Actalent
Quality Assurance Technician (Overnight Shift Sun–Thurs)
In this role you will perform daily inspections of all production lines to ensure compliance with Good Manufacturing Practices (GMPs) and company standards. Accurately document all inspection details including incoming lot numbers, liquid lot numbers, item numbers, fill weights, and defects. Ensure manufacturing specifications for components, labeling, and products are correct, clear, and complete. Inspect work areas for removal of all previous products and components and verify readiness prior to use.
Responsibilities
Monitor, sample, and inspect in‑process finished products for quality by performing appropriate tests.
Collect data and samples to support the disposition of products.
Determine final disposition of inspected products and verify information on transfer tickets.
Apply appropriate disposition labels to materials.
Identify and notify Production and Quality teams when discrepancies from procedures and specifications are observed.
Perform AQL inspections as required.
Execute rework protocols as needed.
Initiate and log LIMS and retain samples.
Print specifications from ERP systems, create shop order packages, and provide them to Production as needed.
Collect samples required by customers or PDI specifications and ship samples accordingly.
Collect stability samples.
Execute trials and validations.
Review documentation for accuracy before submitting to the QA Release team.
Review Master Batch Records and act as Lead QA Inspector in their absence.
Identify continuous improvement opportunities and promote a culture of quality.
Handle assignments to establish and maintain product quality.
Perform required testing as per SOPs and WIs.
Essential Skills
Quality assurance and inspection experience.
Minimum 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, sampling plans, and in‑process quality control methods.
Familiarity with batch documentation, manufacturing specifications, and component/label verification.
Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
Ability to learn and operate quality‑related systems such as LIMS, ERP, and electronic documentation tools.
Demonstrated experience performing in‑process quality inspections, line clearances, material disposition, and documentation review.
Experience supporting trials, validations, rework activities, and sample collection.
Prior exposure to continuous improvement, deviation identification, and collaboration with Production/Quality teams.
Strong ability to interpret and follow SOPs, Work Instructions, Master Batch Records, and product specifications.
Excellent documentation accuracy, attention to detail, and commitment to “first‑time‑right” execution.
Effective communication skills with the ability to escalations discrepancies and collaborate across teams.
Solid organizational, multitasking, and time‑management skills.
Additional Skills & Qualifications
Associate’s Degree in a scientific, technical, or related field, or equivalent combination of education and experience.
Ability to take initiative and identify improvement opportunities.
Excellent organizational and leadership skills.
Job Type & Location Permanent position based out of Orangeburg, NY.
Pay And Benefits The pay range for this position is $55,000.00 – $60,000.00 per year.
Benefits include:
Medical & Prescription benefits
Dental and vision insurance
Life insurance
Health Savings Account
Flexible Spending Account
Disability Insurance
EAP/Health Advocate
Auto & Homeowners insurance
Pet Insurance
Tuition Reimbursement
401k + match
Workplace Type Fully onsite position in Orangeburg, NY.
Application Deadline This position is anticipated to close on Jan 2, 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.
Seniority Level
Mid‑Senior level
Employment Type
Full‑time
Job Function
Quality Assurance
Industries
Business Consulting and Services
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Responsibilities
Monitor, sample, and inspect in‑process finished products for quality by performing appropriate tests.
Collect data and samples to support the disposition of products.
Determine final disposition of inspected products and verify information on transfer tickets.
Apply appropriate disposition labels to materials.
Identify and notify Production and Quality teams when discrepancies from procedures and specifications are observed.
Perform AQL inspections as required.
Execute rework protocols as needed.
Initiate and log LIMS and retain samples.
Print specifications from ERP systems, create shop order packages, and provide them to Production as needed.
Collect samples required by customers or PDI specifications and ship samples accordingly.
Collect stability samples.
Execute trials and validations.
Review documentation for accuracy before submitting to the QA Release team.
Review Master Batch Records and act as Lead QA Inspector in their absence.
Identify continuous improvement opportunities and promote a culture of quality.
Handle assignments to establish and maintain product quality.
Perform required testing as per SOPs and WIs.
Essential Skills
Quality assurance and inspection experience.
Minimum 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, sampling plans, and in‑process quality control methods.
Familiarity with batch documentation, manufacturing specifications, and component/label verification.
Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
Ability to learn and operate quality‑related systems such as LIMS, ERP, and electronic documentation tools.
Demonstrated experience performing in‑process quality inspections, line clearances, material disposition, and documentation review.
Experience supporting trials, validations, rework activities, and sample collection.
Prior exposure to continuous improvement, deviation identification, and collaboration with Production/Quality teams.
Strong ability to interpret and follow SOPs, Work Instructions, Master Batch Records, and product specifications.
Excellent documentation accuracy, attention to detail, and commitment to “first‑time‑right” execution.
Effective communication skills with the ability to escalations discrepancies and collaborate across teams.
Solid organizational, multitasking, and time‑management skills.
Additional Skills & Qualifications
Associate’s Degree in a scientific, technical, or related field, or equivalent combination of education and experience.
Ability to take initiative and identify improvement opportunities.
Excellent organizational and leadership skills.
Job Type & Location Permanent position based out of Orangeburg, NY.
Pay And Benefits The pay range for this position is $55,000.00 – $60,000.00 per year.
Benefits include:
Medical & Prescription benefits
Dental and vision insurance
Life insurance
Health Savings Account
Flexible Spending Account
Disability Insurance
EAP/Health Advocate
Auto & Homeowners insurance
Pet Insurance
Tuition Reimbursement
401k + match
Workplace Type Fully onsite position in Orangeburg, NY.
Application Deadline This position is anticipated to close on Jan 2, 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.
Seniority Level
Mid‑Senior level
Employment Type
Full‑time
Job Function
Quality Assurance
Industries
Business Consulting and Services
#J-18808-Ljbffr