- Bausch + Lomb (Trenton, NJ)
- …the life cycle to interdisciplinary project teams and to appropriate management level in Regulatory Affairs , R&D, TechOps and Supply Chain as appropriate in a ... company functions during Regulatory Authority inspections. + Serve as Regulatory Affairs representative on facility/site Local Change Management Boards. +… more
- Bausch + Lomb (Bridgewater, NJ)
- …* Bachelor's degree preferred or equivalent. * Minimum of 8 years in Regulatory Affairs with experience in the consumer product (Rx/OTC, OTC Monograph, ... business acumen and ability to see the business drivers outside of Regulatory Affairs . * Ability to influence internal and external key stakeholders and KOL.… more
- Bausch + Lomb (Bridgewater, NJ)
- …transfers and geographical expansion projects on behalf of the Global Regulatory Affairs department. **Responsibilities** * Responsible for general knowledge ... Bachelor degree preferred or equivalent * Minimum 1.5 years of Regulatory Affairs Project management experience * PMP Certification preferred Specific Skills: *… more
- Integra LifeSciences (Princeton, NJ)
- …are challenging what's possible and making headway to help improve outcomes. The Regulatory Affairs Specialist is responsible for implementing regulatory ... with all current and upcoming regulations in the US and EU. The Regulatory Affairs Specialist is responsible for providing regulatory input for… more
- Bausch + Lomb (Bridgewater, NJ)
- …to meet regulations. + Leads meetings and discussions with cross-functional teams ( Regulatory Affairs , Medical Affairs , Engineering, Quality, Legal, ... as assigned. **Requirements** **TECHNICAL COMPETENCIES:** Knowledge of medical device regulatory affairs discipline throughout the product lifecycle including… more
- Novo Nordisk (Plainsboro, NJ)
- …oversight and decision-making. Coordinate cross-functional collaboration among commercial teams, medical affairs , regulatory affairs , and other stakeholders ... in? Are you ready to experiment with us? The Position The Portfolio Operations Specialist will play a pivotal role in overseeing the Novo Nordisk's product portfolio… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …mgmt. and incorporate them into the change management process. + Collaborate with Regulatory Affairs and Quality Assurance teams to ensure that all necessary ... of quality management systems, change control processes, and GMP/GDP regulatory requirements. + Familiarity with conducting quality assessments and implementing… more
- Gentiva (Piscataway, NJ)
- …and compliance required + Registered Nurse required, BSN preferred + Strong regulatory affairs and governance requirements for healthcare + Thorough knowledge ... day. **Overview** We are looking for an **Executive Director Specialist RN** that will travel to many of our...of state and local guidelines that govern regulatory processes for healthcare + Able to travel 100%… more
- Hovione (East Windsor, NJ)
- …- Training and experience of GMP standards (mandatory) - Experience of working with Regulatory Affairs and a well-rounded knowledge of the function (mandatory) - ... IOPs are up to date, compliant and supports efficient production - Review regulatory documentation and co-ordination of site documentation to support regulatory … more
- Pacific Northwest National Laboratory (Trenton, NJ)
- …including unmanned aerial systems (UAS). This includes legal and regulatory frameworks, identification and interdiction of threat materials, physical security, ... an ability to understand the complexity of different cultures and foreign affairs . **Hazardous Working Conditions/Environment** + The position may be subject to… more
- Terumo Medical Corporation (Somerset, NJ)
- …NJ, US, 08873 Company: Terumo Medical Corporation Department: Medical Affairs Operations Terumo Medical Corporation (TMC) develops, manufactures, and markets ... and implementing the clinical advisory vision and strategy in alignment with Medical Affairs and the organization. This role will develop and manage a highly… more
- Hackensack Meridian Health (Edison, NJ)
- …+ Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... compliant study conduct according to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures. This role carries… more