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Director Formulation Development Jobs in Kentucky

Supporting the development, optimization, and scaling of cannabis-infused edibles through bench ... Familiarity with GMPs, food safety, and regulatory requirements, with direct experience in sensory ...

Supporting the development, optimization, and scaling of cannabis-infused edibles through bench ... Familiarity with GMPs, food safety, and regulatory requirements, with direct experience in sensory ...

Lead the formulation development of new EV lubricant fluids including those for hybrid ... S. in Chemistry or Engineering Discipline with direct experience. * Masters or Doctorate in ...

Lead the formulation development of new EV lubricant fluids including those for hybrid ... S. in Chemistry or Engineering Discipline with direct experience. * Masters or Doctorate in ...

Lead the formulation development of new EV lubricant fluids including those for hybrid ... S. in Chemistry or Engineering Discipline with direct experience. * Masters or Doctorate in ...

Budget development, implementation, and maintenance. * Policy and procedure formulation, review, and revision. * Direct employee supervision and performance evaluations. 3. Compliance & Training:

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Director Formulation Development information

See Kentucky salary details

$77.3K

$166.2K

$249.7K

How much do director formulation development jobs pay per year?

As of Jul 10, 2026, the average yearly pay for director formulation development in Kentucky is $166,246.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,600.00 and $216,300.00 per year, depending on experience, location, and employer.

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.

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 popular job titles related to Director Formulation Development jobs in Kentucky? For Director Formulation Development jobs in Kentucky, the most frequently searched job titles are:
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What cities in Kentucky are hiring for Director Formulation Development jobs? Cities in Kentucky with the most Director Formulation Development job openings:
Infographic showing various Director Formulation Development job openings in Kentucky as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $166,246 per year, or $79.9 per hour.
Product Development Engineer

Product Development Engineer

Keystone & Golden, Inc.

Lexington, KY โ€ข On-site

Full-time

Posted 23 days ago


Job description

About the Company

Our client is a rapidly growing, investor-backed consumer wellness company that has quickly established itself as a category leader in functional oral pouch products. The company is pioneering innovative performance-focused products that deliver functional benefits through a convenient oral delivery format and is experiencing significant growth as the category continues to expand.

This is an opportunity to join a highly entrepreneurial organization during a pivotal stage of growth and play a key role in developing next-generation products from concept through commercialization.

Position Summary

The Product Development Engineer will be a core member of the company's R&D team, responsible for the full product development lifecycleโ€”from bench formulation and ingredient evaluation through scale-up, manufacturing transfer, and commercial launch.

This role combines formulation science, process development, sensory evaluation, and technical commercialization. The successful candidate will work closely with contract manufacturers, suppliers, quality, and operations teams to bring innovative products to market.

The ideal candidate is hands-on, technically strong, and comfortable operating in a fast-paced environment where creativity, problem-solving, and execution are equally important.

Key Responsibilities

Formulation Development

  • Develop and optimize formulations, flavor systems, and active ingredient delivery platforms.

  • Evaluate ingredients and excipients for functionality, stability, performance, and regulatory compliance.

  • Optimize product characteristics including pH, water activity, dissolution, and sensory performance.

  • Maintain detailed development records, batch documentation, and formulation specifications.

Ingredient & Supplier Evaluation

  • Source and evaluate new ingredients, flavors, excipients, and functional actives.

  • Review supplier documentation including COAs, SDSs, and technical specifications.

  • Assess ingredient quality, performance, and regulatory status.

  • Support qualification of new suppliers and raw materials.

Commercialization & Scale-Up

  • Lead technical transfer of formulations to manufacturing partners.

  • Develop manufacturing instructions, product specifications, and critical quality attributes.

  • Support pilot runs, scale-up activities, and commercial production trials.

  • Troubleshoot manufacturing challenges and drive resolution during commercialization.

  • Serve as a primary technical liaison with contract manufacturing partners.

Sensory & Product Performance

  • Design and execute sensory evaluations focused on taste, texture, mouthfeel, and overall product experience.

  • Analyze sensory data and identify opportunities for product improvement.

  • Translate consumer and panel feedback into formulation enhancements.

Quality & Regulatory Support

  • Assist with development of product specifications and testing protocols.

  • Support compliance with dietary supplement GMP requirements and internal quality standards.

  • Ensure development documentation supports successful commercialization and regulatory compliance.

Qualifications

Required

  • Bachelor's degree or higher in Food Science, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related scientific discipline.

  • 2+ years of hands-on formulation experience in oral pouch products or related oral delivery systems.

  • Experience supporting product scale-up and manufacturing transfer.

  • Strong technical writing and documentation skills.

  • Experience operating laboratory and analytical equipment independently.

  • Strong problem-solving and troubleshooting abilities.

Preferred

  • Experience with oral delivery technologies such as pouches, buccal, sublingual, lozenges, or dietary supplement delivery systems.

  • Sensory science or structured sensory panel experience.

  • Working knowledge of dietary supplement regulations and 21 CFR Part 111.

  • Experience with dissolution testing, release testing, or bioavailability-focused product development.

  • Experience working with contract manufacturers in a regulated environment.

Why Consider This Opportunity?

  • Join a category-leading, high-growth wellness company.

  • Work directly on innovative products from concept to launch.

  • Significant exposure to formulation, commercialization, manufacturing, and product strategy.

  • Highly entrepreneurial environment with direct impact on product success.

  • Opportunity to help shape the future of an emerging consumer health category.