QA Inspector

Actalent; Bohemia (NY); On-site; USD 33,000 - 40,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Paid time off

Job summary

Actalent is seeking a QA Inspector to join our clinical label manufacturing team in Bohemia, NY. You will perform visual and automated inspections at multiple stages, ensuring labels meet specifications and regulatory standards.

The role requires documenting results and reporting trends to supervision. Ideal candidates have at least 1 year in QA/QC in a cGMP setting, experience with automated inspection equipment, and a keen eye for detail.

Qualifications

• Minimum 1 year of QA/QC experience in a regulated environment.
• Experience in a cGMP environment is required.
• Strong attention to detail and accuracy in inspections.
• Proficient in documenting inspection results and records.
• Troubleshooting skills for inspection processes.
• Ability to work in a fast-paced, team-oriented manufacturing environment.
• High school diploma or equivalent.

Responsibilities

• Perform visual and automated quality inspections at multiple stages throughout the manufacturing process.
• Inspect pharmaceutical labels for accuracy, legibility, alignment, print quality, and regulatory compliance.
• Set up, monitor, and perform routine checks on automatic inspection equipment.
• Identify defects, non-conformities, and deviations from specifications in labels and production materials.
• Document inspection results clearly and accurately, and maintain complete and organized quality records.
• Report quality issues, inspection findings, and trends promptly to supervision or management.
• Troubleshoot inspection issues and assist in identifying root causes and corrective actions.
• Maintain production pace while ensuring quality standards and regulatory requirements are met.

Tools

Automated inspection equipment

Job description

QA Inspector

The QA/QC Inspector performs in-process and finished goods inspections within a clinical label manufacturing environment. This role focuses on inspecting labels and production materials, identifying and documenting quality issues, and ensuring that all products meet established quality and regulatory requirements.

Responsibilities

• Perform visual and automated quality inspections at multiple stages throughout the manufacturing process.

• Inspect pharmaceutical labels for accuracy, legibility, alignment, print quality, and overall compliance with specifications and regulatory requirements.

• Set up, monitor, and perform routine checks on automatic inspection equipment to ensure proper operation.

• Identify defects, non-conformities, and deviations from specifications in labels and production materials.

• Document inspection results clearly and accurately, and maintain complete and organized quality records.

• Report quality issues, inspection findings, and trends promptly to supervision or management.

• Troubleshoot inspection issues and assist in identifying root causes and implementing corrective actions.

• Maintain production pace while consistently ensuring that quality standards and regulatory requirements are met.

Essential Skills

• Minimum 1 year of experience in quality assurance (QA), quality control (QC), or a closely related field.

• Experience working in a cGMP (current Good Manufacturing Practice) environment.

• Experience with automated inspection equipment in a manufacturing or packaging setting.

• Strong attention to detail and accuracy in visual and automated inspections.

• Proficiency in documenting inspection results and maintaining quality records.

• Troubleshooting and problem-solving skills related to inspection processes and equipment.

• Ability to work effectively in a fast-paced, team-oriented manufacturing environment.

• High school diploma or equivalent.

Additional Skills & Qualifications

• Experience with pharmaceutical or clinical label review.

• Quality assurance, quality control, or quality inspection within a manufacturing environment.

• Familiarity with batch record review and documentation practices.

• Comfort performing overnight work on a consistent schedule.

Work Environment

This role is based in a clinical label manufacturing facility that operates on a 3rd shift schedule from 11:00 PM to 7:30 AM.

The environment is fast-paced and team-oriented, with a strong focus on compliance with cGMP standards and quality control procedures. The QA/QC Inspector works closely with production teams and uses both visual methods and automated inspection equipment to evaluate labels and materials. The position requires sustained attention to detail, consistent documentation, and the ability to maintain productivity while upholding strict quality and regulatory standards.

Job Type & Location

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

Pay and Benefits

The pay range for this position is $24.00 - $29.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

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)

Job Type & Location

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

Application Deadline

This position is anticipated to close on Nov 17, 2026.

Workplace Type

This is a fully onsite position in Bohemia,NY.

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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.