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Job Description

We are looking for a Quality Assurance Inspector to join our team and ensure that all production activities meet the highest standards of quality and compliance. This role is critical in maintaining adherence to Good Manufacturing Practices (GMPs) and company policies while supporting continuous improvement initiatives.

Key Responsibilities:

+ Perform daily inspections of all production lines to verify compliance with GMPs and company standards.

+ Accurately document inspection details on Daily Inspection Reports (DIR), including lot numbers, item numbers, fill weights, defects, and other required data.

+ Confirm that all manufacturing specifications for components, labeling, and products are correct and complete.

+ Conduct line clearance inspections to ensure removal of previous products and readiness of work areas.

+ Monitor, sample, and inspect in-process products for quality; perform tests and collect data to support product disposition.

+ Determine and apply appropriate disposition labels to inspected materials.

+ Identify and report discrepancies from procedures or specifications to Production and Quality teams.

+ Perform AQL inspections and execute rework protocols as needed.

+ Initiate and log samples in LIMS; retain samples per SOPs.

+ Print specifications from ERP systems, create shop order packages, and distribute to Production.

+ Collect and ship samples for customers, stability programs, and validations as required.

+ Review documentation for accuracy prior to QA release and verify Master Batch Sheets.

+ Act as Lead QA Inspector when needed to ensure proper coverage of production lines.

+ Support trials, validations, and continuous improvement initiatives.

+ Perform testing as outlined in SOPs and Work Instructions.

Required Skills

+ Quality Assurance and Quality Control

+ GMP compliance

+ Inspection and documentation accuracy

+ Familiarity with AQL standards and sampling plans

Additional Qualifications

+ Associate’s Degree in a scientific, technical, or related field (or equivalent experience).

+ Minimum 3+ years in a regulated industry (FDA, EPA, ISO), preferably in manufacturing or QA.

+ Strong understanding of GMPs, quality systems, and regulated environments.

+ Experience with batch documentation, component verification, and in-process inspections.

+ Proficiency in Microsoft Office and ability to learn systems like LIMS and ERP.

+ Excellent attention to detail, organizational skills, and ability to multitask.

+ Effective communication and collaboration skills across teams.

+ Ability to interpret SOPs, Work Instructions, and Master Batch Records.

+ Leadership skills to act as QA lead when required.

Job Type & Location

This is a Contract to Hire position based out of Wharton, NJ.

Pay and Benefits

The pay range for this position is $20.00 - $25.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Wharton,NJ.

Application Deadline

This position is anticipated to close on Dec 29, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.