JBAndrews
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.
Position – QC Analytical Chemist Position Overview
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.
Key Responsibilities
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.
Qualifications and Expertise
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.
Additional Requirements
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.
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Research
Industries Food and Beverage Manufacturing and Pharmaceutical Manufacturing
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Position – QC Analytical Chemist Position Overview
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.
Key Responsibilities
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.
Qualifications and Expertise
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.
Additional Requirements
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.
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Research
Industries Food and Beverage Manufacturing and Pharmaceutical Manufacturing
#J-18808-Ljbffr