- Integra LifeSciences (Princeton, NJ)
- … regulatory compliance, and cost management/process efficiency objectives. The Labeling Associate will collaborate with cross-functional teams, including ... patient outcomes and set new standards of care. The Labeling Associate will assist with the execution...ensuring compliance with both internal corporate standards and external regulatory requirements. This role will be assisting the strategic… more
- Integra LifeSciences (Princeton, NJ)
- …pathways to advance patient outcomes and set new standards of care. The Labeling Associate - Design is responsible for creating, reviewing, approving, and ... members for and project teams on all project execution + Assist the Senior Labeling Associate in integrating and implementing Integra's electronic labeling … more
- Takeda Pharmaceuticals (Trenton, NJ)
- …application is true to the best of my knowledge. **Job Description** The Regulatory Affairs- Labeling , Associate Director is responsible for ensuring that ... to the world. **How you will contribute:** + The Associate Director, GRA Labeling Compliance, is responsible...strategic and operational activities pertaining to global and local labeling compliance and quality within Global Regulatory … more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director, Global Labeling Lead where you will be responsible for ... of labeling documentation and assures that Takeda labeling content and processes conform to regulatory ...Takeda labeling content and processes conform to regulatory requirements. Management of Local Exceptions and LOC Interactions… more
- Ascendis Pharma (Princeton, NJ)
- …committed to working together as one team to achieve extraordinary results. The Associate Director Regulatory Affairs, Advertising and Promotion will be an ... the promotion of prescription drug and biologic products. The Associate Director Regulatory Affairs, Advertising and Promotion... impact of new campaign concepts, target, or product labeling , and to provide strategic regulatory guidance… more
- Sumitomo Pharma (Trenton, NJ)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs** . The Associate Director is ... the US. He/she will primarily function as a Regional Regulatory Leader (RRL) and is responsible for ensuring the...support the successful submission and achievement of target product labeling + Accountable in conjunction with the GRL for… more
- Bristol Myers Squibb (Princeton, NJ)
- …. **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion ... pharmaceutical products across therapeutic areas + Responsible for understanding the regulatory landscape, assessing regulatory risk, and developing global… more
- Bristol Myers Squibb (Princeton, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Position: Associate Director, WW Medical Neuropsychiatry Strategy, Schizophrenia** **Location: ... Princeton Pike or Madison, NJ** The Associate Director of Medical Strategy, Schizophrenia will partner with key medical team to support development, implement, and… more
- Merck (West Point, PA)
- …colleagues across our enterprise. We are seeking a highly experienced and knowledgeable Associate Director of Electrical Power Systems to join our team. The ideal ... testing program, Safe Electrical Work Practices Site Procedure, Arc Flash Analysis/ Labeling ). Act as a technical resource for hazardous work involving electricity.… more
- Integra LifeSciences (Plainsboro, NJ)
- …to advance patient outcomes and set new standards of care. The warehouse Associate / Manufacturing operator will verify and keep records of all incoming and outgoing ... inventory locations, and perform all associated transactions in ORACLE. The warehouse associate will perform all required duties in compliance with company policies,… more
- Catalent Pharma Solutions (Philadelphia, PA)
- …for Clinical Supply Packaging. Catalent offers GMP secondary packaging and clinical labeling services throughout our global network. Packaging can be configured to ... over dry ice depending upon your project needs. Using our Clinicopia global labeling system with its multi-lingual label phrase library we can design single panel,… more
- J&J Family of Companies (Spring House, PA)
- …Support development strategy, study design and protocols for clinical trials that support regulatory submissions and product labeling + Engage in clinical trial ... best practices in data management to enable system level software designs Regulatory Affairs Associate : + Conducting a research project on a topic impacting the … more
- Catalent Pharma Solutions (Philadelphia, PA)
- …for Clinical Supply Packaging. Catalent offers GMP secondary packaging and clinical labeling services throughout our global network. Packaging can be configured to ... depending upon your project needs. Using our Clinicopia global labeling system with its multi-lingual label phrase library we...and assessments of problems or potential problems to the Associate Director, QMS + Lead the implementation of new… more
- Endo International (Horsham, PA)
- …Works with all levels of management and suppliers to accomplish all regulatory compliance objectives. Trains junior QA team members. Batch Record/Reports Review + ... to preparation and/or review of annual product review and updates for regulatory filing(s), batch release metrics, and department reporting as applicable. + Releases… more
- Integra LifeSciences (Plainsboro, NJ)
- …in ensuring that products meet the required safety, performance, and regulatory standards before they reach the market. Their responsibilities typically include: ... visual, mechanical, and sometimes functional tests to ensure products meet regulatory requirements (such as FDA or ISO standards). Documentation and Reporting:… more
- Fujifilm (Trenton, NJ)
- …leading laboratories across the country and diagnostic chemicals for OEM white labeling products. The company is headquartered in Lexington, Massachusetts. For more ... healthcare professionals, sales & field personnel, global R&D, operations, regulatory , global marketing, infection control, other companies/device manufacturers, etc.)… more
- Fujifilm (Trenton, NJ)
- …leading laboratories across the country and diagnostic chemicals for OEM white labeling products. The company is headquartered in Lexington, Massachusetts. For more ... all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements, and all other applicable… more
- Fujifilm (Trenton, NJ)
- …leading laboratories across the country and diagnostic chemicals for OEM white labeling products. The company is headquartered in Lexington, Massachusetts. For more ... all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable… more
- Integra LifeSciences (Plainsboro, NJ)
- …ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to be familiar with and able to measure critical ... test records. * Perform line clearances and quality reviews in manufacturing, labeling , or other assigned areas during manufacturing activities. * Identify and… more