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Formulation Jobs in Kentucky (NOW HIRING)

The ideal candidate has foundational knowledge in chemistry, surfactants, materials, or formulation science, inorganic and organic coating technologies, and is excited to apply scientific principles ...

The ideal candidate has foundational knowledge in chemistry, surfactants, materials, or formulation science, inorganic and organic coating technologies, and is excited to apply scientific principles ...

Lead the formulation development and commercialization of high-performance greases and industrial fluids for OEM, Aramco Affiliate, and retail channels. * Provide global support to strategic ...

Lead the formulation development of new EV lubricant fluids including those for hybrid transmissions and battery electric vehicles by evaluating and selecting additives, base oils, and other ...

Lead the formulation development of new EV lubricant fluids including those for hybrid transmissions and battery electric vehicles by evaluating and selecting additives, base oils, and other ...

Lead the formulation development of new EV lubricant fluids including those for hybrid transmissions and battery electric vehicles by evaluating and selecting additives, base oils, and other ...

Lead the formulation development and commercialization of high-performance greases and industrial fluids for OEM, Aramco Affiliate, and retail channels. * Provide global support to strategic ...

Chemist

Henderson, KY ยท On-site

Provide quality testing, sampling, analysis, formulation, characterization to ensure quality/standards are being met. * Document quality activities to prove a record of quality compliance efforts

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Showing results 1-20

Formulation information

See Kentucky salary details

$12

$19

$36

How much do formulation jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for formulation in Kentucky is $19.83, according to ZipRecruiter salary data. Most workers in this role earn between $15.87 and $19.86 per hour, depending on experience, location, and employer.

What does a formulation scientist do?

A formulation scientist is responsible for developing and optimizing mixtures of ingredients to create products such as pharmaceuticals, cosmetics, or food items. They ensure that the formulated product is stable, effective, and meets quality standards. This role involves research, testing, and collaboration with other scientists to bring safe and effective products to market. Formulation scientists often work in laboratory settings and are involved in scaling up production from small batches to mass manufacturing.

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

To thrive as a Formulation Scientist, you need a strong background in chemistry, pharmaceuticals, or chemical engineering, often supported by a relevant degree. Familiarity with laboratory instrumentation, formulation development software, and regulatory standards such as GMP is typically required. Attention to detail, problem-solving abilities, and effective communication are vital soft skills for this role. These competencies ensure the safe, efficient, and compliant development of new products in industries like pharmaceuticals and cosmetics.

What are some common challenges faced by professionals in formulation roles, and how can they be addressed?

Professionals in formulation often encounter challenges such as achieving product stability, optimizing ingredient compatibility, and ensuring regulatory compliance. These issues require strong problem-solving skills, continuous testing, and close collaboration with analytical, quality assurance, and regulatory teams. Staying up-to-date with new ingredients, technologies, and industry standards can help address these challenges and support successful product development. Open communication and teamwork are also essential in troubleshooting and refining formulations.

What is the difference between Formulation vs Chemist?

AspectFormulationChemist
Required CredentialsDegree in Chemistry, Chemical Engineering, or related fieldDegree in Chemistry or Chemical Sciences
Work EnvironmentLaboratories, manufacturing plants, R&D centersLaboratories, research facilities, industrial settings
Industry UsageProduct development, formulation of compounds, cosmetics, pharmaceuticalsResearch, analysis, testing, and development of chemical substances
Common Search & ComparisonYesYes

Formulation specialists focus on developing and optimizing product recipes, while chemists conduct research and analysis of chemical substances. Both roles require chemistry degrees and often work in similar environments, but formulation emphasizes product development, whereas chemists may work more on research and testing.

What are the most commonly searched types of Formulation jobs in Kentucky? The most popular types of Formulation jobs in Kentucky are:
Infographic showing various Formulation job openings in Kentucky as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 1% Temporary, and 3% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $41,244 per year, or $19.8 per hour.
Senior Scientist I, Analytical Chemistry

Senior Scientist I, Analytical Chemistry

Kindeva Drug Delivery

Lexington, KY โ€ข On-site

$90K - $124K/yr

Full-time

Posted 4 days ago


Job description

Our Work Matters
At Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world.
Why Kindeva?
  • Purpose-driven work environment
  • Significant growth potential
  • Collaborative team culture
  • Direct impact on patient care
  • Industry-leading innovation

The Impact You Will Make
Transform Lives Through Scientific Innovation
Join a growing pharmaceutical CDMO where your expertise will directly support the development of innovative drug products that improve patient health worldwide.
As a Senior Scientist, Analytical Chemistry, you will serve as a technical leader within the R&D Analytical Chemistry group, leading analytical strategies that support pharmaceutical product development from early-stage development through commercialization. You will provide scientific leadership in method development, validation, verification, transfer, and troubleshooting activities while partnering with cross-functional teams to advance customer programs and internal development initiatives.
This role is ideal for a scientist who thrives in a fast-paced development environment, enjoys solving complex technical challenges, and is passionate about mentoring others while advancing analytical capabilities within a growing organization.
Growth Opportunity
Our Lexington site continues to experience significant growth across development and manufacturing programs. This position offers the opportunity to lead complex analytical projects, support innovative drug development programs, influence technical strategy, mentor junior scientists, and expand Kindeva's analytical capabilities while working closely with customers and internal development teams.
Responsibilities
Analytical Method Development & Validation
  • Lead the development, optimization, and validation of robust analytical methods for drug substances and drug products in accordance with ICH, USP, and regulatory guidelines.
  • Design and execute complex analytical studies to support formulation development, process development, stability programs, and customer projects.
  • Lead or support technology transfer of analytical methods to internal and external QC laboratories and CMOs.
  • Support qualification of new analytical laboratory equipment.
  • Implement new analytical techniques and instrumentation to expand internal capabilities.
  • Act as a subject matter expert (SME) for analytical technologies, method troubleshooting, and regulatory inspections.

Scientific Leadership & Technical Execution
  • Provide leadership and execution of complex scientific experiments.
  • Utilize creative thinking to generate solutions to complex technical problems.
  • Prioritize personal workload to ensure key objectives are achieved on time and within project expectations.
  • Stay current with advancements in analytical technologies, industry best practices, and regulatory expectations.
  • Mentor and provide technical oversight to junior scientists and analysts, ensuring scientific rigor and compliance with quality standards.

Documentation, Compliance & Regulatory Support
  • Author and review technical documents, including method validation protocols and reports, specifications, analytical development reports, and regulatory submissions (IND, NDA, ANDA, BLA).
  • Prepare and maintain accurate and timely laboratory records in accordance with company policies and regulatory requirements.
  • Ensure compliance with GMP requirements, regulatory expectations, and internal quality systems.
  • Support regulatory inspections, customer audits, and compliance initiatives as required.

Cross-Functional Collaboration & Business Support
  • Collaborate cross-functionally with Formulation Development, Process Development, Quality Assurance, Regulatory Affairs, Manufacturing, and customer teams to ensure successful product development.
  • Represent Analytical Chemistry in project meetings and customer meetings with limited supervision.
  • Contribute to continuous improvement initiatives and innovation within the analytical development function.
  • Support Marketing and Business Development activities through technical presentations, posters, publications, blogs, white papers, and industry conferences.
  • Support cross-functional training and execution of activities within the R&D Product Development & Design Team as needed.

Qualifications
  • PhD in a scientific discipline with 1+ years of relevant experience; Master's degree with 3+ years of experience; Bachelor's degree with 6+ years of experience; or 9+ years of equivalent experience without a degree.
  • In-depth experience with analytical techniques including HPLC, UPLC, GC, UV, FTIR, spray testing, compendial methods, and related analytical technologies.
  • Demonstrated success in analytical method development, optimization, validation, and troubleshooting under GMP and ICH guidelines.
  • Strong understanding of regulatory requirements and CMC components of pharmaceutical drug development.
  • Experience with stability testing, impurity/degradant characterization, and forced degradation studies.
  • Proven ability to lead technical projects and work effectively within cross-functional teams.
  • Strong written and verbal communication skills, including experience authoring technical and regulatory documentation.
  • Demonstrated ability to mentor, influence, and develop junior scientists and technical staff.
  • Experience with nasal spray drug products and device-related analytical testing is preferred.
  • Experience within pharmaceutical, biotechnology, contract development and manufacturing (CDMO), or regulated product development environments strongly preferred.

Physical Demands / Qualifications
  • Employee is required to regularly use hands in order to handle laboratory materials and supplies.
  • Employee is required to use computers for extended periods each day.
  • Employee is required to effectively communicate through both verbal and electronic means.
  • Employee is required to regularly stand and walk for extended periods of time.
  • Employee must occasionally lift and/or move up to 25 pounds.
  • Ability to use proper lifting techniques and remain aware of laboratory and workplace hazards.
  • Employee is required to follow all site safety procedures and wear appropriate PPE.

Join our One Team mission of manufacturing more tomorrows. Your scientific expertise will help advance innovative therapies and improve the health and well-being of patients around the world.
#LI-Onsite
California residents should review our Notice for California Employees and Applicants before applying.
Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees-regardless of format-without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
Do you see yourself as part of the Kindeva mission? Click Apply Now Today!