- Lilly (Pleasant Prairie, WI)
- …solutions that impact the site and align with corporate objectives. The Associate Director, Quality Assurance, will also provide computer system quality assurance ... in operational processes, and Computer System Validation methodologies to ensure regulatory compliance, consistency, and sustainment. The Site Data Leader is… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The Associate Director, Cleaning Validation is responsible for leading and executing Cleaning Validation (CV) activities for a large-scale ... biologics manufacturing facility in compliance with regulatory requirements, including 21 CFR Parts 11, 210, and 211, as well as ASTM E2500 guidelines. This role… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …inspire you and empower you to shine? Join us as an Associate Medical Director, Clinical Science, Neuroscience- Pulmonologist/Neurologist in our Cambridge, MA ... a vital contributor to our inspiring, bold mission. **POSITION OBJECTIVES:** The Associate Medical Director leads and drives strategy for the overall global… more
- Pfizer (New York, NY)
- …in Clinical Pharmacology! Our Clinical Pharmacology Team is looking for an Associate Director to support the exciting portfolio in Internal Medicine. Our team ... members champion the innovative use of MIDD for efficient drug development and robust decision-making. A great environment for learning and professional growth!… more
- Parexel (Concord, NH)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local ... in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and… more
- Merck (West Point, PA)
- …degree is preferred. + Leadership experience with working knowledge of device, biologic/ drug product, and process development including regulatory submission and ... **Job Description** ** Associate Principal Scientist - Device Technical and Engineering...Process Development (DPPD) Team designs, develops, and commercializes novel biologic/ drug /vaccine - device enabled combination products to achieve safe… more
- Vigor, LLC (Portland, OR)
- …work history and/or applicable education will be considered in lieu of work experience. Associate 2 Proficient in both Fire Watch and Associate 1 job duties. ... of a Journey Level employee or Supervisor. May perform Associate 1 or Fire Watch duties. Must acquire three...to detail: Must perform all tasks in compliance with regulatory agency standards. + Flexibility: May move from one… more
- Banner Health (AZ)
- …oversight of reports that are sent to government regulators. In addition, the associate advisor is responsible for disseminating regulatory policy updates to ... by offering remote and hybrid work settings. The Government Programs Project Associate Advisor will be responsible for assisting with the management, tracking, and… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …and services in more than 110 countries and regions. The Clinical Research Associate assists in the management of the clinical monitoring process to ensure site ... adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols....to ensure data integrity. + Reconciles clinical supplies and drug accountability records at study sites. + Identifies and… more
- Merck (Wilson, NC)
- …We are seeking a highly motivated individual for the role of Associate Director Engineering - MDCP Technical Lead, supporting the Wilson Packaging Technical ... automation, packaging process, equipment and components, equipment qualification and related regulatory requirements are a must for this position. The ability to… more