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Description

The Associate Formulation Scientist will support the development of innovative dietary supplement products. The successful candidate will assist in the formulation, testing, and documentation of dietary supplements/nutritional products including tablets, capsules, powders. This role involves collaboration with cross-functional teams including R&D team, Quality, Regulatory, Procurement and Manufacturing. This position is responsible for the hands-on evaluation of the raw materials, bench development of formulations of different dosage forms, and conducting appropriate chemical and physical laboratory tests to ensure ingredients and formulations meet the target product profile. Responsibilities Assist in the design and development of new products, and reformulation of products by translating customer requirements and specifications into finished product that meet product profile and can be manufactured at target cost. Conduct bench-top prototype development, laboratory experiments and testing according to established protocols and procedures. This may involve sample preparation, formulation, stability testing, sensory evaluation (in-house or third party) and submitting samples for analytical testing. Perform ingredient sourcing, functionality evaluation, and compatibility studies. Conduct laboratory experiments and testing according to established protocols and procedures. This may involve sample preparation, formulation, stability testing, sensory evaluation (in-house or third party) and submitting samples for analytical testing. Assist with evaluation of new/alternate raw materials for use in finished products. Communicate with manufacturing, production, quality and packaging to resolve quality related issues with production lots. Support scale-up and pilot production trials in coordination with manufacturing teams. Record experimental data accurately and analyze results. Use statistical tools and software to draw meaningful conclusions. Leverage existing data to draw conclusion and manage risk. Maintain detailed laboratory notebooks and records. Generate technical reports summarizing findings and progress in product development. Maintain records on testing and develop and maintain forms as needed. Prepare technical transfer reports, SOP’s and work instructions as needed. Stay current with industry regulations and standards related to dietary supplements and nutritional products. Work closely with Quality department to ensure formulations align with labeling / regulatory requirements. Collaborate with cross-functional teams, including product development, quality assurance, regulatory affairs, sales and manufacturing, to deliver product development milestones against timeline and budget and ensure product development aligns with company goals and standards. Conduct literature research to support formulation design and market research to support innovative ingredient and product solutions. Using research, design formulations to deliver quality products and use existing data and historical records to continuously improve existing products. Comply with safety protocols and standard operating procedures (SOPs) in the laboratory. Promote a culture of safety among team members. Operate, clean, and maintain laboratory equipment and instruments. Work with R&D technician to report any malfunctions or need for repairs. Additional Duties as assigned

Skills

Formulation, product development, R&d, supplement, vitamin, food, GMP, GLP, laboratory, FDA, deitary

Top Skills Details

Formulation,product development,R&d

Additional Skills & Qualifications

Bachelor's degree in a relevant scientific field (e.g., chemistry, biology, food science, or related discipline). or equivalent combination of education and relevant experience. Master's degree in a related scientific field, preferred Experience: 1-3+ years of experience working in an R&D or product development laboratory, preferably in the pharmaceutical, dietary supplement, or food industry. Strong knowledge of laboratory techniques, equipment, and safety protocols. Familiarity with formulation development, experimental design, and analytical testing. Proficient in using laboratory software and data analysis tools. Knowledge of functional ingredients such as vitamins, minerals, botanicals, amino acids, probiotics, etc. Familiarity with different dosage forms and delivery systems (e.g., tablets, capsules, powders). Familiarity with nutritional value calculation and product labeling regulations and guidelines. Ability to follow protocols and standard operating procedures accurately and safely. Adherence to quality standards and commitment to maintaining a safe laboratory environment. Knowledge of GMP (Good Manufacturing Practices) and GLP (Good Lab Practices) guidelines. Experience with setting up stability protocols and conducting stability testing Familiarity with FDA regulations for dietary supplements / raw materials.

Experience Level

Intermediate Level

Job Type & Location

This is a Contract position based out of Valencia, CA.

Pay and Benefits

The pay range for this position is $22.00 - $40.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• 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 the 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

This is a fully onsite position in Valencia,CA.

Application Deadline

This position is anticipated to close on Dec 16, 2025.

About Actalent

Actalent is a global leader in engineering and sciences 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.

The company 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 [email protected] (%[email protected]) for other accommodation options.