Integra LifeSciences, a world leader in medical technology, is dedicated to limiting uncertainty for surgeons, so they can concentrate on providing the best patient care. Integra offers innovative solutions in orthopedic extremity surgery, neurosurgery, reconstructive and general surgery, and regenerative wound care.
Integra's orthopedic products include devices and implants for foot and ankle, hand and wrist, shoulder and elbow, tendon and peripheral nerve protection and repair. Integra is a leader in neurosurgery, offering a broad portfolio of implants, devices, instruments and systems used in neurosurgery, neuromonitoring, neurotrauma, and related critical care. Integra’s Tissue Technologies is an in-patient and outpatient Regenerative product portfolio, which includes products for wound care, burns, abdominal reconstruction, and plastic & reconstructive surgery. In the United States, Integra is a leading provider of surgical instruments to hospitals, surgery centers and alternate care sites, including physician and dental offices.
Founded in 1989 Integra is headquartered in Plainsboro, New Jersey and has over 3,300 employees worldwide. Integra's common stock is listed on The NASDAQ Stock Market under the symbol "IART."
(1)Co-ordinates and performs in-process and final product inspection at the designated China sites in accordance with established procedures.
(2)Compiles and reviews batch record documentation which includes sterilization records, USP testing records and production inspection records
(3)Ensures timely retrieval and review of all quality records and forwards all records in a timely manner to the QA/QC Manager for review
(4)Responsible to promote good manufacturing practices and quality awareness among the production staff at the designated China sites
(5)Co-ordinates with the QA/QC Manager in a timely investigation of customer complaints, non-conformances and follow-up on any corrective actions
(6)Ensures no changes are facilitated at the suppliers location without prior approval from the QA/QC Manager
(7)Facilitates transfer of raw material specifications to the manufacturing sites and ensure only the most updated documents are present
(8)Participates in weekly meeting with the QA/QC Manager
(9)Performs additional duties as required
(1)Minimum a College degree or diploma in the science field or related work experience
(2)Knowledge of ISO Quality Standards, GMP
(3)Communicating and writing skills in English a must
(4)Compute knowledge is required