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QA Specialist- Dietary Supplement

Job in Edgewood, Greene County, New York, USA
Listing for: The Voluntary Protection Programs Participants' Association, Inc
Full Time position
Listed on 2026-05-26
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 26.81 - 42.29 USD Hourly USD 26.81 42.29 HOUR
Job Description & How to Apply Below
Location: Edgewood

Position Summary

We are seeking a Quality Assurance (QA) Specialist with dedicated experience to oversee the compliance, safety, and physical integrity of our dietary supplement lines. This role focuses heavily on shop-floor quality operations, Master Batch Record verification, and in-process controls specifically tailored to automated tablet compression presses and high-speed capsule filling machines.

Key Responsibilities
  • In-Process Controls
    :
    Perform routine floor audits and verify in-process checks during manufacturing, including tablet hardness, thickness, friability, weight variation, and capsule fill weights.
  • Equipment Verification
    :
    Review and approve machine setup, clearance protocols, and cleaning validation logs (swab/rinse testing) for tablet presses and capsule fillers to prevent cross-contamination.
  • Batch Record Review
    :
    Audit executed batch records, encapsulation logs, and tablet compression run charts for accuracy, yield calculations, and compliance with 21 CFR Part 111.
  • Deviation & OOS Investigation
    :
    Lead investigations into machine-related deviations, such as tablet capping/lamination, weight fluctuations, or capsule defects, and implement effective CAPA plans.
  • SOP Maintenance
    :
    Draft and update Standard Operating Procedures (SOPs) for the operation, sanitation, and quality verification of solid-dose production equipment.
Qualifications & Technical Requirements
  • Education
    :
    Bachelor’s degree in chemistry, Biology, Food Science, Chemical Engineering, or a related technical discipline.
  • Industry Experience
    :
    Minimum 2–4 years of QA or high-level Quality Control experience inside a cGMP dietary supplement or pharmaceutical facility.
  • Machinery Knowledge
    :
    Hands‑on familiarity with the operational quality parameters of automated tablet compression tooling and semi‑automatic or fully automatic capsule filling equipment.
  • Regulatory Expertise
    :
    Strong working knowledge of FDA dietary supplement regulations (21 CFR Part 111).

Pay: $26.81 - $42.29 per hour

Work Location:

In person

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