- Abbott (Plymouth, MN)
- …product Design History File. + Comply with US Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, ... of leadership experience in Engineering, R&D, and/or Quality within a medical device /biomedical, high technology, and/or regulated industry + 5+ years in Program… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …has sufficient understanding of regulations and GCP requirements for drug development, advanced knowledge of Electronic Data Capture/related applications and ... ensure effective cross-functional collaboration and proactive communication throughout the drug development process. + Collaborates within the function and… more
- Takeda Pharmaceuticals (Lexington, MA)
- …profound GRA CMC knowledge underpinned by a deep understanding of global drug development and regulatory essentials to address and overcome challenges that arise ... Advanced Degree (MS), with Ph.D. preferred. + 15+ years of seasoned biopharmaceutical/ device industry experience or with a regulatory agency, while leading major… more
- Takeda Pharmaceuticals (Boston, MA)
- …the Company-wide patient safety expert for assigned pharmaceutical / biological / drug - device combined products, accountable for the safety strategy and major ... + At least 5 years of experience in pharmaceutical industry within Drug Safety/Pharmacovigilance, with both investigational and marketed products. + At least 3… more
- Southern Glazer's Wine and Spirits (Honolulu, HI)
- …of our Top Shelf Benefits, including comprehensive medical and prescription drug coverage, dental and vision plans, tax-saving Flexible Spending Accounts, disability ... typing/keyboarding using a computer (eg, keyboard, mouse, and monitor) or mobile device + Physical demands with activity or condition may include walking, bending,… more
- Lilly (Indianapolis, IN)
- …+ Preference for experience/familiarity with multiple manufacturing technology platforms (API, drug product, device ) + Preference for experience with both ... pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (eg, healthcare and/or dependent day care… more
- Stryker (MD)
- …Review regulatory compliance requirements for changes affecting product submission and device manufacturing in global markets + Implement regulatory system changes ... other relevant factors. Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident… more
- AbbVie (North Chicago, IL)
- …pumps, enteral and sub-cutaneous tubing, pump carrying accessories, and other drug administration system accessories. Products may be produced by AbbVie plants ... Quality Assurance strategy for NPI projects to support development of device and combination products. Implements agreed strategy. + Communicates and negotiates… more
- BeOne Medicines (San Mateo, CA)
- …years of relevant pharmaceutical or biopharmaceutical industry experience in innovative drug CMC development, manufacturing, Quality, etc. including minimum 8 years ... manufacturing, QC, QA, etc.). * Experience in gene/cell therapy or/and medical device is a plus. * In-depth knowledge of ICH requirements, global regulatory… more
- SUNY Geneseo (Geneseo, NY)
- …Services. The Endpoint Systems Analyst works independently under the direction of the director . The director routinely meets 1:1 to provide guidance and ... (https://www.youtube.com/watch?v=0E28zJDeYTU) Background Investigation Statement All applicants are subject to drug and criminal background checks. See our full Background… more