Job Title: Quality Assurance Technician

Book if interested: https://talentassistant.actalentservices.com/assistant/bookings/BfUTMTxl

Must have QA experience within GMP environment

Job Description

As a Quality Assurance Technician, you will perform daily inspections of all production lines to ensure compliance with Good Manufacturing Practices (GMPs) and company standards. You will document inspection information accurately on the Daily Inspection Report (DIR) and ensure all manufacturing specifications are correct and complete. Your role will involve inspecting work areas, monitoring in-process finished products, collecting data and samples, and determining final product disposition.

Responsibilities

Perform daily inspections of production lines to ensure GMP compliance.Document all inspection details including lot numbers, fill weights, and defects.Ensure manufacturing specifications for components, labeling, and products are correct.Inspect work areas for removal of previous products and verify readiness.Monitor, sample, and inspect finished products for quality through appropriate tests.Collect data and samples to support product disposition decisions.Determine and verify final product disposition and apply disposition labels.Identify and report discrepancies to Production and Quality teams.Perform AQL inspections and execute Rework protocols as needed.Initiate and log LIMS and Retain Samples, and print specifications from ERP systems.Collect and ship samples as required by customers or Manufacturing Instructions.Collect stability samples and execute Trials and Validations.Review documentation for accuracy prior to submission to QA Release team.Act as Lead QA Inspector in absence, ensuring proper production floor coverage.Identify continuous improvement opportunities and promote a culture of quality.Conduct any required testing as per SOPs and Work Instructions.

Essential Skills

3+ years of quality experience in a regulated environment.Strong understanding of GMPs, quality systems, and regulated manufacturing environments.Working knowledge of AQL inspection standards and in-process quality control methods.Familiarity with batch documentation and manufacturing specifications.Proficiency in Microsoft Office Suite and ability to learn quality-related systems.Experience with in-process quality inspections, line clearances, and documentation review.Experience supporting trials, validations, rework activities, and sample collection.Ability to interpret and follow SOPs, Work Instructions, and product specifications.Excellent documentation accuracy and attention to detail.Effective communication skills and ability to collaborate across teams.

Additional Skills & Qualifications

Associate’s Degree in a scientific, technical, or related field, or equivalent experience.Experience in a regulated industry (e.g., FDA, EPA), preferably in manufacturing or QA roles.Prior exposure to continuous improvement and deviation identification.Solid organizational, multitasking, and time-management skills.Ability to take initiative and support a quality-focused culture.

Work Environment

The position is for the 2nd shift, Monday to Friday from 3pm to 11:30pm, with overtime required on Saturdays as needed.

Job Type & Location

This is a Permanent position based out of Orangeburg, NY.

Pay and Benefits

The pay range for this position is $55000.00 - $60000.00/yr.

MedicalDentalVisionAccidental/Life401k + matchHolidays, Vacation & Sick Time

Workplace Type

This is a fully onsite position in Orangeburg,NY.

Application Deadline

This position is anticipated to close on Feb 13, 2026.

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 actalentaccommodation@actalentservices.com for other accommodation options.