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Pharmaceutical Formulation Remote Jobs (NOW HIRING)

Strive Pharmacy

L&D LMS Administrator

Mesa, AZ · Remote

Every formulation we prepare is built to the specific needs of a specific person, and every ... Position Type: Full time, remote Position Overview: An individual must be able to manage our ...

Vrtx

MS&T Senior Manager - Drug Product

Boston, MA · On-site +1

$138K - $208K/yr

... formulation and compounding, sterile filtration, aseptic filling, visual inspection, and packaging ... Provideonthefloorand remote MS&T support during manufacturing campaigns. * Partner with Operations ...

ABB

Business Development Manager

FL · Remote

Remote, [#LI-Remote] in southern half of Florida. This role requires the candidate to live and ... Provide sales leadership in assigned geography through the formulation and execution of strategies ...

ABB

Business Development Manager

Tampa, FL · Remote

Remote, [#LI-Remote] in southern half of Florida. This role requires the candidate to live and ... Provide sales leadership in assigned geography through the formulation and execution of strategies ...

OneDigital

Clinical Account Executive - Remote

$120K - $130K/yr

... formulation and presentation of the RFP results to prospects and clients * Effectively present ... Active licensure as a pharmacist * Prior experience or understanding of the PBM industry is ...

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Pharmaceutical Formulation Remote information

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How much do pharmaceutical formulation remote jobs pay per hour?

As of Jul 8, 2026, the average hourly pay for pharmaceutical formulation remote in the United States is $22.83, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $22.84 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Formulation Scientist in a remote role, and why are they important?

To thrive as a Pharmaceutical Formulation Scientist working remotely, you need a solid background in pharmaceutical sciences or chemistry, often supported by a relevant degree and industry experience in drug formulation. Familiarity with formulation software (such as Design of Experiments tools), data analysis programs, and regulatory documentation systems is typically required. Outstanding problem-solving, communication, and self-motivation skills set top candidates apart in a remote setting. These skills and qualifications are crucial for ensuring effective development, documentation, and cross-functional collaboration in pharmaceutical product creation, even when working off-site.

What is a Pharmaceutical Formulation Remote job?

A Pharmaceutical Formulation Remote job involves developing and optimizing drug formulations while working outside of a traditional laboratory or office setting, typically from home. Professionals in this role use scientific expertise to design, analyze, and improve the composition, stability, and delivery of pharmaceutical products. They often collaborate with cross-functional teams, document research findings, and ensure formulations meet regulatory requirements, all through digital communication and data analysis tools. This position is ideal for individuals seeking flexibility and who have experience in pharmaceutical sciences, chemistry, or related fields.

What are some typical challenges faced when working remotely in pharmaceutical formulation, and how can they be addressed?

One common challenge in remote pharmaceutical formulation roles is effective collaboration with laboratory and cross-functional teams, as much of the work depends on real-time data and physical sample evaluations. To address this, professionals often rely on robust digital communication tools, regular virtual meetings, and clear documentation to stay aligned with on-site colleagues. Maintaining organized records and proactively scheduling check-ins helps ensure timely feedback and project continuity. Additionally, remote workers should familiarize themselves with digital platforms for data sharing and project management to stay efficient and connected.

What is the difference between Pharmaceutical Formulation Remote vs Pharmaceutical Quality Control Remote?

AspectPharmaceutical Formulation RemotePharmaceutical Quality Control Remote
Primary FocusDeveloping and optimizing drug formulationsTesting and ensuring the quality of pharmaceutical products
Required SkillsFormulation science, lab techniques, regulatory knowledgeAnalytical testing, quality assurance, compliance standards
Work EnvironmentResearch labs, development teams, remote collaborationLaboratories, testing facilities, remote data analysis
Common CertificationsDegree in pharmacy, pharmaceutical sciences, or chemistryDegree in pharmacy, chemistry, or related field; certifications in quality assurance

Pharmaceutical Formulation Remote and Pharmaceutical Quality Control Remote roles both operate within the pharmaceutical industry but focus on different aspects. Formulation specialists develop new drug products, while quality control professionals ensure products meet safety and efficacy standards. Both roles often require similar educational backgrounds and can be performed remotely, but their daily tasks and objectives differ significantly.

More about Pharmaceutical Formulation Remote jobs
What cities are hiring for Pharmaceutical Formulation Remote jobs? Cities with the most Pharmaceutical Formulation Remote job openings:
What are the most commonly searched types of Pharmaceutical Formulation jobs? The most popular types of Pharmaceutical Formulation jobs are:
What states have the most Pharmaceutical Formulation Remote jobs? States with the most job openings for Pharmaceutical Formulation Remote jobs include:
What job categories do people searching Pharmaceutical Formulation Remote jobs look for? The top searched job categories for Pharmaceutical Formulation Remote jobs are:
Pharmaceutical Formulation Remote jobs near you
Infographic showing various Pharmaceutical Formulation Remote job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $47,488 per year, or $22.8 per hour.
Associate Director, CMC Analytical Development, Separation

Associate Director, CMC Analytical Development, Separation

Syncromune

Fort Lauderdale, FL • Remote

$165K - $200K/yr

Full-time

Posted 12 days ago

Job description

The Associate Director of CMC Analytical Development will oversee the execution of the analytical strategy for drug substance and drug product development across all phases of clinical development and commercialization. This role is responsible for overseeing method development, validation, transfer, and lifecycle management to ensure compliance with regulatory requirements and alignment with company objectives.
Principal Duties and Responsibilities include the following:
  • Define and implement analytical development strategies to support CMC programs from early development through commercialization.
  • Provide technical leadership in analytical sciences, including chromatography, spectroscopy, and characterization techniques.
  • Guide analytical development activities at CDMO and CTL, including method development, optimization, transfer, validation, troubleshooting, and lifecycle management for GMP test methods for DS and DP.
  • Guide extended characterizations in support of comparability and regulatory applications.
  • Foster collaboration with cross-functional groups including Process Development, Quality, and Regulatory Affairs.
  • Author and review analytical sections of regulatory submissions (IND, IMPD, NDA, BLA).
  • Ensure adherence to GMP, ICH, and FDA guidelines for analytical activities.
  • Drive continuous improvement and innovation in analytical technologies and processes.
Supervisory Responsibilities:
  • Indirect Reports: supervise CDMO, CTL, and external resources (such as consultants)
Qualification Requirements:
Education:
  • Ph.D. or M.S. degree in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field.
Experience:
  • Must have 5+ years of pharmaceutical or biotechnology industry experience specializing in analytical development.
  • Must have working knowledge of cGMP, ICH, and regulatory guidelines.
  • Must have hands-on experience managing global CTLs and CDMOs.
  • Must have strong technical expertise in separation science, such as liquid chromatography or mass spectrometry.
  • Must have strong technical experience in at least one of the modalities: monoclonal antibody and/ or oligonucleotide.
  • Must have experience in method development, validation, and lifecycle management for QC methods.
  • Good to have experience in complex drug products, such as co-formulation, multi-components, conjugates, etc.
  • Good to have experience in extended characterization & comparability studies to support BLA submission.
  • Good to have experience in authoring technical and scientific documents for regulatory submissions, including IND and BLA filings.
  • Good to have late phase experience, such as PPQ and commercialization.
  • Candidates proficient in both English and Mandarin are highly encouraged to apply.
  • Ability to work in a fast-paced virtual environment.
  • Flexibility to travel domestically and internationally as required.
  • Excellent communication, leadership, organizational and project management skills.
Working Conditions:          
  1. Specify work environment:
  • Work from home.
  • Domestic and international travel up to 25%.
  • Regularly required to stand, sit, talk, hear, and use hands
  • Prolonged periods of sitting and standing

Syncromune is an Equal Opportunity Employer.

The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to, the primary work location and the chosen candidate’s relevant skills, experience, and education.

Expected US salary range:  $165-$200K

This position generally is eligible for cash incentive compensation, equity incentive compensation, and employee benefits under the Company’s benefit plans. 

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