Actalent
Description
Inspect incoming raw materials pertaining to Disposables and Electronics. Inspect finished products. Document all non-conformances when necessary. Assist with investigations pertaining to both customer complaints and internal non-conformances. Understand, follow, and practice the rules and regulations set forth by the QSR, ISO 13485 and the company’s internal guidelines.
Requirements
High School graduate or equivalent work-related experiences with some previous quality control experience desired (minimum of 5 years)
Strong inspection ability using a caliper, micrometer, vision system including optical comparator, OGP Smart system, and other inspection and measurement tools
Detail oriented, computer literate and possesses a professional demeanor, be adaptable to changing environments and capable of completing tasks with little or no supervision
Computer skills including MS Excel and MS Access (basic knowledge of each)
Good written and oral communication skills are required and must be able to read, write, and understand English
Interpersonal skills dealing with other departments/individuals in a team atmosphere important
Ability to read and interpret engineering drawings, product specifications, and procedures and use metrology and other testing equipment
Medical device experience desired
Skills Quality control, Troubleshooting, caliper, micrometer, inspection, QC, Pneumatics, Mechanical, electrical testing
Duties
Review processes to assure procedural compliance and recommend improvements
Perform and review visual, dimensional and functional inspection of incoming raw materials pertaining to Disposables and Electronics. Ability to identify key inspection points and the proper tools/equipment to ascertain these points
Perform inspections and verification of finished products
Review inspection data and DHRs (including sterilization records) for accuracy and compliance to the applicable standards
Perform inspections and process Returned goods/materials (RGAs/RMAs)
Use recognized sampling plans to determine statistical size of samples
Perform and review tests according to various GMP protocol requirements
Document and review inspection results per GMP/GDP
Generate non-conforming material reports (NCMR) for products that do not conform to test specifications and contact the appropriate personnel
Communicate needs of department/company to management
Assist engineering staff with process improvement projects regarding improved quality inspection of product and components (such as First Article Inspections and qualification testing)
Ability to work in all QA areas (IQC, Finals and Electronics) if needed
Execute and maintain 5S environment
Experience Level Intermediate Level
Pay and Benefits The pay range for this position is $20.50 – $21.00/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 Allen,TX.
Application Deadline This position is anticipated to close on Oct 31, 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, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.
Actalent
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Requirements
High School graduate or equivalent work-related experiences with some previous quality control experience desired (minimum of 5 years)
Strong inspection ability using a caliper, micrometer, vision system including optical comparator, OGP Smart system, and other inspection and measurement tools
Detail oriented, computer literate and possesses a professional demeanor, be adaptable to changing environments and capable of completing tasks with little or no supervision
Computer skills including MS Excel and MS Access (basic knowledge of each)
Good written and oral communication skills are required and must be able to read, write, and understand English
Interpersonal skills dealing with other departments/individuals in a team atmosphere important
Ability to read and interpret engineering drawings, product specifications, and procedures and use metrology and other testing equipment
Medical device experience desired
Skills Quality control, Troubleshooting, caliper, micrometer, inspection, QC, Pneumatics, Mechanical, electrical testing
Duties
Review processes to assure procedural compliance and recommend improvements
Perform and review visual, dimensional and functional inspection of incoming raw materials pertaining to Disposables and Electronics. Ability to identify key inspection points and the proper tools/equipment to ascertain these points
Perform inspections and verification of finished products
Review inspection data and DHRs (including sterilization records) for accuracy and compliance to the applicable standards
Perform inspections and process Returned goods/materials (RGAs/RMAs)
Use recognized sampling plans to determine statistical size of samples
Perform and review tests according to various GMP protocol requirements
Document and review inspection results per GMP/GDP
Generate non-conforming material reports (NCMR) for products that do not conform to test specifications and contact the appropriate personnel
Communicate needs of department/company to management
Assist engineering staff with process improvement projects regarding improved quality inspection of product and components (such as First Article Inspections and qualification testing)
Ability to work in all QA areas (IQC, Finals and Electronics) if needed
Execute and maintain 5S environment
Experience Level Intermediate Level
Pay and Benefits The pay range for this position is $20.50 – $21.00/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 Allen,TX.
Application Deadline This position is anticipated to close on Oct 31, 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, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.
Actalent
#J-18808-Ljbffr