- Integra LifeSciences (Plainsboro, NJ)
- …all duties in accordance to the requirements of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other ... as assigned. **DESIRED MINIMUM QUALIFICATIONS** The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.… more
- Integra LifeSciences (Plainsboro, NJ)
- …activities such as training, investigations, procedure development, and inventory management within the manufacturing area. Drive a positive culture within ... needs and support recover plan development and execution. + Partner with area management to identify overtime needs in advance. + Communicate with support groups on… more
- Integra LifeSciences (Plainsboro, NJ)
- …activities such as training, investigations, procedure development, and inventory management within the manufacturing area. Drive a positive culture within ... needs and support recover plan development and execution. + Partner with area management to identify overtime needs in advance. + Communicate with support groups on… more
- Fujifilm (Edison, NJ)
- …sharing technical insights, service trend data, and field failures with Product Management , Engineering, and Sales teams. + Represent post-sale service in global ... and implement retention strategies to sustain organizational health and continuity. Financial Management & Vendor Oversight + Manage the full departmental budget and… more
- Integra LifeSciences (Plainsboro, NJ)
- …activities such as training, investigations, procedure development, and inventory management within the manufacturing area. Drive a positive culture within ... needs and support recover plan development and execution. * Partner with area management to identify overtime needs in advance. * Communicate with support groups on… more
- Integra LifeSciences (Plainsboro, NJ)
- …and cGMP environments. The qualified candidate must understand the concepts of risk management and the ability to identify and classify critical parameters within a ... all projects are in compliance with cGMP, cGLP, QSR (including Design Controls), ISO or other applicable requirements. + Support and address comments and suggestions… more
- Integra LifeSciences (Plainsboro, NJ)
- …and mentoring to Product Release group members and provides support to management . Directs, coordinates, and evaluates the activities of associates in the Product ... procedures. Must have working knowledge of US Food and Drug Administration regulations, ISO 9001, ISO 13485, the European Medical Device Directive, Canadian… more
- Integra LifeSciences (Plainsboro, NJ)
- …compliance with all company policies and procedures and appropriate regulations, including FDA and ISO 9001, ISO 13485, CMDR and the Medical Device Directive. + ... with OSHA and Standard Operating Procedures. + Demonstrate organizational and time management skills. + Perform other related duties as required. DESIRED MINIMUM… more
- ARUNDEL MACHINE (Emerson, NJ)
- …and maintain regulatory databases + Adhere strictly to all CGMP, FDA 21 CFR820, ISO 13485, EU MDR and company procedures to ensure the quality and integrity of ... each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations… more
- WM (Trenton, NJ)
- …expected travel 20-35% of time **I. Job Summary** This is a project management position involving the development, design and delivery of organics recycling and ... The ideal candidate will possess superior problem solving and management skills that will be applied to a diverse...state and industry standards and codes, such as ASME, ISO and related electrical controls and classifications to ensure… more