Able to use and learn standard office equipment and technology with
proficiency.
May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
Benefits
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Compensation and Benefits
The salary range estimated for this position based in New Jersey is $70,000.00-$90,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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