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Telecommute Director Formulation Development Jobs in Azusa, CA

Head of R&D

Los Angeles, CA · On-site

$190K - $210K/yr

Dr. Squatch is seeking a Head of R&D to lead the next phase of technical and product innovation ... The ideal candidate combines deep formulation expertise with strong operational judgment and an ...

Senior Food Scientist

Los Angeles, CA · On-site

$95K - $120K/yr

Director of R&D Marketing Message Are you passionate about bringing innovative food products from ... Conduct bench-top formulation work, ingredient evaluations, sensory testing, and prototype ...

Head of R&D

Los Angeles, CA · On-site

$190K - $210K/yr

The ideal candidate combines deep formulation expertise with strong operational judgment and an ... Agencies are hereby specifically directed NOT to contact DRSQ employees directly in an attempt to ...

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Telecommute Director Formulation Development information

See Azusa, CA salary details

$90.5K

$194.7K

$292.5K

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

As of Aug 24, 2026, the average yearly pay for telecommute director formulation development in Azusa, CA is $194,730.00, according to ZipRecruiter salary data. Most workers in this role earn between $95,600.00 and $253,300.00 per year, depending on experience, location, and employer.

What does a telecommute director 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 are the key skills and qualifications needed to thrive as a telecommute director formulation development?

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 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 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.

What cities near Azusa, CA are hiring for Telecommute Director Formulation Development jobs?

Cities near Azusa, CA with the most Telecommute Director Formulation Development job openings:

Infographic showing various Telecommute Director Formulation Development job openings in Azusa, CA as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $194,730 per year, or $93.6 per hour.

Senior Formulation Scientist, Sterile & Peptide Product Development

Socket.dev

Los Alamitos, CA • On-site

$150 - $210/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago


Job description

Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we’re making better health outcomes easier to achieve.

Hims & Hers is a public company, traded on the NYSE under the ticker symbol “HIMS.” To learn more about the brand and offerings, you can visit hims.com/about and hims.com/how-it-works . For information on the company’s outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit www.hims.com/careers-professionals.

About the Role:

We're looking for a Senior Formulation Scientist to join our Sterile Product Development (SPD) team, supporting the development and optimization of both sterile injectable products and peptide-based therapeutics. In this role, you'll lead formulation strategy and process development across a diverse product portfolio, supporting programs from early feasibility through commercial scale-up and lifecycle management.

You'll bring deep technical expertise in sterile injectable and peptide formulation development, working cross-functionally with Manufacturing Sciences & Technology (MS&T), Quality, and Regulatory teams to design robust, scalable formulations that meet CGMP and FDA 503B requirements. This is a senior technical role with room to shape formulation strategy, mentor junior scientists, and help expand our sterile and peptide portfolio.

You Will:
  • Lead formulation and process development for sterile injectable and peptide‑based products, including solutions, suspensions, and long‑acting injectable formats.
  • Design and execute pre‑formulation, excipient compatibility, and forced‑degradation studies specific to peptide stability, including oxidation, deamidation, aggregation, and hydrolysis pathways.
  • Develop and optimize stability programs aligned with ICH Q1A(R2) and Q5C, including BUD (beyond‑use date) justification for compounded and sterile products.
  • Provide technical input into peptide API selection, characterization, and make‑vs‑buy evaluations in partnership with cross‑functional stakeholders.
  • Design lab‑and pilot‑scale studies to assess formulation feasibility, freeze‑thaw stability, container‑closure compatibility, and process robustness.
  • Author and review technical reports, stability protocols, and formulation development summaries to support regulatory filings and internal decision‑making.
  • Partner with MS&T, Quality, and Operations to ensure smooth technology transfer of sterile and peptide formulations from lab to commercial manufacturing across sites.
  • Support OOS/OOT investigations and CAPA implementation related to sterile and peptide product stability and quality.
  • Provide scientific mentorship to formulation scientists and technicians, and contribute to SOP development and gap analyses (e.g., ICH stability guideline alignment).
  • Stay current on peptide delivery technologies, degradation science, and analytical methods, and evaluate new technologies for lifecycle management.
You Have:
  • Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field with 6–8+ years of industry experience, or B.S./M.S. with 8–10+ years of experience in sterile injectable product development, including direct peptide formulation work.
  • Hands‑on experience formulating peptide therapeutics for parenteral administration (solutions, suspensions, or lyophilized products).
  • Demonstrated experience developing sterile injectable (parenteral) drug products, with direct involvement in formulation design, fill/finish considerations, and container‑closure selection.
  • Strong understanding of peptide‑specific degradation pathways and stability‑indicating analytical methods.
  • Experience designing and executing stability studies in accordance with ICH Q1A(R2)/Q5C and USP/FDA 503B requirements.
  • Proficiency in analytical data interpretation (UPLC/HPLC, mass spectrometry, impurity profiling, and related peptide characterization methods).
  • Experience with formulation scale‑up and technology transfer within CGMP environments.
  • Excellent technical writing, documentation, and cross‑functional communication skills.
Preferred
  • Experience evaluating third‑party API/BUD data packages and providing technical recommendations as part of make‑vs‑buy sourcing decisions.
  • Familiarity with long‑acting injectable or novel peptide delivery technologies.
  • Experience with regulatory documentation and submissions (IND/NDA or 503B filings).
  • Prior leadership or mentorship experience within a formulation or analytical team.
  • Experience managing multi‑site technology transfer (e.g., coordinating between development and manufacturing facilities).
Our Benefits (there are more but here are some highlights):
  • Competitive salary & equity compensation for full‑time roles
  • Unlimited PTO, company holidays, and quarterly mental health days
  • Comprehensive health benefits including medical, dental & vision, and parental leave
  • Employee Stock Purchase Program (ESPP)
  • 401k benefits with employer matching contribution
  • Offsite team retreats

We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging.

Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Hims & Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at accommodations@forhims.com and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims & Hers gives consideration to all qualified applicants without regard to any protected status, including disability. Please do not send resumes to this email address.

To learn more about how we collect, use, retain, and disclose Personal Information, please visit ourGlobal Candidate Privacy Statement.

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