Full-Time

Quality Control Supervisor

Posted on 8/21/2026

Englewood Lab

Englewood Lab

Compensation Overview

$65k - $75k/yr

+ Discretionary bonus

Totowa, NJ, USA

In Person

Bachelor's

Category
QA & Testing (1)
Required Skills
ERP
Quality Assurance (QA)
OSHA
Data Analysis
Requirements
  • A minimum of a Diploma or Bachelor degree in Life Sciences, Engineering, or a related profession.
  • At least five years of industry or related experience in cosmetics, medical devices, food, or pharmaceuticals.
  • Previous inspecting, auditing, or manufacturing experience is beneficial.
  • Data analysis and specification development skills.
  • Computer literacy and effective communication skills.
Responsibilities
  • Schedule Quality Control Inspectors for bulk manufacturing, production or assembly lines, warehouse finished-goods auditing, special sample handling, and review of in-process records and related documentation.
  • Conduct nonconformance, product complaint, and out-of-specification investigations, and provide corrective and preventive actions with follow-up.
  • Train and supervise document review personnel, batch release personnel, Quality Control Leads, Inspectors, and Associates.
  • Issue certificates of conformance, certificates of manufacture, and certificates of analysis to customers for finished goods.
  • Maintain accurate records of approved, quarantined, and rejected products within specified areas.
  • Ensure compliance with standard operating procedures and regulatory requirements, including FDA, EPA, OSHA, and ISO 13485:2003.
  • Review finished goods with the shipping department for formal release and compliance with customer requirements.
  • Work closely with the Quality Assurance and Quality Systems departments on quality and compliance matters.
  • Maintain working knowledge of inspection requirements for components, raw materials, in-process or bulk materials, and finished goods.
  • Ensure that Quality Control Inspectors review in-process manufacturing and production or assembly activities for conformance to specifications and follow up on nonconformances and out-of-specifications.
  • Participate in in-process quality training programs.
  • Conduct periodic analysis of the in-process inspection program and make recommendations.
  • Assist in interpreting or developing customer specifications and assembly or packaging requirements.
  • Assist in establishing production and assembly inspection information sheets and required documentation.
  • Maintain and update the enterprise resource planning system and repositories of batch records, documents, and manufacturing and assembly specifications.
  • Review batch records, worksheets, inspection documentation, Quality Control inspection reports, and production or in-process information for completeness and correctness.
  • Facilitate on-site customer inspections by coordinating product availability and communicating dispositions to Quality and Inventory Control.
  • Interface with customer distribution operations when needed.
  • Maintain compliance with safety regulations while performing job duties.
  • Ensure that finished goods, bulk materials, raw materials, and components are maintained correctly in warehouses and other holding areas.
  • Assist with the review and release of finished products.
  • Perform supplier and vendor audits, mock recalls, and internal audits.
  • Perform additional duties or assignments as directed by the supervisor.

Company Size

N/A

Company Stage

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Total Funding

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Headquarters

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Founded

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