QA Lab Technician

Job Description This role focuses on inspecting, measuring, and documenting the quality of instruments and medical devices to ensure they meet strict customer, regulatory, and internal specifications. The Quality Assurance Inspector plays a key part in supporting patient safety by maintaining high quality standards, updating quality systems, and collaborating with teams to resolve non-conformances and quality concerns. Job Title: Quality Assurance Technician Job Description This role focuses on inspecting, measuring, and documenting the quality of instruments and medical devices to ensure they meet strict customer, regulatory, and internal specifications. The Quality Assurance Inspector plays a key part in supporting patient safety by maintaining high quality standards, updating quality systems, and collaborating with teams to resolve non-conformances and quality concerns. Responsibilities Inspect incoming instruments and components using micrometers, calipers, and other measurement tools to verify they meet required specifications. Review engineering drawings and physical instruments to confirm that products match documented requirements and customer expectations. Evaluate customer drawings for custom OEM orders and ensure all products conform to specified dimensions, tolerances, and quality standards. Report on the condition of parts, identifying and documenting non-conformances and any items that are out of specification (OOS). Record inspection outcomes in quality systems, complete all necessary documentation, and promptly flag non-conforming items for further action. Update the Quality Management System (QMS) and paper-based documents as needed to support audits and maintain accurate quality records. Apply product identification markings using laser or chemical etching methods, and clean and neutralize items as required to ensure safe handling. Handle product returns and customer complaints by assessing quality concerns, documenting findings, and coordinating repairs or rework as appropriate. Support regulatory compliance activities by preparing documentation, maintaining relevant databases, and following applicable regulations and internal procedures. Utilize Good Manufacturing Practices (GMP) in daily work to maintain consistent, high-quality production and inspection standards. Follow all applicable quality and safety standards, including industry-specific regulations and internal quality procedures. Maintain cleanliness and organization in the quality control area to support safe, efficient, and compliant operations. Monitor inventory of quality-related supplies, such as gauges and consumables, and request replenishment when levels are low. Collaborate with quality assurance and operations team members to resolve quality issues and continuously improve inspection processes. Essential Skills Quality assurance and inspection experience, preferably in a medical device environment, with openness to candidates from other regulated industries. Hands-on experience using micrometers and calipers to measure and verify product dimensions. Strong familiarity with Good Manufacturing Practices (GMP) and quality control processes. Ability to read and interpret technical drawings, blueprints, and specifications with a high degree of accuracy. Great attention to detail and accuracy when inspecting parts, reviewing documentation, and recording quality data. Understanding of regulatory and quality frameworks such as ISO 13485, FDA 21 CFR 820, and EU MDR. High school diploma or equivalent education. Ability to document inspection results clearly and completely in both electronic quality systems and paper records. Capability to identify non-conforming items and communicate issues effectively to the appropriate stakeholders. Additional Skills & Qualifications Prior quality assurance experience specifically within the medical device sector is preferred. Familiarity with laboratory or controlled environment practices related to inspection and testing. Experience working within a formal Quality Management System (QMS) and supporting internal or external audits. Comfort working with product identification methods such as laser marking and chemical etching. Ability to manage product returns and customer complaints with a focus on root cause analysis and corrective actions. Strong organizational skills to maintain orderly documentation, workspaces, and inventory of quality tools and supplies. Team-oriented mindset with the ability to collaborate closely with quality assurance and operations teams. Interest in contributing to a mission-driven organization focused on helping patients and improving healthcare outcomes. Work Environment The role is based in a small, close-knit organization with a team-oriented, family-style culture. The quality assurance team consists of approximately five people, working closely with an operations team of four to five colleagues. The standard schedule is Monday through Friday, with flexible start times between 6:30 AM and 9:00 AM and shifts typically ending by 6:00 PM, offering some flexibility to accommodate personal needs. The workspace is undergoing remodeling, providing an updated and improved environment. The company offers a 12-month contract-to-hire structure, with eligibility for quarterly bonuses once converted to permanent status. Benefits begin on the first day of permanent employment, and a 401(k) plan starts at 90 days, complemented by three weeks of paid time off for permanent employees. The work centers on helping patients through high-quality medical products, and employees use standard quality inspection tools such as micrometers, calipers, and laser or chemical etching equipment in a clean, organized quality control area. Job Type & Location This is a Contract to Hire position based out of Emerson, NJ. Pay And Benefits The pay range for this position is $24.00 - $25.00/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) Workplace Type This is a fully onsite position in Emerson,NJ. Application Deadline This position is anticipated to close on Oct 16, 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 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 View email address on click.appcast.io 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. #J-18808-Ljbffr Actalent