Quality Manager/Document Control Specialist; Bilingual in EN & Chinese
Job in
Port Washington, Nassau County, New York, 11050, USA
Listed on 2026-03-11
Listing for:
The Voluntary Protection Programs Participants' Association, Inc
Full Time
position Listed on 2026-03-11
Job specializations:
-
Quality Assurance - QA/QC
Quality Control / Manager, Quality Technician/ Inspector -
Manufacturing / Production
Job Description & How to Apply Below
Location: Port Washington
America's Best Nutrition, a contract manufacturer of nutritional products and dietary supplements has an opening for a new position,
Quality Manager/Document Control Specialist. Located in Long Island, NY, our company has grown significantly through exceptional channel relationships, product innovation, and the reputation of its brands for potency, quality, and value.
- Managing all aspects of our quality and GMP operation.
- Identifying and establishing finished product specifications and release criteria for product components and finished products.
- Establishing and developing the company's SOP system, document control system, product specifications, and all other documentation systems required by regulations
- Managing our 3rd-party contract lab partnerships for inbound and finished product testing requirements.
- Reviewing and releasing all product batch records for raw materials, labels, packaging materials, and finished products
- Assisting in supervising and coordinating QA, QC, and production employees' all activities in all aspects of product development from raw materials to finished products for dietary supplements
- Performing routine training activities and inspections to assure all employees and the entire plant adherence to cGMP.
- Reviewing and closing investigations for customer complaints, production discrepancies, and OOS, initiating and implementing CAPA if needed
- Monitor and continuously improve the Quality system by evaluating supporting documentation to ensure compliance to cGMP, Industry standards, and other applicable regulations
- Perform routine inspections of equipment and facilities to ensure required manufacturing in-process controls are implemented
- Lead case-based teams to investigate production discrepancy when needed
- Some lab work including microbial testing, physical testing and other parameters as needed
Bachelor's degree or above in QA/QC and FDA Regulatory affairs, or other relevant degrees.
Knowledge of the following:CFR 21 Section 111, Food and/or dietary supplement manufacturing GMPs, Testing experience with FT-IR, ICP, Microbial Petrifilm and Disintegrations test are preferred.
Prefer:Bilingual in English and Chinese
Job Type: Full-time
Pay: $55,000.00 - $80,000.00 per year
Work Location:
In person
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