- Cipla (Fall River, MA)
- …following: Assist in the development, implementation, and maintenance of the QMS in line with GMP (Good Manufacturing Practice) and regulatory requirements (eg, ... and review of the Annual Product Quality Review . Fulfil the requirement of regulatory submission...applications such as Microsoft Office tools, SAP, and other business applications. Must be able to influence decision-making and… more
- Heritage Bank (Portland, OR)
- …officers and business unit management, and/or other functional areas under review to present risk issue findings and secure commitments for resolution of areas ... Review Officer - 3+ years recent experience in commercial lending, credit/loan review and/or similar position requiring strong business knowledge and credit… more
- Novo Nordisk Inc. (Minneapolis, MN)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From healthcare provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Merck & Co. (Rahway, NJ)
- …scale potent material handling, and the ability to integrate new technologies and cell- line platforms. This role will be a member of the Process Automation team, ... to design, install, and qualify new equipment to support GMP clinical production. Write, review or execute test documents. Limited off shift work may be required to… more
- Merck & Co. (South San Francisco, CA)
- …point in the drug development process, working closely with scientific, regulatory , statistical, and modelling colleagues across the organization to translate the ... developmentDevelopment of biomarker strategies through cross-functional teams that provide line -of-sight from First-in-Human studies through clinical Proof-of-Concept.- This includes… more
- Aequor (Golden Valley, MN)
- …and executing a variety of projects, including new product launches, line extensions, and packaging improvements. You will collaborate with cross-functional teams ... to launch new products and packaging solutions that drive business results. The Central Pack team, part of Integrated...on a variety of project types, including Brand Strengthening ( line extensions, in & outs, package size variety, cost… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …standards and timelines and that quality of data is suitable for regulatory submission. The SDL collaborates with cross-functional stakeholders and the Metrics, ... on clinical trial execution. Outside interfaces may include other Daiichi-Sankyo business groups and subsidiaries in the US and abroad, governmental, academic,… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …focused mindset, in order to prepare for potential internal or external audits in line with GMP and FDA requirements. Incumbent will be expected to excel in a ... can change quickly, while also taking into consideration the downstream effects and regulatory requirements of actions. This is an onsite role Monday-Friday based at… more
- Takeda Pharmaceutical (Social Circle, GA)
- …commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all ... Final documents are archived and may be included in or support regulatory submissions, and made available during internal and external regulatory /compliance… more
- University of California Santa Cruz (Santa Cruz, CA)
- …and access on- line application: ... application process or if you are experiencing difficulties when applying, please review the Applicant Resources on our website. How to Apply Troubleshooting Tips… more
