Quality Control Chemist

I am currently partnered with a Nutraceutical contract manufacturing company based in Long Island, New York. This is an onsite position, 5 days a week full time. Looking to onboard ASAP. This is an excellent opportunity to grow with a reputable and highly respected company within the Nutraceutical Industry.

• Experienced Chemist role within the dietary supplements industry.
• Responsible for Quality Control testing, method development, and compliance with cGMP standards.
• Ensures product integrity through accurate analysis and documentation.

• Perform analytical testing on raw materials, in-process materials, and finished products.
• Develop, validate, and transfer analytical methods; write detailed method documentation.
• Implement and maintain laboratory SOPs.
• Interpret data independently and produce high-quality reports.
• Ensure compliance with GLP, cGMP, and regulatory requirements.
• Stay current with evolving regulatory standards and industry best practices.

• Bachelor’s degree with more than 5 years’ experience in a QC lab within the dietary supplements industry.
• Hands‑on experience with analytical equipment: HPLC, GC, UV FTIR, FTNIR, ICP‑MS.
• Strong knowledge of Quality Control, GLP, and Regulatory Affairs.
• Understanding of product specifications, allergen statements, and MSDS.
• Experience handling dietary supplement ingredients, in-process materials, and finished products.
• Ability to work independently, solve problems, and enforce compliance with cGMP.
• Excellent documentation skills and interpersonal communication.
• Proven ability to thrive in a fast‑paced, multidisciplinary team environment.

• Ability to produce high‑quality documentation of work.
• Maintain awareness of current regulatory requirements for dietary supplement labeling and claims.
• Strong leadership skills to ensure subordinates follow cGMP standards.

Mid‑Senior level

Full‑time

Research

Food and Beverage Manufacturing and Pharmaceutical Manufacturing