The Position We advance science so that we all have more time with the people we love. This role is based in the Regenerative Medicine research department which is dedicated to developing world class products for people with autoimmune and degenerative diseases. We do groundbreaking research in the field of regenerative processes, using cutting edge techniques to understa

Collection and organization of technical data from equipment manufacturers, equipment users, and engineering personnel. Timely completing tasks and work orders with appropriate documentation according to Standard Operating Procedures, applicable standards, guidelines, practices, and policies. Safe operation of tools and shop equipment and safe execution of work in the fie

We are seeking a Microbiologist with experience in Research and Development. You will be a key contributor and critical to the success of the company. As part of the Microbiology team, you will be responsible for designing, documenting, and testing both instruments and consumables to support the company's product lines. You will be responsible for executing protocols and

Preparation and analysis of routine and non routine HPLC, LC MS and LC UV samples. Method development for HPLC/LC MS/LC UV analyses. Responsible for accurate evaluation, interpretation, and verification of LC UV and LC MS analyses. Preparation of analysis reports. Perform general maintenance on the LC MS and LC UV instruments to ensure the LC instruments remain operationa

The Position We advance science so that we all have more time with the people we love. The Clinical Pharmacology (CP) Scientist 3 is responsible for the delivery of PK/PD analyses and reports for their assigned development project[s] in order to ensure that appropriate dose/route/schedule decisions are made for patients. S/he typically works under the supervision of a CP

The Position The Opportunity This Job is an Individual Contributor position. In the position of Regulatory Program Director in Roche / Genentech Pharma Technical Regulatory (PTR), you will be accountable for Health Authority interactions pertaining to CMC Information (i.e. CMC information in an IND, IMPD and NDA/BLA/MAA filings), as well as informational and pre submissio

This Manager Level role will support the execution of the WWRD GxP Audit Program with heightened focus in pharmacovigilance audit related responsibilities. Primary Responsibilities Participate in audit planning including internal or external audit risk assessment, audit scheduling, development of audit scope/agenda, and managing pre audit meetings Host and manage internal

What You Can Expect As our Manager of Market Analytics, you will play a pivotal role in advancing ENGIE's Distributed Solar and Storage (DSS) projects. Your main focus will be on developing and maintaining revenue forecasts for DSS projects, supporting market strategy, and enabling new market entry. You will collaborate closely with ENGIE's project finance team to ensure

The Associate Scientist I, Neuroscience is responsible for conducting scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of scree

The pay range for this position at commencement of employment is expected to be between $144,000 $216,000/year; however, while salary ranges are effective from 1/1/23 through 12/31/23, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to

The Senior Director of Clinical Development provides leadership and individual contributions in conceptualization, design and execution of clinical studies to 1) effectively support development and improvement of new Karius product features and new products; and 2) advance clinical evidence that accelerates adoption and reimbursement for Karius products. This work will be

Comprehends, manages, and executes the commercial Promotional Review Committee (PRC)/Medical, Legal, and Regulatory (MLR) review process, ensuring all tactical plans are implemented in compliance with the promotional guidelines and hold all stakeholders accountable by reinforcing the process Work with Marketing/Commercial to coordinate and prioritize materials for Promoti

You will be responsible for preparingmaterials in the laboratory to discover new catalysts and processes that deliver value to the Company's businesses. Specifically, synthesize catalysts using conventional and high throughput techniques and equipment and a variety of preparative methods. Develop new HT workflows for catalyst preparation. You will plan experiments in coll

Cryo Nerve Block Territory Manager San Francisco/San Jose Northern California, CA, USA San Francisco Bay Area, CA, USA San Francisco, CA, USA San Jose, CA, USA Virtual Req #1962 Thursday, February 29, 2024 Who We Are AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electro

The Lead, Regulatory Operations is responsible for managing Regulatory Affairs activities (nonclinical, clinical and CMC) for assigned investigational development products from preclinical candidate designation through product approval, including regulatory submissions. This individual is responsible for maintaining an in depth awareness of relevant federal and internatio