• Integra LifeSciences Corporation
  • $100,590.00 -160,840.00/year*
  • Union , NJ
  • Scientific Research
  • Full-Time
  • 3 Bond Dr

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 4,500 employees worldwide. Integra's common stock is listed on The NASDAQ Stock Market under the symbol \"IART.\" Ensure compliance with all company policies and procedures and appropriate regulations, including FDA and ISO 9001, ISO 13485, CMDR and the Medical Device Directive Perform and document instrumental (i.e., UV-Vis, HPLC) and wet chemistry techniques/analyses Perform laboratory testing, as well as general laboratory maintenance, including in process and final product release testing and stability testing Ensure timely testing and result reporting Submit samples for shipment to third party labs when necessary Maintain GMP/GLP laboratory notebooks and documentation relevant to the duties and responsibilities assigned Maintain laboratory instrumentation required for testing Assist as needed in test method validation, implementation, and execution Report any equipment and testing deviations to the Supervisor Assist with proper execution of laboratory Out-of-Specification (OOS) investigations Complete data entry for trending reports for In-process and Finished Goods Quality Control Testing, as well as Stability Testing Train team members in Analytical department as assigned Handle and dispose of biohazard material in compliance with OSHA and Standard Operating Procedures Demonstrate organizational and time management skills Perform other related duties required Basic requirements Bachelor's degree in chemistry, biological science or closely related discipline 0-2+ years of experience, preferably in a quality control laboratory Understanding and practice of GMP and GLP Experience with MS Office Suite Preferred requirements Ability to effectively communicate both written and verbal information Ability to work independently under minimal supervision, commensurate with experience level Experience closely following prescribed processes High attention to detail to the exclusion of errors Desire to raise up technical and procedural better practices Willingness to work occasional over-time or off-shift hours
Associated topics: chemical engineering, coatings, nutrition, pha, phenolic, plastics, polymer, polymer synthesis, polypropylene, polyurethane

* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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