QA Lab Technician

Ethicon, a member of the Johnson & Johnson Family of Companies, is recruiting for a QA Lab Technician located in its manufacturing site at San Lorenzo, Puerto Rico.

Ethicon, part of the Johnson & Johnson Medical Devices Companies, has made significant contributions to surgery for more than 60 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures. Our continuing dedication to Shape the Future of Surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives. Through Ethicon's surgical technologies and solutions including sutures, staplers, energy devices, trocars and hemostats and our commitment to treat serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact. For more information, visit www.ethicon.com .

Thriving on a diverse company culture, celebrating the uniqueness of our employees, and committed to inclusion. Proud to be an equal opportunity employer.

Under the direction of the Quality Supervisor, Laboratory, or designee, and with the objective of maintaining high Quality Laboratory Practice and compliance with regulatory requirements, performs chemical and physical analysis of raw materials, in process and finished products. Collect environmental samples according to established procedures.

Responsibilities:

• Performed and evaluate required laboratory test on raw materials, in-process, and finish good materials as per applicable procedures. Also, perform environmental monitoring (viable for surface and air).

• Ensure correct and complete documentation of all tests performed, laboratory logbook, and calibrations verifications.

• Complete all record retention documentation.

• Confirm the proper inventory of laboratory supplies, environmental monitoring materials, and reagents are available to perform laboratory test / monitoring activities.

• Document and evaluate results of product endotoxin, bioburden, and sterility test.

• Keep records following GDP and GMP.

• Maintain work areas and equipment clean and audit ready according to applicable procedures.

• Reports any Out of Specification (OOS) condition, escalate, and document / completed the investigation according to established procedures and assuring its completion following the laboratory investigation report timeframe.

• Coordinates on time calibration of QA laboratory equipment.

• Collect waste, segregate where required and store in designated areas as per applicable procedures.