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15 jobs found for Biotech Job Sites

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  • at site To baseline plans like design concept for facilities, equipment - regulatory compliant, Technical approval. To manage new project, facilities with an advance technology and automation with capacity demand and resources like utilities with all compliance to safety aspects. To make project schedule, Overall 15-20 years experience in Domain like Pharmaceuticals, Biotech and Medical Devices Companies ...

  • at site To baseline plans like design concept for facilities, equipment - regulatory compliant, Technical approval. To manage new project, facilities with an advance technology and automation with capacity demand and resources like utilities with all compliance to safety aspects. To make project schedule, Overall 15-20 years experience in Domain like Pharmaceuticals, Biotech and Medical Devices Companies ...

  • at site To baseline plans like design concept for facilities, equipment - regulatory compliant, Technical approval. To manage new project, facilities with an advance technology and automation with capacity demand and resources like utilities with all compliance to safety aspects. To make project schedule, Overall 15-20 years experience in Domain like Pharmaceuticals, Biotech and Medical Devices Companies ...

  • at site To baseline plans like design concept for facilities, equipment - regulatory compliant, Technical approval. To manage new project, facilities with an advance technology and automation with capacity demand and resources like utilities with all compliance to safety aspects. To make project schedule, Overall 15-20 years experience in Domain like Pharmaceuticals, Biotech and Medical Devices Companies ...

  • commissioning. To implement HSE practices as per group / site requirements B.E/B.Tech-Mechanical Engineering with 6 - 10 years of experience in green / brown field projects. Experience in green field & brown field projects is mandatory. Technical Competencies: Essentials: Practical experience in executing biotech projects. He should have knowledge in HVAC & Piping design. He should have optimum knowledge in ...

  • are complied with the approved project specification/standards. To assess & report risks associated related to MEP Installations or general project to project manager. To monitor & report to manager on site progress and quality of MEP (mechanical, electrical, plumbing) work in line with contractors schedule Overall 10 -15 years experience (Domain Pharmaceuticals, Biotech, Medical Devices, Design Engineering ...

  • are complied with the approved project specification/standards. To assess & report risks associated related to MEP Installations or general project to project manager. To monitor & report to manager on site progress and quality of MEP (mechanical, electrical, plumbing) work in line with contractors schedule Overall 10 -15 years experience (Domain Pharmaceuticals, Biotech, Medical Devices, Design Engineering ...

  • are complied with the approved project specification/standards. To assess & report risks associated related to MEP Installations or general project to project manager. To monitor & report to manager on site progress and quality of MEP (mechanical, electrical, plumbing) work in line with contractors schedule Overall 10 -15 years experience (Domain Pharmaceuticals, Biotech, Medical Devices, Design Engineering ...

  • are complied with the approved project specification/standards. To assess & report risks associated related to MEP Installations or general project to project manager. To monitor & report to manager on site progress and quality of MEP (mechanical, electrical, plumbing) work in line with contractors schedule Overall 10 -15 years experience (Domain Pharmaceuticals, Biotech, Medical Devices, Design Engineering ...

  • documented and versatile Develop and implement long range plans for process control improvements. Guide and train area personnel on process control methodology in order to assist process control improvement efforts. Support process control related activities of site capital projects. Provide process

  • documented and versatile Develop and implement long range plans for process control improvements. Guide and train area personnel on process control methodology in order to assist process control improvement efforts. Support process control related activities of site capital projects. Provide process

  • documented and versatile Develop and implement long range plans for process control improvements. Guide and train area personnel on process control methodology in order to assist process control improvement efforts. Support process control related activities of site capital projects. Provide process

  • documented and versatile Develop and implement long range plans for process control improvements. Guide and train area personnel on process control methodology in order to assist process control improvement efforts. Support process control related activities of site capital projects. Provide process

  • documented and versatile Develop and implement long range plans for process control improvements. Guide and train area personnel on process control methodology in order to assist process control improvement efforts. Support process control related activities of site capital projects. Provide process

  • Nos. Job Location: Chandivali, Mumbai Designation: Manager Regulatory Affairs Education: B.Pharm/ M.Pharm Experience: 10-15 years experience into Pharma Regulatory Industry: Pharma/ Biotech Function Area: Regulatory Affairs Key Skills: ROW, CTD, ACTD, pharma regulatory affairs, RA, manager, Please refer the given job description for detailed information

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