Quality Control Technician

Responsibilities

• Work in a clean room manufacturing environment to support the production of biological medical devices derived from porcine liver.
• Receive porcine livers and verify materials according to established procedures.
• Trim porcine livers and prepare tissue samples for further processing.
• Scoop, measure, and mix chemical solutions used in liver processing, following precise instructions and safety guidelines.
• Create, cut, and prepare specific tissue pieces for use in medical devices, ensuring accuracy and consistency.
• Sterilize and maintain the cleanliness of the clean room, including equipment and work surfaces, to meet sterile processing standards.
• Follow SOPs and work instructions rigorously to ensure compliance with GMP and regulatory requirements.
• During non-build weeks, perform assembly tasks related to device production and component preparation.
• Sweep floors, clean work areas, and perform general housekeeping duties in the clean room and surrounding spaces as needed.
• Update manufacturing records (MFR paperwork) and maintain accurate documentation of production activities.
• Support administrative tasks such as order receiving and shipping-related activities as needed.
• Collaborate with the R&D team and other technicians to support production and development activities.
• Work directly with porcine livers during production cycles and assist R&D with porcine kidneys during downtime.
• Maintain strong attention to detail in all aspects of work, including tissue handling, chemical mixing, documentation, and cleaning.
• Adhere to safety protocols, aseptic techniques, and sterile processing practices to protect product quality and personal safety.
• Contribute to a small, collaborative team environment and work independently when required to meet production timelines.

Requirements

• Minimum of 6+ months of experience working within a clean room setting.
• Associate degree in a medical or science-related field.
• Experience following SOPs in a GMP-regulated environment.
• Demonstrated strong attention to detail, verified through references or prior work experience.
• Hands-on experience with cleanroom practices and sterile processing.
• Knowledge of aseptic technique and sterilization procedures.
• Ability to safely mix and handle chemicals used in biological processing.
• Comfort working on feet for the majority of the day and lifting 5–15 pound bins and tissue materials.
• Capability to maintain accurate manufacturing documentation and follow regulated processes.

Qualifications

• Associate degree in a scientific field, such as biology, is preferred.

Skills

• Strong attention to detail.
• Knowledge of aseptic technique and sterilization procedures.
• Ability to safely mix and handle chemicals used in biological processing.
• Comfort working on feet for the majority of the day and lifting 5–15 pound bins and tissue materials.
• Ability to maintain accurate manufacturing documentation and follow regulated processes.

Benefits

• Medical, dental & vision coverage.
• Critical Illness, Accident, and Hospital coverage.
• Life Insurance (Voluntary Life & AD&D for the employee and dependents).
• Short and long-term disability coverage.
• Health Spending Account (HSA).
• Transportation benefits.
• Employee Assistance Program.
• Time Off/Leave (PTO, Vacation or Sick Leave).

Pay and Benefits

The pay range for this position is $21.00 - $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 coverage.
• Critical Illness, Accident, and Hospital coverage.
• Life Insurance (Voluntary Life & AD&D for the employee and dependents).
• Short and long-term disability coverage.
• Health Spending Account (HSA).
• Transportation benefits.
• Employee Assistance Program.
• Time Off/Leave (PTO, Vacation or Sick Leave).

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 actalentaccommodation@actalentservices.com for other accommodation options.