Travel as necessary to meet project needs.Some positions have little or no travel).Ability to follow a written method of procedure (MOP).Ability to pe..Share
Additional Career Opportunities: Upon successful completion of first term contract, you are guaranteed up to 5 interviews with your choice 1,200 indus..Share
Perform testing and release of raw materials, excipients, intermediates, and finished products used in drug production; responsible for maintenance an..Share
Title: Polymer Process design Engineer.I am seeking a very experienced Engineer – to drive Process Design in my organization.I am compiling a variety ..Share
At LabCorp we have a passion in helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patient..Share
GLP(良好实验室规范)要求开展实验方案制定、数据记录与分析,确保研发过程的可追溯性和合规性。.DoE(实验设计)等统计工具,具备工艺建模及数据分析能力(JMP/Minitab等)。.Responsible for upstream/downstream biopharmaceutical proc..Share
Category Laboratory Location Brick, New Jersey Job function Operations Job family Laboratory Operations Shift Night Employee type Regular Full-Time Wo..Share
We are looking for an experienced and strategic Senior Buyer to oversee the procurement of essential raw materials, indirect materials, MRO, services,..Share
Overview 3rd shift opportunity requires training on 1st and 2nd shift before you\'re moved permanently to 3rd shift. Responsibilities Ensures opera..Share
PLESE NOTE:Need to be a U.S. Citizen with the ability to communicate clearly in English. Only local NJ/NYC area people will be considered. Must reside..Share
Manufacturing Engineer - PLC and Controls We are seeking a diligent and skilled Manufacturing Engineer to join our established company based in Whippa..Share
Lead structure-based drug design: Perform molecular docking, virtual screening, and binding mode analysis using Schrödinger/MOE.Develop ADMET predicti..Share
Technical Operations Manager - Clinical Cell and Vaccine Production Facility.The Clinical Cell and Vaccine Production Facility (CVPF) and Center for A..Share
GMP????,????????????????????????????.FDA/EMA/WHO/ICH/NMPA?????,??????????????????? 6.Participate in the full process of technology transfer from R&D t..Share