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Telecommute Director Formulation Development Jobs

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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:
Director, Formulation and Process Development

Director, Formulation and Process Development

Astrazeneca

New Haven, CT

$175K - $263K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago


AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 71 rated pharmaceutical


Job description

You will lead and direct the formulation and process development of patient-centered injectable drug products.These products are for Alexion's diverse portfolio, which spans synthetic, peptide, genomic medicine, and protein-based modalities in multiple formats, including liquid, lyophilized, vial, prefilled, and cartridge-based presentations. You will also lead life cycle development opportunities, provideexpertisein technology transfer and drug product engineering and technology development with internal and external partnerships. You will also ensure the development of portfolio projects in a phase-appropriate manner while managing the budget and interface partners. You will be a member of the Injectable Drug Product Management team and will need to collaborate and network with other departments within Product Development and Clinical Supplies (PDCS). Additionally, it will need to collaborate and network with Alexion Operations, Clinical Development, Quality, and Regulatory organizations.

You Will:

  • Formulation and process development and manufacturing of patient-centered, unique injectable drug products for Alexion's diverse portfolio from pre-clinical to successful licensure.

  • Develop drug productdevelopmentstrategies through internal/external partnerships and product integration into drug/device combination products.

  • Enablethe progression of Alexion'sdiverse portfoliothatspans peptide, nucleic acid, protein-based modalities, as well as modalities for gene deliveryasliquid and lyophilized dosage forms in vial, prefilled syringe, and cartridge-based presentations.

  • Ensure tech transfer of Alexion's portfolio with specialized input on engineering solutions for equipment and processes.

  • Review and develop drug producttechnologyroadmap and manage important investments.

  • Mentorand developcolleagues in a matrix team for efficient and successful drug product development and manufacturing in a phaseappropriate manner.

  • Partner with functions across Alexion to build the best strategies for developing products in Alexion's diverse portfolio.

  • Provide subject matterexpertisefor preparing regulatory filings, regulatory interactions including inspections, audits and is accountable for the technical content of the relevant drug product sections of regulatory submissions.

  • Work with the Head on the developmentondrug product development strategies within PDCS and with partners in Operations, Regulatory Affairs, and Commercial organizations.

You Have:

  • Must have a BS or equivalent in Bio/Chemical Engineering, Pharmaceutical Sciences, Biochemistry, or related discipline with relevant experience

  • At least 8 years of experience in managing a group of drug product development scientists or engineers withendtoenddrug product developmentexperience(spanning formulation, process development, quality attribute assessment,techtransferand manufacturing support)formAbs,fusionproteins,injectablepeptides/syntheticsprograms.

  • At least 5 years of experience managing a team of scientists and engineers atdifferent levels(directly or in a matrix team)and ensuring their career growth.

  • Must be proficient in current approaches for formulation and drug product process development, manufacturing processes and equipment,regulatory expectationsand applying these to developing efficient approaches to ensure product licensure.

  • Knowledge of high concentration protein formulation development, aseptic processes, vial, prefilled syringe, cartridge presentations,liquid and lyophilization dosage forms is important.

  • Knowledge of current regulatory guidelines and cGMP requirements is necessary

Benefits offered include:

  • A qualified retirement program [401(k) plan]

  • Paid vacation, holidays, and paid leaves

  • Health benefits including medical, prescription drug, dental, and vision coverage following the terms and conditions of the applicable plans.

Additionaldetails of participation in these benefit plans will be provided if an employee receives an offer of employment.The annual base salary for this position ranges from $175,000 to $263,000. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility toparticipatein our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).

#LI-Onsite #Alexion

Date Posted

29-May-2026

Closing Date

29-Jun-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.


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