Actalent
Quality Control Laboratory Technician
As a Quality Control Laboratory Technician, you will be responsible for using micrometers and calipers to measure incoming instruments and ensure they meet the required standards. You will review drawings and instruments to verify product accuracy, report on part conditions and non-conformances, and ensure custom OEM orders meet customer specifications. You will update QMS systems and paper documents as needed for audits, and utilize Good Manufacturing Practices (GMP) throughout all processes. Responsibilities
Receive and unpack incoming shipments; verify quantities and assess the condition of materials. Perform inspections on raw materials and finished goods using technical drawings and specifications, including dimensional checks, functional testing, and visual assessments. Record inspection outcomes in quality systems, complete necessary documentation, and flag any non-conforming items. Apply product identification markings using laser or chemical etching methods; clean and neutralize items as needed. Handle product returns and customer complaints by evaluating quality concerns and coordinating necessary repairs or rework. Support regulatory compliance efforts by preparing documentation and maintaining relevant databases. Follow all applicable quality and safety standards, including industry-specific regulations and internal procedures. Maintain cleanliness and organization in the quality control area. Monitor inventory of quality-related supplies and request replenishments as needed. Provide training on inspection procedures and assist with onboarding new team members. Uphold the organization's quality objectives and contribute to continuous improvement efforts. Perform additional tasks and responsibilities as assigned. Essential Skills
Experience with inspection tools such as calipers and micrometers. Quality Assurance experience, preferably in medical devices, though experience in pharmaceuticals is also considered. Familiarity with Good Manufacturing Practices (GMP). Ability to read and interpret drawings and specifications. High attention to detail. Additional Skills & Qualifications
High School diploma or equivalent is required. Experience in Quality Control or Quality Assurance is preferred. Work Environment
The standard schedule is Monday through Friday with flexible start times between 6:30 AM and 9:00 AM, and shifts typically end by 6:00 PM. You will collaborate closely with fellow inspectors and cross-functional team members in a shared inspection area, where strong teamwork and attention to detail are essential. Reporting to the Quality Manager, you'll work within a team that includes quality and operations supervisors, engineers, and inspectors. The position operates in the quality department alongside shipping, receiving, labeling, and laser marking personnel, totaling 810 team members. The role is best suited for candidates located near Emerson for a manageable commute of no more than 45 minutes. Pay and Benefits
The pay range for this position is $24.00 - $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 Emerson, NJ. Application Deadline
This position is anticipated to close on Aug 26, 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, please email actALENTaccommodation@actalentservices.com for other accommodation options.
As a Quality Control Laboratory Technician, you will be responsible for using micrometers and calipers to measure incoming instruments and ensure they meet the required standards. You will review drawings and instruments to verify product accuracy, report on part conditions and non-conformances, and ensure custom OEM orders meet customer specifications. You will update QMS systems and paper documents as needed for audits, and utilize Good Manufacturing Practices (GMP) throughout all processes. Responsibilities
Receive and unpack incoming shipments; verify quantities and assess the condition of materials. Perform inspections on raw materials and finished goods using technical drawings and specifications, including dimensional checks, functional testing, and visual assessments. Record inspection outcomes in quality systems, complete necessary documentation, and flag any non-conforming items. Apply product identification markings using laser or chemical etching methods; clean and neutralize items as needed. Handle product returns and customer complaints by evaluating quality concerns and coordinating necessary repairs or rework. Support regulatory compliance efforts by preparing documentation and maintaining relevant databases. Follow all applicable quality and safety standards, including industry-specific regulations and internal procedures. Maintain cleanliness and organization in the quality control area. Monitor inventory of quality-related supplies and request replenishments as needed. Provide training on inspection procedures and assist with onboarding new team members. Uphold the organization's quality objectives and contribute to continuous improvement efforts. Perform additional tasks and responsibilities as assigned. Essential Skills
Experience with inspection tools such as calipers and micrometers. Quality Assurance experience, preferably in medical devices, though experience in pharmaceuticals is also considered. Familiarity with Good Manufacturing Practices (GMP). Ability to read and interpret drawings and specifications. High attention to detail. Additional Skills & Qualifications
High School diploma or equivalent is required. Experience in Quality Control or Quality Assurance is preferred. Work Environment
The standard schedule is Monday through Friday with flexible start times between 6:30 AM and 9:00 AM, and shifts typically end by 6:00 PM. You will collaborate closely with fellow inspectors and cross-functional team members in a shared inspection area, where strong teamwork and attention to detail are essential. Reporting to the Quality Manager, you'll work within a team that includes quality and operations supervisors, engineers, and inspectors. The position operates in the quality department alongside shipping, receiving, labeling, and laser marking personnel, totaling 810 team members. The role is best suited for candidates located near Emerson for a manageable commute of no more than 45 minutes. Pay and Benefits
The pay range for this position is $24.00 - $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 Emerson, NJ. Application Deadline
This position is anticipated to close on Aug 26, 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, please email actALENTaccommodation@actalentservices.com for other accommodation options.