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Remote Pharmaceutical Formulation Development Jobs

Quotient Sciences

... formulation development, clinical pharmacology, clinical trials, and commercial product ... Our proprietary and disruptive platform - "Translational Pharmaceutics ® " - integrates Drug ...

New

Atomic

Drug CMC Lead

$150K - $215K/yr

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

Otsuka

Associate Director, Material Science

Support prototype formulation development (e.g., IR tablets, capsules) by providing material ... PhD in Materials Science, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related ...

Fuze Health

Verification Pharmacist - FuzeRx

Sharonville, OH · On-site +1

$53.50 - $64.25/hr

Operating in a remote capacity, the Verification Pharmacist supports remote verification functions ... dose, formulation, labeling, and patient instructions. Required Experience & Qualifications:

Alto

Verification Pharmacist - FuzeRx

Sharonville, OH · On-site +1

$53.50 - $64.25/hr

Operating in a remote capacity, the Verification Pharmacist supports remote verification functions ... dose, formulation, labeling, and patient instructions. Required Experience & Qualifications:

New

Southend Pharmacy

Medical Affairs Pharmacist - Remote

$59.50 - $71.75/hr

... Formulation rationale and excipient selection • Dosing, administration, and route-specific ... professional development • Engage in compliant scientific discussions with healthcare ...

Atomic

CMC Consultant

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

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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 Aug 22, 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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Remote Pharmaceutical Formulation Development jobs near you
Infographic showing various Remote Pharmaceutical Formulation Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $105,849 per year, or $50.9 per hour.

Associate Director/Director Pharmaceutical Development

BridgeBio Pharma

Remote

Full-time

Posted 17 days ago

Job description

What You'll Do

Provide strategic pharmaceutical development guidance as the CMC lead to cross functional project teams. 

Develop robust formulations and manufacturing processes to support development and rapid registration of QED products.

Review development and manufacturing programs at CRO's/external vendors to ensure compliance with agreed proposals, quality standards and timelines. Review external data.

Manage drug forecasts and any associated transactions

Integrate and liaise effectively with CMC team

Provide formulation and Clinical supply expertise/support in the preparation of regulatory submissions (e.g. IB, IND, NDA).

Responsibilities

Ability to work effectively and collaboratively on cross functional project teams, in a fast-paced, dynamic environment under tight timelines.

Develop complex formulation for pediatric indications.

Work effectively with CDMO's.

A team player, functional leader, effective listener, clear communicator and quick learner.

Clear, concise communication style with ability to interact internally and externally.

Willing to "roll up his/her sleeves and do what it takes" to achieve critical program deliverables.

Hands-on experience in clinical trials management/study conduct, formulation development and clinical trial manufacturing.

Knowledge of commercial manufacture

Where You'll Work

Remote with 30% travel expected

Who You Are

PhD or advanced degree in Chemistry or Pharmacy with 7+ years of bio/pharmaceutical industry experience in formulation development and Clinical Supply.

Expertise in formulation in addition to knowledge of PK/PD principles, ADME concepts, and regulatory documentation and authorship.

Knowledge of import/export sensitivities.

Demonstrated ability to manage Clinical Supply, Formulation development and manufacture at CRO's.

In-depth knowledge and understanding of CMC Regulatory requirements for US and EU are required

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