Changing lives. Building Careers. Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging whatâs possible and making headway to help improve outcomes. ⢠Ensures that adequate Quality support is provided to productions and to open projects / initiatives ç¡®ä¿ä¸ºç产å项ç®/计åæä¾è¶³å¤çè´¨éæ¯æ ⢠Ensures that Nonconformances are initiated, dispositioned, approved and investigated according to plans and in compliance with procedures and regulatory requirements ç¡®ä¿ä¸ç¬¦åæç
§è®¡åãç¨åºåæ³è§è¦æ±è¿è¡å¯å¨ãå¤çãè°æ¥åæ¹å ⢠Ensures that quality activities for validation of new processes/ products are performed and documented according to procedures and within the defined timeline ç¡®ä¿æ°å·¥èº/产åéªè¯çè´¨éæ´»å¨æç
§ç¨åºå¹¶å¨è§å®çæ¶é´å
è¿è¡å¹¶è®°å½ ⢠Write protocols and reports for validation documentation (such as process validation, test method validation, validation plan.) ç¼åéªè¯ææ¡£çæ¹æ¡åæ¥å(å¦å·¥èºéªè¯ï¼æµè¯æ¹æ³éªè¯ï¼éªè¯è®¡åç) ⢠Ensures that risk analysis activities (PFMEA) are performed and documented according to procedures and within the defined timeline ç¡®ä¿é£é©åææ´»å¨(PFMEA)å¨è§å®çæ¶é´å
æç
§ç¨åºè¿è¡å¹¶è®°å½ ⢠Organize meeting for risk analysis activities and write risk management documentation ç»ç»é£é©åæä¼è®®ï¼æ°åé£é©ç®¡çæä»¶ ⢠Ensures that GMP rules are known, understood, and respected on the site ç¡®ä¿GMPè§åå¨ç°åºè¢«äºè§£ãçè§£åéµå® ⢠Ensure technical support to QC and laboratory department ç¡®ä¿QCåå®éªå®¤é¨é¨çææ¯æ¯æ ⢠Collaborate with supplier quality team, manage supplier, ensure suppliers are qualified based on procedures to meet regulation requirements. åä¾åºåè´¨éå¢éåä½ï¼ç®¡çä¾åºåï¼ç¡®ä¿ä¾åºå被è¯ä¼°åå®¡æ ¸ï¼æ»¡è¶³æ³è§è¦æ± ⢠Escalates quality issues and makes sure that appropriate actions are in place to fix the issue in a compliant manner å级质éé®é¢ï¼å¹¶ç¡®ä¿éåéå½çæªæ½ä»¥åè§çæ¹å¼è§£å³é®é¢ ⢠Participates and supports internal and third-party audits / inspections åä¸å¹¶æ¯æå
é¨åç¬¬ä¸æ¹å®¡æ ¸/æ£æ¥ ⢠Manages or participates to quality projects 管çæåä¸è´¨éé¡¹ç® â¢ Provides support to complaint investigation 为æè¯è°æ¥æä¾æ¯æ ⢠Establish product related quality system documents, participate to procedure elaboration or update 建ç«å产åç¸å
³çä½ç³»æä»¶ï¼å䏿µç¨çç»åææ´æ° â¢ Establish testing method for products, ensure applicable gages or equipment for products testing, train inspectors and ensure inspectors can understand the testing method. 建ç«äº§åçæµè¯æ¹æ³ï¼ç¡®ä¿äº§åæ£æµæåéçéå
·å设å¤ï¼å¯¹æ£éªåè¿è¡å¹è®ï¼ç¡®ä¿æ£éªåè½ææ¡æµè¯æ¹æ³ ⢠Ensure that the release of raw materials and semi-finished products complies with procedures and regulatory requirement ç¡®ä¿åææååæåçæ¾è¡ç¬¦åç¨åºåæ³è§è¦æ± ⢠Ensure that the release of finished products complies with the requirements of procedures and regulations ç¡®ä¿æåçæ¾è¡ç¬¦åç¨åºåæ³è§çè¦æ± ⢠Ensures that CAPA are managed and documented according to plans and in compliance with procedures ç¡®ä¿CAPAæç
§è®¡ååç¨åºè¿è¡ç®¡çåè®°å½ â¢ Ensure all quality system related change are initiated, evaluated, and ensure all actions of change control are followed up closely and closed in time. ç¡®ä¿å½±åè´¨éä½ç³»çç¸å
³åæ´è½æç
§æä»¶è¦æ±åèµ·ï¼è¯ä¼°ï¼å¹¶ç¡®ä¿åæ´ç¸å
³çæ´»å¨å¯ä»¥åæ¶å®æ ⢠Ensures support to process improvement projects ç¡®ä¿å¯¹å·¥èºæ¹è¿é¡¹ç®çæ¯æ ⢠Arrange the daily work of the inspectors, provide necessary training, ensure that the inspectors meet the qualification requirements for their positions. Complete other tasks assigned by the supervisor. 宿æ£éªåæ¥å¸¸å·¥ä½ï¼æä¾å¿
è¦çå¹è®ï¼ç¡®ä¿æ£éªå符åå²ä½èµè´¨è¦æ±ãå®æä¸»ç®¡å®æçå
¶ä»ä»»å¡ã Unsolicited Agency Submission Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidateâs name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails. Changing Lives. Building Careers. 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 neurosurgery, reconstructive and general surgery, and regenerative wound care. Founded in 1989 Integra is headquartered in Princeton, New Jersey and has more than 4,000 employees worldwide. Integraâs common stock is listed on The NASDAQ Stock Market under the symbol âIART.â