- Lilly (Stamford, CT)
- …make life better for people around the world. **Purpose:** The purpose of the Senior Director , Global Regulatory Affairs, Global Regulatory Lead (GRL) role is to ... regulatory strategy documents by leveraging team expertise, as well as scientific, drug / device clinical development and knowledge from health authorities such as… more
- Lilly (Pleasant Prairie, WI)
- …and quality improvements, increased productivity, and variability reduction. **Responsibilities:** The Senior Director , Quality Assurance, serves as the Site ... this role establishes the site's quality objectives, priorities, and roadmap. The senior director leads and/or participates in the assessment, development, and… more
- Lilly (Indianapolis, IN)
- …plant floor data solutions, and implementation of cyber security programs. The Senior Director position has overall responsibility for the supervision, ... and productivity improvement, and overall customer service. The GPACE Senior Director oversees the area's workload, customer...is expected that this role will support the Parenteral Device Network (PDN) and the sites within this network… more
- Fresenius Medical Center (Lawrence, MA)
- **PURPOSE** **AND** **SCOPE:** The Senior Director , Sales Training & Development is responsible for leading the strategy, design, and execution of sales training ... development, along with experience navigating complex healthcare markets. The Senior Director will apply an enterprise mindset,...including at least 5 years in pharmaceutical or medical device sales training and education, and 5+ years in… more
- Sandia National Laboratories (Tonopah, NV)
- …law. NNSA Requirements for MedPEDs: If you have a Medical Portable Electronic Device (MedPED), such as a pacemaker, defibrillator, drug -releasing pump, hearing ... national lab offices is required and expected. The Test Director is responsible for following established range processes and...Sandia is required by DOE to conduct a pre-employment drug test and background review that includes checks of… more
- Caris Life Sciences (Austin, TX)
- …bigger than yourself, Caris is where your impact begins.** **Position Summary** The Senior Director , Market Access Medical Policy is the expert in Caris ... + A minimum of 8 years of relevant experience from biotech, medical device , or a molecular diagnostic laboratory. + Deep scientific understanding and practical… more
- Takeda Pharmaceuticals (Boston, MA)
- …Company-wide patient safety expert for assigned oncology pharmaceutical / biological / drug - device combined products, accountable for the safety strategy and ... to the Takeda Safety Board and similar forums. The Senior Medical Director will be a key...support of safety update regulatory submissions, investigational and new drug applications and interactions with regulatory authorities worldwide. +… more
- Takeda Pharmaceuticals (Boston, MA)
- …work with portfolio teams to optimize top-tier development cycle times to accelerate drug to patients. **Accountabilities:** + Senior level R&D CMC portfolio ... for facilitating the Pharm Sci CMC Governance advisory board, comprised of senior -level CMC experts to advise Pharm Sci teams towards winning CMC development… more
- GE HealthCare (Waukesha, WI)
- …quality objectives, metrics, reporting and operating mechanisms. + People leader with senior level direct reports. Deep expertise within quality to drive compliance ... experience is preferred. Demonstrated understanding or aptitude to understand Medical Device QMS requirements and regulatory requirements including but not limited… more
- Kestra Medical Technologies, Inc (Kirkland, WA)
- …has over 400 years of experience in the external and internal cardiac medical device markets. The company was founded in 2014 by industry leaders inspired by the ... opportunity to unite modern wearable technologies with proven device therapies. Kestra's solutions combine high quality and technical performance with a wearable… more