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53 jobs found for Hyderabad

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  • Lead entire Plant EHS Only Dip/ BE + Dip in Safety from RLI, NIT etc having 5+yrs exp in entire gamut of Safety, Health & Environment in a large Process / Manufacturing unit & willing to relocate near MEDAK/ Hyderabad, Telungana apply Only Dip/ BE + Dip in Safety from RLI, NIT etc having 5+yrs exp in entire gamut of Safety, Health & Environment in a large Process / Manufacturing unit & willing to relocate near MEDAK ...

  • we have opening in QMS in Solid Oral @ Aurangabad , Indore , Nasik ,Hyderabad. Should have exposure in Audit & Compliance. Compliant and Deviation Management should have face USFDA/MHRA. Qualification:- B.PHARMA/M.PHARMA/M.Sc

  • Job Description 1)Responsible for all Mechanical maintenance of plant (Process Systems) including breakdown modification and Preventive maintenance. 2)Support execution of calibration, Validation, Qualification, Temperature mapping activity. 3)Support Procurement of spares, maintaining inventory of Critical Spares. 4)Coordination with Vendors for Spares / Services. 5)Breakdowns trending & root-cause analysis ...

  • Job Description Responsible for Investigation of deviation, incidence, and change controls, OOS results, on conformity and market complaints. Should be able to handle of Incidents and CAPA Management . To lead validation team members of IQ, OQ, PQ, of process. Cleaning and blending validations Review and approve validation protocols and reports. Change Management. Review of stability data. To Carry out internal ...

  • Job Description 1)Responsible for all Instrumentation systems of plant including breakdown modification and preventive maintenance. 2)Planning and execution of Instrument calibration, Validation, Qualification, Temperature mapping activity. 3)Procurement of spares, maintaining inventory of Critical Spares. 4)Coordination with Vendors for Spares / Services. 5)Troubleshooting & calibration of GE Fanuc, Siemens ...

  • 1.Formulation and aseptic filling and packing operations(execution as per production plan) of Sterile filled biological products. 2.Day To day operations of the packing(execution as per production plan) and dispatch of various products. 3.Well conversant with for pharmaceutical drug manufacturing guidelines like WHO guidelines FDA /MHRA / Eu. 4.Maintenance of GMP records for R&D development and ...

  • Those who know Pro- E, U g and product design and Mould designs they have to be B.Tech Mech + PGTD/PDTD courses from tooling institutes such as IGTR, NTTF, CITD etc., Design Engineers with 3 to 6 years experience Pro- E, U g and product design and Mould designs

  • Expertise in all Production Planning & Departmental Co ordination Related activities + Strength in Wovens + Shirting’s & Telugu Speaking is a must Key Skill:-Factory Manager, PPC, Production, production planning and control

  • Qualification:- B.TECH IT/CS/ECE/MCA/BCA/BSC.IT/DIPLOMA IT/B.TECH MECHANICAL/ELECTRICAL/B.TECH –CHEMICAL/DIPLOMA-CHEMICAL

  • BE / Diploma in Civil, with 8 - 15 Years of experience in land surveying, fluent use in the Land surveying equipment and should be proficient in handling compu Candidates who having Minimum 10 yrs of experience of which atleast 5yrs in hardcore sewerage pipeline networking project in middleast ...

  • Method Validation Development of analytical methods as per ICH guidelines Analytical Method transfers to manufacturing locations supervise & guide the scientist for trouble shooting Timely response of various queries from regulatory authority-USFDA M Pharma with USFDA/Europe & Developing Mkt in RA Good leadership and Managerial skills Should lead a group of 20+ RA / Scientist Exp in liquid injectables ...

  • We are opening for Maintenance Injectable. Should have major exposure in injectable only Should have exp in regulatory market US, EU. Should have exp in analytical development ...

  • USFDA, MHRA approved API plant. Will be leading a group of 50+ people which includes routine analysis, stability studies. Should have handson exposure on all instruements i.e. HPLC, GC, UV, IR etc. Will be reporting to site quality head

  • we have opening in QA in in injectable As Well as for OSD @ Multiple location should have face USFDA/MHRA. Qualification:- B.PHARMA/M.PHARMA/M.Sc

  • Manages a staff of professionals who setup regulatory information on raw materials, finished goods & author /maintain SDS& labels Coaches direct reports Manages budget May own one or more Product Safety work processes Project Management 10 years exp in Product Regulatory or Product Safety field 5 years exp with SDS & label authoring 3 years exp leading a team of professionals SAP exp Project ...

  • Should have an overall experience of at least 10 years in core manufacturing areas such as sheet metal, casting and/or plastics. Will lead Zuti’s initiative in product-process integration and facilitate prototype and manufacturing engineering development. In this role, will be responsible to co-ordinate DFM, DFA initiatives and mentor and develop engineers in these disciplines.ResponsibilitiesThe Team ...

  • Will undergo Zuti’s structured training and mentoring programme in CAE. As part of the training, will be trained in Finite Element (MBD/CFD) modelling and analysis tools and exposed to industry best practices. After successful completion of the training, will be assigned to project teams working under close supervision of expert team members working in functionally focused areas i.e., Durability, NVH ...

  • Should have experience of at least 3 years in Pro/ENGINEER and an overall experience of 6 years in the area of mechanical design. Will be the lead for independent projects and in the role will be responsible to co-ordinate with a team of design engineers to execute and deliver project work effectively.ResponsibilitiesThe Project Lead will be closely involved with project execution teams and take ...

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