Designing, Detail Engineering, Planning, Execution, Commissioning and Validation Activity of API Process plant equipment, Utility equipment, HVAC systems, Water systems etc Daily co-ordination with Project purchase, various contracting agencies. Industry Pharma/Biotech/Clinical Research
generation of Project funnel Visiting project sites, collection of data Showing Samples to builders Sales generation & closures 3. Developing Architects & Interior Designers, meeting them on regular basis Briefing them with Products and new developments, generating leads for ROs , Softeners, Swimming pools
2. Do and oversee lab trials and field trials with concessionaires and contractors and make trial reports 3. Execute soil stabilization, Bond coats and Asphalt additives field stretches 4. Observe typical practices / challenges at the contractors site and suggest ideas to offer innovative
in both AM & Development projects. 4) Below to be excluded while Job Postings on Portals/SNS sites. 5) Experience and understanding of web services and XML technologies (WSDL, SOAP, REST, XML, XSD, XSLT, WSIL, WSRP, WS-Security) 6) Experience with Web Services and interacting with databases (Oracle, SQL
of the biotech/biopharma production chain, creating a complete end-to-end workflow with enhanced customer service, a simplified interface and a leading e-commerce and distribution platform.MilliporeSigma operates 65 manufacturing sites worldwide and employs more than 19,000 people in 66 countries. This geographic reach ...
50% of the time to sub suppliers and customer sites for project execution Knowledge on Quality management systems Benefits?Allowances Client Introduction?About the CompanyPall Corporation is a global leader in high-tech filtration, separation, and purification, serving the diverse needs of customers
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