Experience in new projects / project expansions of existing facilities
involving from conceptual study to various phases of project like basic engineering, detail engineering, pre-commissioning / commissioning of equipment.
Responsible for preparation of various regulatory inspections/audits and need based active participation during audits
workload forecasting and ensuring effective work processes& procedures are in place and are being followed / used by all the team members.
co-ordination with cross functional teams and with the vendors to manage the project time to time.
Experience in developing Block Flow Diagrams, Process Flow Diagrams, Piping and instrumentation Diagrams, Mass and utility balances, safety analysis etc
Should have hands on experience in conceptual, detailed design, project planning, execution and qualification
Should have hands on experience with process valve matrix, process sequence logics, functional design specification ( FDS), process control sequences, CIP/SIP sequences etc...
Working experience in reviewing/development of URS, Tendering, preparation of technical comparisons, DQ, FAT, recipient of equipment, SAT, commissioning, qualification and closeout of Biopharmaceutical facilities.
Ability to work in a team structure- plan organize and prioritise work
Ability to analyse quantitative data, create and/or edit written reports and be able to process information.
High level of working proficiency in AutoCAD & MS Projects