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Remote Formulation Scientist Jobs in Florida (NOW HIRING)

micro1 AI

Digital Chemistry Specialist - Remote

Tampa, FL · Remote

$90 - $120/hr

Bioinformatics Scientist Role Type: Contractor Location: Remote micro1 is engaging Bioinformatics Scientists to contribute their specialized expertise to a customer's innovative project. In this role ...

micro1 AI

Digital Chemistry Specialist - Remote

Miami, FL · Remote

$90 - $120/hr

Bioinformatics Scientist Role Type: Contractor Location: Remote micro1 is engaging Bioinformatics Scientists to contribute their specialized expertise to a customer's innovative project. In this role ...

micro1 AI

Digital Chemistry Specialist - Remote

Davie, FL · Remote

$90 - $120/hr

Bioinformatics Scientist Role Type: Contractor Location: Remote micro1 is engaging Bioinformatics Scientists to contribute their specialized expertise to a customer's innovative project. In this role ...

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All JobsFormulation Scientist JobsRemote Formulation Scientist JobsRemote Formulation Scientist Jobs in Florida

Remote Formulation Scientist information

What is the difference between Remote Formulation Scientist vs Remote Quality Control Analyst?

AspectRemote Formulation ScientistRemote Quality Control Analyst
Required CredentialsBachelor's/Master's in Chemistry, Pharmacy, or related field; experience in formulation developmentBachelor's in Chemistry, Biology, or related; experience in quality testing and analysis
Work EnvironmentLaboratories, R&D teams, pharmaceutical or biotech companiesLaboratories, manufacturing facilities, quality assurance teams
Industry UsagePharmaceutical, biotech, cosmetics, food industriesPharmaceutical, biotech, food, and consumer goods industries
Common Search/ComparisonYesYes

The Remote Formulation Scientist focuses on developing and optimizing product formulations, often working in R&D settings within pharmaceutical, biotech, or cosmetic industries. In contrast, the Remote Quality Control Analyst primarily conducts testing and analysis to ensure product quality and compliance. Both roles require relevant scientific credentials and are integral to product development and quality assurance processes in similar industries.

What are the most commonly searched types of Formulation Scientist jobs in Florida? The most popular types of Formulation Scientist jobs in Florida are:
What are popular job titles related to Remote Formulation Scientist jobs in Florida? For Remote Formulation Scientist jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Remote Formulation Scientist jobs in Florida look for? The top searched job categories for Remote Formulation Scientist jobs in Florida are:
What cities in Florida are hiring for Remote Formulation Scientist jobs? Cities in Florida with the most Remote Formulation Scientist job openings:
Remote Formulation Scientist jobs near you
Infographic showing various Remote Formulation Scientist job openings in Florida as of July 2026, with employment types broken down into 73% Full Time, and 27% Contract. Highlights an 100% Remote job distribution.

Associate Director/Director, CMC Analytical Development, Separation

Syncromune

Fort Lauderdale, FL • On-site, Remote

$165K - $200K/yr

Full-time

Re-posted 10 days ago

Job description

The Associate Director/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 8+ 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 for Assoc Director and Director levels: $165-$245K
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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