- Takeda Pharmaceuticals (Cambridge, MA)
- …to patients worldwide. Join Takeda as an Associate Director, Global Reg Affairs Device , PDT in our Global Regulatory Affairs CMC & Device organization ... Affairs CMC & Device organization is responsible for global device regulatory strategies and activities for the PDT BU product portfolio through clinical… more
- ICU Medical (Southington, CT)
- …development meetings and presents agreed upon regulatory positions. May serve as a lead regulatory representative to an assigned product or project team. * * ... not be discriminated against on the basis of disability. **Title:** * Associate II, Regulatory Affairs* **Location:** *CT-Southington* **Requisition ID:**… more
- University of North Carolina- Chapel Hill (Chapel Hill, NC)
- …Salary Range: Dependent on Qualifications/Experience Position Summary/Description: The purpose of Regulatory Associate is to facilitate the conduct of oncology ... clinical trial management system (OnCore) and eRegulatory binder (Florence). The Regulatory Associate also includes involvement in process improvements and… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- **Job Description Summary** The Associate General Counsel, Regulatory Law and Compliance will be a member of the Regulatory Law Group and will report to the ... grow and become your best self. Become a **maker of possible** with us. The Associate General Counsel, Regulatory Law and Compliance will be a member of the… more
- Bristol Myers Squibb (Princeton, NJ)
- …5 years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading ... assessing regulatory risk, and developing global filing strategies. + Co- lead marketing application submission teams for indications that are at regulatory… more
- LSI Solutions (Victor, NY)
- …Specialists I, II, III, and Senior: Base Level from the prerequisite role ( Regulatory Associate ) Essential Functions: + Understand and maintain LSI file ... a backup to the complaint coordinator as needed. + Lead regulatory training sessions for other teams...- Labeling Area: Base Level from the prerequisite role ( Regulatory Associate ) Essential Functions: + Accurately complete… more
- Novo Nordisk (Princeton, NJ)
- …regulatory agencies. Supervise designated personnel. Relationships Report to the Director/ Associate Director/ Lead Regulatory Scientist/Sr. Manager ... related experience; including hands on related pharmaceutical or medical device /pharmaceutical combination product experience and actual regulatory experience… more
- Dr. Reddy's Laboratories (Middleburgh, NY)
- …traditional background. **Job Description** **Job Summary** We are looking for Manager / Lead Associate Quality Control to provide support to the Middleburgh ... options to satisfy unmet medical needs, we are dedicated to helping people lead longer and healthier lives. We are seeking dynamic and energetic individuals ready… more
- Integra LifeSciences (Plainsboro, NJ)
- …challenging what's possible and making headway to help improve outcomes. The Warehouse Lead operator will verify and keep records of all incoming and outgoing ... inventory locations, and perform all associated transactions in ORACLE. The Warehouse Lead will perform all required duties in compliance with company policies, US… more
- Abbott (Alameda, CA)
- …way people monitor their glucose levels with our new sensing technology. The Lead Clinical Research Associate manages the design, execution, and monitoring of ... design, training and monitoring of Abbott sponsored external clinical studies for regulatory and commercial access. + Manage in identification and qualification of… more
- Lilly (Indianapolis, IN)
- …in medical device manufacturing. + Understanding of basic requirements of regulatory agencies such as the FDA, DEKRA, and OSHA. **Additional Preferences:** + ... the world. **Position Brand Description:** Are you ready to lead the charge in shaping the future of manufacturing...the future of manufacturing at Eli Lilly? As an Associate Director of Engineering, you'll be at the forefront… more
- Amgen (New Albany, OH)
- …and our aggressive corporate sustainability goals. The successful Engineering Process Equipment Lead will have extensive experience in Device Design and Assembly ... for a career you can be proud of. Senior Manager of Engineering - Process Equipment Lead **Live** **What you will do** Let's do this. Let's change the world. In this… more
- Lilly (Indianapolis, IN)
- …and guidances for assigned country/region, assess impact with input from Regional Regulatory Scientists, Device Regulatory Scientists, and Labeling Process ... subject matter expert and resource for other GRA colleagues (eg, Regional Regulatory Scientists, Device Regulatory Scientists, Product Communication… more
- Bristol Myers Squibb (Madison, NJ)
- …medical device , and/or translational development processes, with ability to lead supportive project management processes + Strong understanding of global ... the patients and health care providers we serve. The Associate Director, Technical Management, reports to the Technical Management...regulatory requirements for companion diagnostic device development… more
- AbbVie (Branchburg, NJ)
- …Team (IEST) lead , Clinical Program Lead and Clinical Science Lead and Clinical Scientist. The Associate Director, Clinical Development should expect to ... on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director, Clinical Development will have global or regional responsibilities and… more
- Lilly (Concord, NC)
- …of the Parenteral/ Device Assembly and Packaging areas as well as lead / assist in operations readiness programs (eg Material procurement and definition, training ... solutions to improve or meet key performance indicators (KPI) for the area. + Lead area tours to support business reviews, regulatory audits, or network… more
- Lilly (Durham, NC)
- …reports, procedures, deviations, technical reports, change controls, etc. + Partner with Associate Director for Device Assembly to set cohesive QA organization ... to make life better for people around the world. Associate Director - Quality Assurance (QA) Packaging is responsible...up, and validation of the packaging processes in the Device Assembly and Packaging (DAP) production area at Lilly… more
- Lilly (Indianapolis, IN)
- …to: Clinical Laboratory and Diagnostics, such as imaging, ECGs and connected device requirements. + Manages global regulatory inspection activities, including ... cross-functional collaboration with a variety of business partners. Furthermore, the Associate Director will spearhead a team dedicated to supporting the portfolio,… more
- L'Oreal USA (Clark, NJ)
- …/ Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 187395 Associate Principal Scientist, Cosmetics Product Safety & ... Clark, NJ Research & Innovation Full - Time 22-Aug-2024 Position Title: Associate Principal Scientist, Cosmetics Product Safety & Toxicology, L'Oreal Research &… more
- BioFire Diagnostics, LLC. (Salt Lake City, UT)
- …that values collaboration, continuous improvement, and a healthy work life balance. This Associate Software Project Manager will lead a team of software ... part of our team and our mission as a Associate Software Project Manager! bioMerieux - Salt Lake City...execute test plans. They are expected to understand the regulatory requirements regarding medical device software development… more