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Director Formulation Development Jobs in Florida

... Development & Regulatory Director. Communicate regularly with President and associated Supervisor/Manager, provide detailed up-to-date reports on current and new formulation, materials ...

... Development & Regulatory Director. Communicate regularly with President and associated Supervisor/Manager, provide detailed up-to-date reports on current and new formulation, materials ...

... Development & Regulatory Director. Communicate regularly with President and associated Supervisor/Manager, provide detailed up-to-date reports on current and new formulation, materials ...

Product Development & Innovation * Lead formulation and development of dressings, sauces, bakery items, and cold-pressed juices. * Translate culinary concepts into scalable, commercially viable ...

Product Development & Innovation * Lead formulation and development of dressings, sauces, bakery items, and cold-pressed juices. * Translate culinary concepts into scalable, commercially viable ...

... of direct end customer engagement, the ABB EL Rep Network, ABB's C&I, OEM, and Utility Sales ... Provide sales leadership in assigned geography through the formulation and execution of strategies ...

Contributes significantly to the formulation of care delivery policies and procedures. * Manages ... Participates in and leads future development initiatives for the organization. * Provides direct ...

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R&D Lab Technician

Tampa, FL · On-site

$26 - $28/hr

... direct supervision of selected lab chemists. This position will involve hands-on support of R&D ... supporting formulation tasks. * Manufacture lab-scale batches of insulation and adhesive ...

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R&D Laboratory Technician

Tampa, FL · On-site

$26 - $28/hr

... direct supervision of selected lab chemists. This position will involve hands-on support of R&D ... supporting formulation tasks. * Manufacture lab-scale batches of insulation and adhesive ...

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Director Formulation Development information

See Florida salary details

$66.5K

$143K

$214.8K

How much do director formulation development jobs pay per year?

As of May 31, 2026, the average yearly pay for director formulation development in Florida is $143,041.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,200.00 and $186,100.00 per year, depending on experience, location, and employer.

What is a Director Formulation Development job?

A Director of Formulation Development leads the design and optimization of pharmaceutical formulations, ensuring they meet quality, regulatory, and performance standards. They oversee research, guide teams in developing new drug delivery systems, and collaborate with regulatory and manufacturing teams. This role requires expertise in chemistry, pharmaceutics, and process development to ensure successful product commercialization. Additionally, they manage project timelines, budgets, and technical challenges to drive innovation in drug formulation.

What are the key skills and qualifications needed to thrive in the Director Formulation Development position, and why are they important?

A Director Formulation Development typically requires an advanced degree in pharmaceutical sciences, chemistry, or a related field, along with significant experience in drug formulation and team management. Familiarity with industry-standard formulation software, regulatory compliance systems, and relevant certifications such as PMP or Six Sigma are highly valued. Excellent leadership, communication, and strategic planning skills help set high performers apart in this role. These skills and qualities are critical for driving innovative product development, ensuring regulatory compliance, and effectively leading cross-functional teams.

What are the major responsibilities and day-to-day activities for a Director Formulation Development?

As a Director Formulation Development, you will oversee the design and optimization of drug formulations, lead a multidisciplinary team of scientists, and ensure that projects meet quality, budget, and timeline expectations. Your daily activities often include strategic planning, reviewing progress reports, troubleshooting formulation challenges, and collaborating with regulatory, manufacturing, and quality assurance departments. You may also interact with upper management to report on key milestones and contribute to long-term product development strategies. This role offers opportunities to influence project pipelines and play a central part in bringing new therapies to market.
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Posted 13 days ago


Inteplast rating

6.0

Company rating: 6.0 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

96th of 109 rated packaging manufacturers


Job description

TITLE: Sr. Formulator Lead

POSITION OBJECTIVE:  Responsible for the evaluation and development of nutraceutical formulas and formulation functions throughout the entire process of manufacturing and production, by product specification, following cGMP's and Standard Operation Processors.  Follow and ensures personnel comply with established procedures including standard operating procedures (SOP’s), cGMPs, food safety regulations, and safety procedures.

 

QUALIFICATIONS:

  • Ensure consistent, dependable attendance and demonstrate a willingness to accommodate non-standard work hours as necessary.
  • Capable of effectively managing job-related stress and fostering productive workplace interactions.
  • Requires 4 years of practical experience in nutraceutical or pharmaceutical formulation, R&D or related functions in a nutraceutical or pharmaceutical environment.  Flavoring knowledge and experience required.
  • Working knowledge of pharmaceutical or nutraceutical formulation and R&D processes and techniques, including but not limited to good working knowledge of formulation, sampling and testing techniques and systems, solid dosage equipment and dosage form development, good knowledge of math, computer literacy, good written and oral communication skills, high degree of organizational skills and attention to detail. 
  • Experience of flavoring theoretically/practically regarding various product forms such as gummies, chewable tablets, powders and/or soft chews required.
  • Associate or bachelor’s degree in chemistry, Chemical Engineering, Pharmaceutical Science or other closely related discipline.

JOB RESPONSIBILITIES:

  • Report directly to the Product Development & Regulatory Director. Communicate regularly with President and associated Supervisor/Manager, provide detailed up-to-date reports on current and new formulation, materials, specifications, OOS items or issues to improve current products and develop new products.
  • Perform all assigned formulation tasks timely and accurately. Evaluate current formulas, help develop new formulas by evaluating new and alternate sources of raw materials, seek cost savings alternatives.
  • Provide support to QC, including but not limited to process improvement, consistency and accuracy of processes, cost savings initiatives, troubleshooting, rework processes, development of prototypes, production of trial samples, scientific review and specification of raw materials.
  • Maintain all required Standards of Quality throughout the entire process. Follow cGMP's, SOP's, MSDS specifications, Sampling and Formulation Plans, Safety in the Workplace Best Practices, OOS Best Practices.
  • Report any out-of-compliance items to the supervisor immediately.
  • Demonstrate a successful track record in the improvement of current products and in the development of new solid dosage nutraceutical products.
  • Identifies any deficiencies, constraints and/or problems that could impede the efficient process flow and assist and/or provide ideas and feedback to solve them.
  • May be required to perform other duties as requested, directed or assigned.
  • To lead and execute along with other Senior Formulators within the organization to meet formulation/quoting deadlines and to aid the department as needed regarding any Product Development activities.
  • Must adhere to Standard Operating Procedures (SOP's) and current Good Manufacturing Practices (cGMP's) meet all operational requirements as specified by regulatory standards.
  • Responsible for the process of evaluating current formulas and assisting with the development of new formulas for current and future products.
  • Perform data retrieval, data analysis and reporting via use of Information Management Systems and/or Quality Management Systems, or applicable internal reporting system.
  • Assist with the evaluation of new and alternate raw materials to improve current products and develop new products.
  • Communicate with manufacturing, production and packaging personnel to identify and correct quality assurance issues throughout the process.
  • Responsible for external communication with clients, external partners, etc. as required and as directed by the Product Development Director.
  • Continually assess proper equipment set-up and operational issues, communicating same with off shift personnel and supervisor.

 

MACHINES, TOOLS, EQUIPMENT, ELECTRONIC DEVICES & SOFTWARE:

  • Proficient with MS Office Suit (Word, Excel, PowerPoint & Outlook)

 


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