- Sun Pharmaceuticals, Inc (Princeton, NJ)
- …branded market with a focus on dermatology, ophthalmology and onco-dermatology. **Job Summary:** As a ** QA Medical Device Specialist II** , you will ... the QA Head in ensuring that all medical devices and combination productswhether manufactured in-house or by...related field. + **24 years** of experience in a medical device or pharmaceutical manufacturing environment. +… more
- Sun Pharmaceuticals, Inc (Princeton, NJ)
- …pharmaceutical and medical device products. This role provides Quality Assurance support across manufacturing operations, including batch record review, ... market with a focus on dermatology, ophthalmology and onco-dermatology. **Job Summary:** The QA Specialist II is responsible for ensuring compliance with Current… more
- Terumo Medical Corporation (Somerset, NJ)
- …forwarding of customer complaints (eg, adverse events, product performance reports, etc.) to Quality Assurance ( QA ), and by ensuring all promotional ... develops, manufactures, and markets a complete, solutions-based portfolio of high- quality medical devices used in a broad...of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in… more
- Terumo Medical Corporation (Somerset, NJ)
- …of product, recognizing customer complaints and the requirement to forward information to Quality Assurance + Offer ideas, methods, or processes for improvement ... Field Inventory Specialist Date: Oct 23, 2025 Req ID: 4839...inventory redistribution amongst multiple field-based inventory locations in the medical device or pharmaceutical space strongly preferred.… more
- Terumo Medical Corporation (Somerset, NJ)
- Sr. Clinical Quality Specialist Date: Oct 21, 2025 Req ID: 5279 Location: Somerset, NJ, US Company: Terumo Medical Corporation Department: Clinical Affairs ... develops, manufactures, and markets a complete, solutions-based portfolio of high- quality medical devices used in a broad...of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in… more
- Integra LifeSciences (Princeton, NJ)
- …Operating Procedures + Strong understanding of supply chain principles, quality assurance processes, and regulatory requirements in the medical device ... collaborating closely with cross-functional teams to support our mission of delivering high- quality medical devices. Under the direction of the Director, Direct… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …your best self. Become a **maker of possible** with us. The Site Supplier Quality Specialist is responsible for defining and executing the supplier management ... and working with other functions in the organization including Quality Engineering, WW Supplier Quality Assurance...other related discipline + At least 3-5 years of medical device , biologic, pharmaceutical, or diagnostic industry… more
- Cardinal Health (Trenton, NJ)
- …certification is a plus. + 2-4 years of experience in data governance, quality assurance , or regulatory compliance role within the medical device or a ... (FDA) and the European Union under the EU 2017/745 Medical Device Regulation (EU MDR) and meets...the regulatory department and other functions, such as R&D, Quality Assurance , Marketing and Legal, to ensure… more
- Pentax Medical (Montvale, NJ)
- …Opening: Senior Regulatory Affairs Specialist Why JOIN Us? We are an established medical device leader that is preparing for high growth. This means that ... play a crucial role in shaping the future of medical technology. Responsibilities of Senior Regulatory Affairs Specialist...review meetings. + Work in partnership with manufacturing and QA /QC in designing and enhancing quality management… more
- Integra LifeSciences (Plainsboro, NJ)
- …US. Food and Drug Administration Regulations, ISO 9001, ISO 13485:2016 Standard, European Medical Device Directives, Canadian Medical Device Regulations, ... patient outcomes and set new standards of care. The ** Quality Compliance Specialist ** will provide quality...perform each essential duty satisfactorily. + Review and approve quality documents requiring QA oversight (eg, IOPQ… more
