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Formulation Manager Jobs in Florida (NOW HIRING)

5TH HQ LLC

Formulator Assistant

Fort Lauderdale, FL · On-site

$25/hr

Maintain accurate formulation records and track development progress. * Write change controls and deviation documents related to formulations. * Communicate project updates to the R&D Manager ...

5TH HQ LLC

Formulator Assistant

Fort Lauderdale, FL · On-site

Maintain accurate formulation records and track development progress. * Write change controls and deviation documents related to formulations. * Communicate project updates to the R&D Manager ...

5TH HQ LLC

Formulator Assistant

Fort Lauderdale, FL · On-site

Maintain accurate formulation records and track development progress. * Write change controls and deviation documents related to formulations. * Communicate project updates to the R&D Manager ...

5TH HQ LLC

Formulator Assistant

Fort Lauderdale, FL · On-site

Maintain accurate formulation records and track development progress. * Write change controls and deviation documents related to formulations. * Communicate project updates to the R&D Manager ...

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Formulation Manager information

See Florida salary details

$10

$17

$31

How much do formulation manager jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for formulation manager in Florida is $17.06, according to ZipRecruiter salary data. Most workers in this role earn between $13.65 and $17.07 per hour, depending on experience, location, and employer.

What is a formulation manager?

Formulation Managers are professionals responsible for overseeing the development and optimization of product formulations, particularly in industries like pharmaceuticals, cosmetics, food, and chemicals. They lead teams to design, test, and refine product mixtures to meet quality, safety, and regulatory standards. Their role often involves coordinating with research, production, and quality assurance departments to ensure that product formulations are effective, stable, and cost-efficient. Formulation Managers also stay updated on industry trends and regulatory changes to keep their company's products competitive. Effective communication, project management, and technical expertise are key skills for this role.

What are some common challenges faced by a formulation manager in coordinating cross-functional teams?

Formulation Managers often work closely with R&D, quality assurance, regulatory, and production teams to bring new products from concept to launch. A common challenge is ensuring clear communication and alignment across departments, especially when dealing with tight timelines or shifting project priorities. Balancing technical requirements, regulatory compliance, and manufacturing feasibility can also be demanding. Successful Formulation Managers are proactive in problem-solving and skilled at fostering strong collaboration to keep projects on track.

What are the key skills and qualifications needed to thrive as a formulation manager, and why are they important?

To thrive as a Formulation Manager, you need a solid background in chemistry, pharmaceutical sciences, or a related field, often supported by an advanced degree and experience in product formulation. Familiarity with laboratory equipment, formulation development software, and regulatory compliance systems is typically required. Strong leadership, problem-solving, and project management skills help you effectively lead teams and navigate complex product development cycles. These competencies are crucial for ensuring product quality, regulatory adherence, and timely delivery of innovative formulations.

What is the difference between Formulation Manager vs Formulation Scientist?

AspectFormulation ManagerFormulation Scientist
CredentialsBachelor's or Master's in Chemistry, Pharmacy, or related field; often requires experience in project managementBachelor's or Master's in Chemistry, Pharmacy, or related field; focus on research skills
Work EnvironmentOversees teams in R&D or manufacturing settings, manages projects, and coordinates formulation developmentConducts laboratory research, experiments, and formulation testing
Industry UsageCommonly used in pharmaceutical, cosmetics, and chemical industries for leadership rolesPrimarily used in research and development departments for formulation development

The Formulation Manager typically oversees formulation projects, manages teams, and ensures product development aligns with business goals. In contrast, the Formulation Scientist focuses on conducting experiments and developing formulations in the lab. Both roles require similar educational backgrounds but differ in responsibilities and scope within the formulation process.

What are popular job titles related to Formulation Manager jobs in Florida?

For Formulation Manager jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Formulation Manager jobs in Florida look for?

The top searched job categories for Formulation Manager jobs in Florida are:

What cities in Florida are hiring for Formulation Manager jobs?

Cities in Florida with the most Formulation Manager job openings:

Formulation Manager jobs near you
Infographic showing various Formulation Manager job openings in Florida as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $35,487 per year, or $17.1 per hour.

Senior Director of Analytical Development

Syncromune

Fort Lauderdale, FL • On-site, Remote

$250K - $275K/yr

Full-time

Re-posted 20 days ago

Job description

The Senior Director of Analytical Development is responsible for providing strategic and operational leadership for all analytical development and analytical quality control activities supporting late-phase drug substance development, drug product formulation discovery, and drug product manufacturing and formulation development within the CMC group. This role oversees analytical method development, qualification, validation, transfer, and lifecycle management for single- and multi-component biological products, with emphasis on antibodies and oligonucleotides.
The Senior Director will lead and develop an internal analytical organization, directly managing a team of Managers, Associate Directors, and Director across method development and analytical QC, while providing technical and managerial oversight of external CROs, CMOs, and testing laboratories. The position requires close collaboration with formulation, manufacturing, quality, regulatory, and project teams to ensure phase-appropriate, compliant, and efficient analytical strategies that support clinical and future commercial development
Principal Duties and Responsibilities include the following:
Strategic and Technical Leadership
  • Define and execute the analytical development and analytical QC strategy across drug substance and drug product programs, ensuring alignment with CMC, regulatory, and corporate objectives.
  • Provide scientific and technical leadership for analytical methods supporting identity, purity, potency, content, impurities, degradation products, and stability of biological drug substances and drug products, including multi-component combinations.
  • Establish phase-appropriate analytical control strategies for late-phase development, including in-process controls, release testing, and stability programs.
  • Drive CQA generation and support QTPP development for late-stage project development .
  • Drive control of product specifications in collaboration with other functional groups.
  • Oversee development and implementation of novel or non-standard analytical approaches required for complex biological products.
People and Organization Leadership
  • Directly oversee and develop a team of at least four professionals at the Manager to Sr. Director level, including: Method Development and Analytical Quality Control, including stability, testing records, and data analysis
  • Set clear objectives, provide coaching and mentorship, conduct performance evaluations, and support professional development of the analytical team.
  • Ensure effective coordination and workload prioritization across method development and analytical QC functions.
Method Development, Validation, and Lifecycle Management
  • Oversee analytical method development, qualification, validation, transfer, and supplemental validation activities across internal and external laboratories.
  • Ensure robust implementation, execution, troubleshooting, and continuous improvement of core analytical and bioanalytical assays.
  • Review and approve analytical protocols, reports, SOPs, and technical documentation suitable for regulatory submission.
Analytical Quality Control and Stability Oversight
  • Provide leadership and oversight for analytical QC activities, including GMP testing, stability studies, data trending, and lifecycle monitoring.
  • Manage product and raw material specifications and product shelf-life/stability protocols.
  • Ensure appropriate oversight of stability protocols, shelf-life assignments, data review, and interpretation in support of late-phase programs.
  • Oversee review of testing records, analytical data packages, Certificates of Analysis, and investigation reports.
  • Lead or support investigations related to OOS, OOE, deviations, and analytical discrepancies, including root cause analysis and corrective actions at CROs/CMOs.
External Partner and Vendor Oversight
  • Manage and oversee analytical activities performed by CROs, CMOs, and external testing laboratories, ensuring quality, timelines, and cost control.
  • Provide technical oversight and decision-making support for outsourced analytical development, validation, and QC activities in a virtual operating model.
  • Participate in vendor selection, scope definition, budgeting, and performance management.
Regulatory and Compliance Support
  • Author, review, and approve analytical sections of CMC documentation for INDs, BLAs, and other regulatory submissions.
  • Ensure compliance with cGMP, GLP, ICH guidelines, FDA guidance, and relevant pharmacopeial standards.
  • Partner closely with Quality and Regulatory Affairs to support inspections, audits, and regulatory interactions.
Cross-Functional Collaboration
  • Collaborate closely with formulation discovery and development, drug substance and drug product development, drug substance and drug product manufacturing, quality, regulatory, and project management teams.
  • Provide analytical expertise to support formulation discovery, formulation development, process characterization, and late-phase manufacturing activities.
Supervisory Responsibilities:
  • Direct reports: Managers to Associate Directors within Method Development and Analytical Quality Control.
  • Indirect Reports: supervise activities at CMOs, CROs and external resources (i.e. consultants)
Qualification Requirements
Education:
  • Master or PhD in Chemistry, Biochemistry, or Analytical Science
Experience:
  • At least 15 years of experience in analytical development and validation activities for biologicals, including product development and manufacturing.
  • Experience with liquid biological injectable dosage forms, drug formulations of individual and combination products, is highly preferred.
  • Experience with analytical techniques applicable for characterization of proteins, antibodies and/or oligonucleotides highly preferred.
  • Experience in complex single or tandem mass-spectrometry technologies used for characterization of proteins, oligonucleotides and their impurities is highly valued.
  • Comprehensive understanding of the dosage form manufacturing process development, scale-up, optimization and validation processes.
  • Strong scientific and operational background in the optimization and validation of compendial, biochemistry, HPLC, immunochemical and cell-based assays
  • Proven ability to provide analytical expertise on programs/project teams for pre-clinical and clinical studies with a wide variety of techniques and technologies.
  • Experience working in a GMP/GLP regulated environment and deep understanding of phase appropriate method qualification, validation, sample analysis, GLP, GMP requirements, ICH guidelines and FDA guidance.
  • Experience authoring and reviewing IND and/or BLA submissions.
  • Expert knowledge of advanced principles, concepts, and theory related to product and process development.
  • Experience in preparing budget and managing expenses.
  • Skilled at managing CROs and CDMOs.
Knowledge/Skill:
  • Strong leadership, organizational, and project management skills.
  • Excellent written and verbal communication skills; strong technical writing and document review capabilities.
  • Ability to operate effectively in a remote and virtual work environment.
  • Demonstrated ability to collaborate across cross-functional and geographically distributed teams.
  • Detail-oriented with exceptional documentation practices.
  • Knowledge of U.S. and Chinese Pharmacopeia methods for biologic drugs is a plus.
  • Proficiency in English required; Mandarin proficiency is a plus.
  • Flexibility to travel domestically and internationally as needed.
Working Conditions:
  1. Specify work environment:
  • Work from home.
  • Support collaboration with non-U.S. CDMO partners by accommodating meetings outside core working hours, including early morning, evening and/or nighttime sessions when necessary
  • Domestic and international travel up to 25%.
  • Regularly required to stand, sit, talk, hear, and use hands, with 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: $250-$280K
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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