- Exela Pharma Sciences, LLC (Lenoir, NC)
- …completionResponsible for drafting and providing technical guidance for the validation program , Policies and SOPs and other master documentsSupport Engineering ... Position Summary:Oversee and lead the validation program for production equipment and processes used to...Masters , or Ph.D. in Biochemistry, Biology, or related science fieldDemonstrated knowledge and application of FDA cGMP/GCP regulations,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and ... for the Clinical Label Development process which includes creation of master label text, translations, and label proofs.Manages the packaging Batch Record… more
- Genmab (Plainsboro, NJ)
- …standards.Therapeutic area experience preferredRequirements - what you must haveBachelor of science degree with relevant specialization; Master of science ... to our business, which is innovative and rooted in science , we believe that being proudly unique, determined to...essential to fulfilling our purpose.Overview The Global Clinical Trial Manager , Team Manager (GCTM-TM) is responsible for… more
- Genmab (Plainsboro, NJ)
- …caring, candid, and impact-driven to our business, which is innovative and rooted in science , we believe that being proudly unique, determined to be our best, and ... is essential to fulfilling our purpose.Genmab is seeking a Clinical Drug Supply Manager to join our Global Clinical Drug Supply (GCDS) Operations Team in Princeton… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and ... Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine interaction with key internal and...and quality metrics and share with study team, Operations Program Lead, and Sr. Director for the compound, on… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and ... audits, regulatory authority inspections, and internal process deviations delivered to program teams by assessing the learnings and proposing solutions to address… more
- Genmab (Plainsboro, NJ)
- …or Master 's degree in privacy engineering, computer engineering, computer science , information systems, or related field of study Computer Science , ... to our business, which is innovative and rooted in science , we believe that being proudly unique, determined to...Risk reporting into the Head of Global Data Privacy Program , will serve a pivotal role at Genmab by… more
- Merck & Co. (Durham, NC)
- …guided by policies, procedures and business plan; receives occasional guidance from manager .Walks down equipment with mechanic or engineer to draft a maintenance ... path forward for least disruption to plant operationsContributes to master shutdown schedule including all maintenance and calibration activitiesSupport departmental… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …deviations & corective actions. Prior experience in Pharmaceutical or Life Science manufacturing facilities is preferred, or experience in related GMP manufacturing ... Relocation assistance is eligible for selected candidate. Relationships Reports to: Manager of Manufacturing Engineering & Validation Number of subordinates with… more
- Beckman Coulter Diagnostics (Miami, FL)
- …80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, ... the Global Product Compliance Engineering Department and report to the Senior Manager in Brea, California responsible for leading the Product Compliance program… more
