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Remote Pharmaceutical Formulation Development Jobs

Atomic

CMC Consultant

... pharmaceutical settings. * Expertise in formulation development, analytical method development/validation, stability programs, GMP manufacturing, and quality compliance. * Strong knowledge of FDA ...

Debut Biotech

Director, Formulation Sales

San Diego, CA · On-site +1

$150K - $180K/yr

San Diego-based preferred but remote may be considered for the right candidate. This role sits ... Build and maintain strong relationships with key decision makers across R&D, product development ...

A-Line Staffing Solutions

Be Seen First

Remote - Pharmacist Advisor - Medicare

Phoenix, AZ · Remote

$53/hr

Pay: From $53.00 per hour Clinical Pharmacist Advisor - Medicare Part D Appeals Fully Remote ... Participate in coaching, development discussions, and feedback sessions with the direct supervisor

Codera

Director, CMC - Formulations

San Diego, CA · Remote

$190K - $260K/yr

... develop and commercialize pharmaceutical products. Position Summary The Director, CMC ... formulation topics to support Tang Capital's investments * Participate in business development ...

Hims and Hers Health, Inc.

Manager, Material Scientist

$140K - $160K/yr

This is a remote role with occasional travel. You Will: * Lead physicochemical characterization of ... Troubleshoot formulation and material-related issues across both development and commercial ...

BridgeBio Pharma

Director, Analytical Development

$144K - $159K/yr

Where You'll Work Remote with 30% travel anticipated Who You Are MS in Organic Chemistry ... pharmaceutical/biotech industry. Demonstrated abilities in the development and application of ...

PharmD Live

Pharmacist (Hawaii - Remote)

HI · Remote

$62.50 - $75.25/hr

Pharmacist (Hawaii - Remote) Work Arrangement: Fully Remote Target Location: Hawaii (HI) Licensure ... Professional development support

PharmD Live

Pharmacist (Hawaii - Remote)

$59.50 - $71.75/hr

Pharmacist (Hawaii - Remote) Work Arrangement: Fully Remote Target Location: Hawaii (HI) Licensure ... Professional development support

Hometown Pharmacy

Remote Managing Pharmacist

$59.50 - $71.75/hr

... and development. * Support consistent implementation of pharmacy policies and procedures ... Professional Expectations The Remote Managing Pharmacist is expected to: * Maintain the highest ...

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Remote Pharmaceutical Formulation Development information

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How much do remote pharmaceutical formulation development jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for remote pharmaceutical formulation development in the United States is $50.89, according to ZipRecruiter salary data. Most workers in this role earn between $34.62 and $81.49 per hour, depending on experience, location, and employer.

What is remote pharmaceutical formulation development?

Remote pharmaceutical formulation development refers to the process of designing and optimizing drug formulations using digital tools and collaborative technologies, allowing scientists to work from locations outside of traditional laboratories. This approach enables teams to conduct research, run simulations, analyze data, and collaborate on formulation projects without being physically present in the same facility. Advances in software, cloud computing, and secure data sharing have made remote work more feasible in the pharmaceutical industry, improving flexibility and access to global expertise. However, certain aspects such as hands-on laboratory testing may still require physical presence or coordination with on-site teams.

What are the key skills and qualifications needed to thrive in remote pharmaceutical formulation development?

To thrive in Remote Pharmaceutical Formulation Development, you need a solid background in pharmaceutical sciences, chemistry, or related fields, often supported by an advanced degree and industry experience. Familiarity with formulation software, laboratory information management systems (LIMS), and regulatory documentation tools is commonly required. Strong problem-solving abilities, attention to detail, and effective virtual communication are crucial soft skills for remote collaboration and innovation. These competencies ensure the efficient development of safe, effective drug formulations while maintaining regulatory compliance in a remote work environment.

What are some common challenges faced in remote pharmaceutical formulation development, and how can they be addressed?

One of the main challenges in remote pharmaceutical formulation development is effective communication and collaboration between cross-functional teams, as much of the work relies on sharing complex data and iterative feedback. To address this, teams often utilize advanced project management and data-sharing platforms, as well as regular video conferences to ensure alignment. Another challenge can be limited access to laboratory equipment; companies may use contract research organizations (CROs) or coordinate on-site visits for critical experiments. Staying organized and proactive in documenting progress is essential for remote success in this highly regulated field.

What is the difference between Remote Pharmaceutical Formulation Development vs Remote Pharmaceutical Quality Assurance?

AspectRemote Pharmaceutical Formulation DevelopmentRemote Pharmaceutical Quality Assurance
Required CredentialsDegree in Pharmacy, Chemistry, or related field; experience in formulationDegree in Pharmacy, Chemistry, or related field; experience in QA processes
Work EnvironmentLaboratories, R&D teams, collaborative virtual meetingsQuality labs, compliance teams, virtual audits
Employer & Industry UsagePharmaceutical R&D companies, biotech firmsPharmaceutical manufacturing, biotech, regulatory agencies
Search & Comparison IntentUnderstanding formulation roles, remote formulation jobsQA roles, remote quality assurance positions

Remote Pharmaceutical Formulation Development focuses on creating and optimizing drug formulations, often involving laboratory work and R&D collaboration. Remote Pharmaceutical Quality Assurance emphasizes ensuring product quality, compliance, and regulatory standards, typically involving audits and documentation. Both roles require similar educational backgrounds but differ in daily tasks and focus areas within the pharmaceutical industry.

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Cities with the most Remote Pharmaceutical Formulation Development job openings:

What are the most commonly searched types of Pharmaceutical Formulation Development jobs?

The most popular types of Pharmaceutical Formulation Development jobs are:

What states have the most Remote Pharmaceutical Formulation Development jobs?

States with the most job openings for Remote Pharmaceutical Formulation Development jobs include:

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For Remote Pharmaceutical Formulation Development jobs, the most frequently searched job titles are:

Remote Pharmaceutical Formulation Development jobs near you
Infographic showing various Remote Pharmaceutical Formulation Development job openings in the United States as of September 2026, with employment types broken down into 94% Full Time, 3% Part Time, and 3% Contract. Highlights an 100% Remote job distribution, with an average salary of $105,849 per year, or $50.9 per hour.

CMC Consultant

Remote

Atomic
See more jobs at Atomicexternal

Contractor

Re-posted 23 days ago

Job description

About Us:
Indomo is a clinical stage therapeutics company transforming clinic-based procedures into at-home care via device-enabled therapeutics. Indomo's lead program couples a proven corticosteroid with an innovative intradermal self-injection device to create the first fast-acting at-home solution for inflammatory acne lesions.
Position Overview:
Indomo is seeking an experienced CMC consultant to execute Chemistry, Manufacturing & Controls (CMC) strategy and operations on a fractional basis. This individual will play a critical role in advancing our lead asset through the NDA pathway by guiding CMC development, managing external partners, and ensuring regulatory readiness.
This role is ideal for a senior CMC expert who thrives in a hands-on, advisory + execution capacity and is comfortable working closely with a lean internal team and external CDMOs. The consultant will provide both strategic direction and tactical oversight across drug product development, analytical strategy, and integration with our device-enabled delivery system.
Key Responsibilities:
CMC Strategy
  • Help define and execute the overall CMC development strategy to support clinical progression and trial readiness
  • Support outsourced drug substance and drug product development with CDMO, including formulation optimization, stability, and device compatibility
  • Establish critical quality attributes, specifications, and acceptance criteria
  • Guide analytical method development, validation, and lifecycle management

External Vendor & Manufacturing Oversight
  • Interface with external stakeholders, including CDMOs, CROs, and suppliers.
  • Support selection, onboarding, and management of external partners.
  • Review deliverables, ensure timelines are met, and mitigate technical risks.
  • Advise on quality systems and inspection readiness.

Regulatory Support
  • Partner with regulatory team to shape CMC strategy for IND submission.
  • Organize execution of and contribute to regulatory documents (IND, briefing packages, NDA modules).
  • Prepare for and support FDA interactions (e.g., IND, EOP2, Type C meetings).

Qualifications:
Required
  • Advanced degree (Ph.D. preferred) in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related field.
  • 10+ years of drug development experience with demonstrated leadership of CMC strategy in biotech/pharmaceutical settings.
  • Expertise in formulation development, analytical method development/validation, stability programs, GMP manufacturing, and quality compliance.
  • Strong knowledge of FDA regulations, GMP guidelines, and global regulatory requirements.
  • Strong track record supporting INDs and/or NDAs.
  • Ability to operate independently in a fast-paced, dynamic startup environment.

Preferred
  • Experience with combination products (drug + delivery device).
  • Successful prior interactions with FDA on CMC topics.
  • Experience supporting programs from early clinical through late-stage development.

Why Join Indomo:
  • Opportunity to shape CMC strategy for an innovative combination product.
  • High-impact role with direct access to leadership and decision-making.
  • Collaborative, mission-driven team.
  • Flexibility in working style and scope.

We are focused on building a diverse and inclusive workforce. If you're excited about this role, but do not meet 100% of the qualifications listed above, we encourage you to apply.
Atomic is an Equal Opportunity Employer and considers applicants for employment without regard to race, color, religion, sex, orientation, national origin, age, disability, genetics or any other basis forbidden under federal, state, or local law.
Please review our CCPA policies here.

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