- Eisai, Inc (Exton, PA)
- …difference. If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading and ... as supporting technology transfer to external partners (as required). The Associate Director sets strategic directions and project priorities, providing scientific… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJOB DESCRIPTION SUMMARYThe Associate Principal Scientist is a DVM/VMD and/or PhD whose primary function is to design, coordinate, monitor, and report ... Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies.The Associate Principal Scientist is the primary clinical study team leader and… more
- Genmab (NJ)
- …a fit? Then we would love to have you join us!The RoleAs Senior Clinical Trial Associate (Sr CTA) you play a key role in supporting Clinical Trial Team (CTT) and ... smooth trial operations. The Sr CTA assists with study documentation , regulatory compliance, communication between stakeholders, and overall trial coordination.… more
- Merck & Co. (Millsboro, DE)
- Job DescriptionOur company seeks to add an Associate Director. Veterinarian Services at our Millsboro, Delaware location. This position will have overall ... maintenance of animal facilities. This position is responsible for providing data, documentation , and other information as needed for annual reports to Federal… more
- Merck & Co. (Rahway, NJ)
- …of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Rahway, New Jersey research facility.- ... The Associate Principal Scientist is a laboratory-based scientific role tasked...for successful transfer of assays. Plan assay optimization and documentation to meet program deadlines.Authoring and reviewing internal technical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director, Laboratory Data Management is accountable for the end-to-end delivery ... approvals.- Accountable for maintenance and adherence to laboratory data management documentation and guidance such as DS LNR Worksheet template, Textbook Range… more
- Merck & Co. (Rahway, NJ)
- …audit and assurance services.Position Overview / Function and ResponsibilityThe Associate Director:Leads a small team through financial and compliance audits ... business scenarios following a risk based approach and maintains supporting documentation .Coaches in the skill of detecting, analyzing, quantifying and reporting… more
- Twist BioScience (South San Francisco, CA)
- …join our Twist Bioscience Operations Team in South San Francisco. The Manufacturing Associate , NGS TE will perform basic molecular biology workflows in a highly ... keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …to support manufacturing operations. Focus areas may include Training, Documentation , Deviations, Change Control and Projects. Drives the coordination and ... process/equipment improvements and data trending/analysis Review/approval of completed process documentation Ability to train others on the manufacturing process and… more
- Merck & Co. (Durham, NC)
- Job Description Position Description: The Associate Director, HVAC & Utilities Engineer is a member of the Plant Engineering team providing technical support to the ... of design & engineering records and related Good Manufacturing Practices documentation , identifying and resolving discrepancies in a timely manner, and implementing… more
- Aequor (Thousand Oaks, CA)
- …Proficiency in SAP and MES for batch record review and sampling documentation Strong attention to detail and excellent communication skills Values continuous ... in the pharmaceutical industry Must have experience with GMP processes and documentation . Without that fundamental skillset the training for document review tasks,… more
- Merck & Co. (Rahway, NJ)
- …independently conducting and directing the planning, execution, analysis, and documentation of all stages of cell culture process commercialization.Experience with ... model qualification (SDMQ) and process characterization (PC).Experience authoring technical documentation in support of the following: process characterization (PC),… more
- Merck & Co. (Rahway, NJ)
- …to GMP procedures, strong attention to detail in completing GMP documentation , proficiency in electronic systems, and participation in continuous improvement ... transports required processing equipment, materials, supplies, and products.Executes all documentation and clerical functions necessary to maintain good manufacturing… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …process/equipment improvements, sample testing and data trending/analysis Review of completed QC documentation Ability to assist with training to support on the QC ... equipment/processes Revise documentation (SOP, forms, reports, notebooks) associated with the testing of in-process/product samples, requiring some direction… more
- Merck & Co. (North Wales, PA)
- …including analysis/modeling datasets, tables, listings, figures and associated documentation .Ensure programmatic traceability from data source to analysis/modeling ... result.Maintain and manage a project plan including resource forecasting.Support the development of programming standards to enable efficient and high-quality production of programming deliverables.Represent statistical programming on process improvement… more
- Merck & Co. (Durham, NC)
- …- 6:30 AM) rotation (2-2-3). -The Vaccine Manufacturing Facility Production Associate is an excellent opportunity for experienced individuals that are interested ... through hands on processing activities. Key responsibilities for the Production Associate include the execution of aseptic processing requirements, adherence to Good… more
- AUROBINDO (Dayton, OH)
- …at economical prices to make this a healthier world to live in.Job OverviewIPQA Associate Level I will support and assist the day to day activities related to ... and labeling material, water sampling, CV sampling, completion of appropriate documentation , registering in LIMS, deduction of sampling quantity in ERP, promptly… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …scope Documents and archives work in accordance with Good Documentation Practice Identifies continuous improvement opportunities Present standard requests during ... with others Other duties as assigned Qualifications Education and Certifications Associate 's degree in a scientific discipline required Bachelor's degree in… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …marketed products Track applications through FDA reviewing divisions Work with project associate on compilation of information and supportive documentation for ... FDA meetings Liaison between NNI and NNAS departments for preparation of documentation necessary for submission of applications Maintain meeting documentation … more
- Novo Nordisk Inc. (West Lebanon, IN)
- …laboratory investigations Documents and archives work in accordance with Good Documentation Practice May support report writing activities Performs all job duties ... as assigned Qualifications Education and Certifications: High School Diploma required Associate 's degree in a scientific field preferred Work Experience: High School… more
Related Job Searches:
Associate,
Associate Documentation Specialist,
Associate Technical Documentation Specialist,
Clinical Documentation Associate,
Documentation,
Loan Documentation Associate,
Sr Associate Clinical Documentation,
Temporary Clinical Documentation Associate