- Sumitomo Pharma (Morrisville, NC)
- …, transfer execution, and final approval. + Create and maintain cell biologics -medical device combination product design history files from early-stage ... **Sr. Director , Cell Quality** Sumitomo Pharma America (SMPA) is...technology platforms and advanced analytics capabilities to accelerate discovery, development , and help bring novel therapies to patients sooner.… more
- Sanofi Group (Cambridge, MA)
- …development , monitoring and updating of standards and processes related to drug, device , and biologics US AdPromo regulations and guidances. Other Position ... About the Role The Associate Director , US Regulatory Affairs (RA) serves as the...for the advertising and promotion of prescription drugs and biologics . Essential Functions + Represents Global Regulatory Affairs (US… more
- AbbVie (Worcester, MA)
- …may have the complexity of multiple types of productions (API, Fin Goods, Biologics , Packaging, Device , etc.). + Represents the decision-making authority on job ... 15+ years of combined experience in Manufacturing, QA, QC, R&D in pharmaceutical, biologics , device or chemical industry. + 10+ years of supervisory/technical… more
- Lilly (Cambridge, MA)
- …Life Science or related field with 10+ years of drug delivery and device design and development . + Experience on leading technical teams. **Additional ... matter authorities. Together this group will own new investments in delivery and device technologies that span all therapeutic areas. As drug therapies become more… more
- AbbVie (Barceloneta, PR)
- …may have the complexity of multiple types of productions (API, Fin Goods, Biologics , Packaging, Device , etc.). + Represents the decision-making authority on job ... + 15+ years of combined experience in Manufacturing, QA, QC, R&D in pharmaceutical, biologics , device or chemical industry + Must have a basic understanding and… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. **Associate Director ** **; CMC, Device Development Program Manager** **Functional Area: ... cross-functional team members to execute. + Solid understanding of drug development , device development , biologics manufacturing, and global operations.… more
- Organon & Co. (Jersey City, NJ)
- …demonstrated application in one or more of the following areas; Medical Device /Combination product, Biologics , Vaccines, API's, Non-sterile Drug Product or ... **Job Description** **The Position** The Associate Director is responsible for achieving and maintaining qualification/certification status through robust training… more
- Bristol Myers Squibb (Devens, MA)
- …and/or business analytics certificate(s) + A high-level understanding of integrated drug development of biologics and/or pharma compounds. + Technical acumen in ... personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director (AD) Quality Product Lead (eg, QPL, Quality Product Steward)… more
- J&J Family of Companies (Malvern, PA)
- …Director , Cell Therapy Lab Automation - 2406182172W **Description** Janssen Research & Development , LLC. is recruiting for an Associate Director , Cell Therapy ... product support, and life cycle management of Biotherapeutics. Within TDS, the Analytical Development (AD) Biologics group supports method development and… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , Temperature Strategy & Execution - 2406177829W **Description** Johnson & Johnson Innovative Medicine Research & Development (JJIM R&D), part ... the Johnson & Johnson Family of Companies, is recruiting for an Associate Director , Temperature Strategy & Execution within Clinical Supply Chain (CSC). The position… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …sites. Experience: + Pharmaceutical Quality Manufacturing experience. Solids, Medical Device , Sterile, Biologics , and/or Biosimilars Quality Compliance ... Director , Quality System Compliance Date: Apr 10, 2024...regulations updates, improvement to standards, etc. + Quality Plan development /tracking as required. + Tracking regulatory commitments, creating Investigator… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …Knowledge and Experience + Pharmaceutical Quality Manufacturing: Solids, Medical Device , Sterile, Biologics , and/or Biosimilars Quality Compliance experience ... Sr Director , Global IT Quality Compliance Date: Mar 28,...required. + Demonstrates continuous professional development . + Advanced leadership skills, business strategy, accounatbility, proven… more
- BeiGene (San Mateo, CA)
- **General** **Description:** The Senior Director of CMO and Distribution Logistics, Clinical Supply Chain is responsible for overseeing the Clinical Supply Chain ... and maintain relationship with global Courier/broker vendors. + Oversee the development of the Import permit application strategy globally. + Ensure site/CMO/vendor… more
- Sanofi Group (Bridgewater, NJ)
- The Associate Director RA serves as the regulatory lead on Review Committees (RCs). As the RC RA representative, work with brands on competitively positioning ... Industry Guidelines for the advertising and promotion of prescription drugs, biologics , and devices. **ESSENTIAL FUNCTIONS** + Provide regulatory leadership and… more
- Novo Nordisk (Plainsboro, NJ)
- …to providing medical education and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps us all marching to the ... The Position Manage and oversee all assigned projects/products/processes. Assist the Director /Associate Director in assuring Novo Nordisk compliance with… more
- Philips (Colorado Springs, CO)
- …and providing regulatory guidance for Sustaining and New Product Development /Design initiatives for our Image Guided Therapy Devices/Coronary Vascular team. ... regulatory files and tracking databases as required. + Reporting to the Director of Regulatory Affairs- Coronary Vascular you will collaborate with worldwide… more