Actalent
Senior Formulation Scientist (Actalent)
Location:
Valencia, CA Employment Type:
Full‑time, Permanent Seniority Level:
Mid‑Senior
The Research and Development Senior Formulation Scientist plays a critical role in the selection of ingredients, development and optimization of formulations for dietary supplements and food products. This position involves proper assessment of active and non‑active ingredients, experimental design, scientific judgement and the application of scientific principles to create high‑quality, stable, and efficacious product formulations that meet the outlined product profile.
Responsibilities
Selection of appropriate ingredients, development of paper formulations and reformulations that meet product profiles and development objectives.
Perform benchtop experiments for development of nutraceutical products (capsules, tablets, powders, stick packs), considering client requirements, manufacturing feasibility, ingredient compatibility, stability, solubility, and bioavailability.
Evaluate and select appropriate excipients and recommend alternate active ingredients for use in formulations based on scientific understanding and regulatory requirements.
Reformulate products to enhance appearance, taste, texture, solubility, stability, efficacy, and manufacturability with speed, accuracy and robustness.
Ensure that formulated products meet quality standards, regulatory guidelines, and industry best practices. Collaborate with regulatory and quality teams to address and resolve any compliance‑related issues.
Collaborate with manufacturing teams to ensure successful scale‑up of formulations from laboratory to production scale. Provide technical support during manufacturing to troubleshoot any formulation‑related challenges.
Conduct alternate supplier qualification of existing raw materials. Design experiments to evaluate stability and suitability of alternate material in new and existing finished products. Conduct sensory analysis for raw materials where needed to ensure suitability of flavors and other ingredients in powder products.
Maintain accurate and detailed records of formulation development activities, experiments, and results. Generate technical reports, protocols, and documentation as needed.
Work closely with cross‑functional teams including Sales, Project Management, Product Development, Quality Control, Regulatory Affairs, Quality Assurance, and Technical Operations to ensure alignment with project goals and timelines.
Stay updated with the latest developments in formulation science and technological advancements in the dietary supplement industry. Incorporate innovative approaches and ingredients into formulation strategies.
Adhere to laboratory safety protocols and follow Good Laboratory Practices (GLP) to ensure a safe and compliant working environment.
Identify opportunities for increased efficiency.
Perform additional duties as assigned.
May supervise the activity of junior staff in the department.
Skills Formulation, nutraceutical, GLP, chemistry, supplement formulation, nutrition formulation, dietary supplement, powder, capsule, stability testing, vitamin, FDA, allergen.
Qualifications
Bachelor's degree in a relevant scientific field (e.g., pharmaceutical sciences, chemistry, biology) with at least 3 years of experience in nutraceutical, food, pharmaceutical or similar industries.
Advanced degrees (MS or PhD) preferred.
Strong experience in nutraceutical/pharmaceutical formulation/process development (capsules, powders, tablets, DTM powders, effervescent tablets, and powders) and related laboratory techniques.
Demonstrated success in formulating, scaling up and commercializing complex formulations.
Knowledge of FDA regulations around dietary supplements, cGMP, and DSHEA guidelines.
Proven experience in conducting scientific research, designing experiments, analyzing data with statistical tools, and providing detailed reports.
Proficiency in using laboratory equipment relevant to product development.
Root‑cause analysis and troubleshooting formulation issues.
Experience with Product Lifecycle Management Software is preferred.
Excellent communication and collaboration skills for working within cross‑functional team environments, especially with manufacturing, operations, sales, and quality.
Experience working in a fast‑paced environment with multiple priorities.
Pay & Benefits Pay range: $52.00 – $61.00/hr. Application deadline: Dec 31, 2025.
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan – Pre‑tax and Roth post‑tax contributions available
Life Insurance (Voluntary Life & AD&D for employee and dependents)
Short‑ and long‑term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, vacation or sick leave)
Workplace type: Fully onsite in Valencia, CA.
About Actalent Actalent is a global leader in engineering and science services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Actalent is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email
actalentaccommodation@actalentservices.com
for other accommodation options.
#J-18808-Ljbffr
Valencia, CA Employment Type:
Full‑time, Permanent Seniority Level:
Mid‑Senior
The Research and Development Senior Formulation Scientist plays a critical role in the selection of ingredients, development and optimization of formulations for dietary supplements and food products. This position involves proper assessment of active and non‑active ingredients, experimental design, scientific judgement and the application of scientific principles to create high‑quality, stable, and efficacious product formulations that meet the outlined product profile.
Responsibilities
Selection of appropriate ingredients, development of paper formulations and reformulations that meet product profiles and development objectives.
Perform benchtop experiments for development of nutraceutical products (capsules, tablets, powders, stick packs), considering client requirements, manufacturing feasibility, ingredient compatibility, stability, solubility, and bioavailability.
Evaluate and select appropriate excipients and recommend alternate active ingredients for use in formulations based on scientific understanding and regulatory requirements.
Reformulate products to enhance appearance, taste, texture, solubility, stability, efficacy, and manufacturability with speed, accuracy and robustness.
Ensure that formulated products meet quality standards, regulatory guidelines, and industry best practices. Collaborate with regulatory and quality teams to address and resolve any compliance‑related issues.
Collaborate with manufacturing teams to ensure successful scale‑up of formulations from laboratory to production scale. Provide technical support during manufacturing to troubleshoot any formulation‑related challenges.
Conduct alternate supplier qualification of existing raw materials. Design experiments to evaluate stability and suitability of alternate material in new and existing finished products. Conduct sensory analysis for raw materials where needed to ensure suitability of flavors and other ingredients in powder products.
Maintain accurate and detailed records of formulation development activities, experiments, and results. Generate technical reports, protocols, and documentation as needed.
Work closely with cross‑functional teams including Sales, Project Management, Product Development, Quality Control, Regulatory Affairs, Quality Assurance, and Technical Operations to ensure alignment with project goals and timelines.
Stay updated with the latest developments in formulation science and technological advancements in the dietary supplement industry. Incorporate innovative approaches and ingredients into formulation strategies.
Adhere to laboratory safety protocols and follow Good Laboratory Practices (GLP) to ensure a safe and compliant working environment.
Identify opportunities for increased efficiency.
Perform additional duties as assigned.
May supervise the activity of junior staff in the department.
Skills Formulation, nutraceutical, GLP, chemistry, supplement formulation, nutrition formulation, dietary supplement, powder, capsule, stability testing, vitamin, FDA, allergen.
Qualifications
Bachelor's degree in a relevant scientific field (e.g., pharmaceutical sciences, chemistry, biology) with at least 3 years of experience in nutraceutical, food, pharmaceutical or similar industries.
Advanced degrees (MS or PhD) preferred.
Strong experience in nutraceutical/pharmaceutical formulation/process development (capsules, powders, tablets, DTM powders, effervescent tablets, and powders) and related laboratory techniques.
Demonstrated success in formulating, scaling up and commercializing complex formulations.
Knowledge of FDA regulations around dietary supplements, cGMP, and DSHEA guidelines.
Proven experience in conducting scientific research, designing experiments, analyzing data with statistical tools, and providing detailed reports.
Proficiency in using laboratory equipment relevant to product development.
Root‑cause analysis and troubleshooting formulation issues.
Experience with Product Lifecycle Management Software is preferred.
Excellent communication and collaboration skills for working within cross‑functional team environments, especially with manufacturing, operations, sales, and quality.
Experience working in a fast‑paced environment with multiple priorities.
Pay & Benefits Pay range: $52.00 – $61.00/hr. Application deadline: Dec 31, 2025.
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan – Pre‑tax and Roth post‑tax contributions available
Life Insurance (Voluntary Life & AD&D for employee and dependents)
Short‑ and long‑term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, vacation or sick leave)
Workplace type: Fully onsite in Valencia, CA.
About Actalent Actalent is a global leader in engineering and science services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Actalent is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email
actalentaccommodation@actalentservices.com
for other accommodation options.
#J-18808-Ljbffr