Quality Control Chemist

JBAndrews; New York (NY); On-site; USD 80,000 - 100,000; Full time

Job summary

A reputable Nutraceutical manufacturing company in New York is seeking a QC Analytical Chemist to oversee quality control testing and method development. This full-time, onsite position requires a Bachelor's degree and over 5 years of experience in the dietary supplements industry. Responsibilities include analytical testing, ensuring compliance with regulatory standards, and producing high-quality documentation. Join a respected team committed to product integrity and continuous improvement.

Qualifications

• More than 5 years’ experience in a QC lab within the dietary supplements industry.
• Hands-on experience with various analytical equipment.
• Strong knowledge of Quality Control and Regulatory Affairs.

Responsibilities

• Perform analytical testing on raw materials and finished products.
• Develop and validate analytical methods; write detailed documentation.
• Ensure compliance with GLP, cGMP, and regulatory requirements.

Skills

Analytical testing

Documentation skills

Compliance with cGMP

Problem-solving skills

Interpersonal communication

Education

Bachelor's degree

Tools

HPLC

GC

UV FTIR

FTNIR

ICP-MS

Job description

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