- Merck & Co. (Rahway, NJ)
- Job DescriptionJob Description The Senior Scientist , Device Design Control Lead, is a crucial member of our team, responsible for spearheading design control ... concept through launch and post-market surveillance. Key Responsibilities and Activities: The Senior Scientist , Device System - Device Design Control will be… more
- Merck & Co. (Rahway, NJ)
- …The engineer will be expected to exhibit a mindset of safety and quality compliance, which will include following current Good Manufacturing Practices (cGMPs), and ... participating in risk assessments, deviation investigations, and Good Documentation Practices (GDocP).-A high level of innovation, creativity, and self-initiative along with the ability to plan and organize activities are expected.- Successful candidates will… more
- Merck & Co. (North Wales, PA)
- …that project plans are executed efficiently with timely and high quality deliverables.-For assigned projects the position serves as the statistical programming ... Skills and Experience: Demonstrated success in the assurance of deliverable quality and process compliance. Strong working knowledge of reporting processes (SOPs)… more
- Merck & Co. (North Wales, PA)
- …benefit of patients and global human health. This position provides high quality statistical programming analysis and reporting deliverables for global PK modeling ... and simulation stakeholders spanning all therapeutic areas. The senior programmer will gather and interpret user requirements, retrieve the required data, transform… more
- Merck & Co. (Rahway, NJ)
- …we develop are as diverse as the team developing them, and in this Senior Scientist role, the chosen candidate will leverage fundamental process modeling, ... the fabric of our company process development culture. This Senior Scientist role is a scientific position...drive enhanced decision making for improving the speed and quality of development for diverse medicines and vaccines.In this… more
- Merck & Co. (Rahway, NJ)
- …integrating state-of-the-art technology and applying rigorous scientific and ethical standards.The Senior Director ( Senior Principal Scientist ) has primary ... (pre-clinical to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including… more
- AUROBINDO (Dayton, OH)
- …and process scale-up Qualifications - Skills & Requirements3-5 years of Senior Scientist Formulation development and process developmentExperience in the ... based on Total Prescriptions Dispensed. (We are#27 in 2010)Job OverviewThis is a Senior Formulation Scientist role in Generic Pharma, product development with 3… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOphthalmology Clinical Scientist :Job SummaryThis position leads the scientific planning and execution of one or more clinical trials or significant ... execution of clinical protocol(s). This may include:Serving as the lead clinical scientist on the clinical trial team.Leading medical monitoring team in review and… more
- Tris Pharma (Monmouth Junction, NJ)
- …New Jersey, Tris has an immediate opening for a Method Validation R&D Senior Scientist ISummary:The Method Validation (MV) Research and Development (R&D) ... Senior Scientist I, under minimal guidance, performs...and advances required documentations, in liaison with Product Development (PD)/ Quality Assurance (QA)/ Quality Control (QC)/Regulatory Affairs, including… more
- Merck & Co. (San Diego, CA)
- …preparation, submission, and follow-up of regulatory applications and ensure quality and compliance across all documentation.Interact independently with regulatory ... agencies (FDA, EMA, etc.), including leading meetings, teleconferences, and written communications.Lead cross-functional teams in preparation for regulatory advisory committee meetings and may include a speaking role.Coordinate regional regulatory strategy and… more
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