Title: Executive
Custom Field 2: 1973
Location:
Bavla, Gujarat, IN
Country/Region: IN
State: Guja
City: Bavla
Company: Dishman Carbogen Amcis Limited
Business Unit: General
Travel
Description:
- Planning of spares and consumables for better inventory and budgetary control as per approved norms.
- Cost effective and quality vendor development for engineering materials and services.
- To check purchase requisitions and contractor service bills.
- To prepare and review User requisition Specification (URS).
- Co - ordinate with consultant and vendors for different activates of project. Procurement and erection & commissioning activities for projects.
- To review project related documents (Design basis, layouts, P&ID's, GA drawings and control philosophy etc.) and ensure its implementation accordingly.
- To execute and monitor project activities and ensure quality.
- To review and ensure timely compliance of maintenance services to plant operation in coordinate with cross functional team like QA, QC, Production, Warehouse, Safety, HR, Finance and IT.
- Proper utilization of available manpower & manufacturing facilities for smooth operation of engineering activities.
- To ensure the optimization usage of resources for reduction in waste.
- To review and ensure the compliance of safety regulation and guidelines.
- Responsible for Green field and brownfield project concepts, plant designing, erection, commissioning & start-up of projects related to instrumentation.
- To ensure completion of preventive maintenance, calibration activities, validation activities and ensure timely compliance as per schedule.
- Checking of contractor's bills as per BOQ.
- Proper utilization of available manpower to expedite the maintenance and project activities.
- Execution and completion of maintenance and project work with respect to instrumentation.
- To ensure backup procedures are followed and backup of control system has taken by team member as per schedule.
- To review and ensure the compliance of cGMP documentation and regulatory documentation and proper record of the same.
- To prepare, review and update lists, training documents, master list, calibration planner, validation documents & other CGMP documents.
- Generation & review of history cards, organogram, job responsibilities, qualification / validation documents, layouts, P&IDs, Calibration, PLC/DCS Validation, written procedure including amendments / addendum if any.
- To Support & evaluate QMS activities (Like change controls, Deviations, Investigations, CAPA etc.
- Preparation and review of documents required for legal metrology, regulatory affairs etc & its compliance.
- Ensure online documentation related to all cGMP activities including data integrity.
- Preparation and execution of various planners / schedules.
- Strict adherence to safety, health and environment.
- Harmonization of GMP practices among all manufacturing blocks within the facility.
- To fulfil the current needs of training with respect to GMP, GLP, Safety & Hygiene, job, application etc.
- To provide training to team members as per requirement and ensure all team members completed their training as per CGMP requirement.
- Adhere to all the company policies & manuals (business, safety and finance etc.)
- Any other assignments allocated by reporting function(s).
Job Segment: Compliance, Facilities, Regulatory Affairs, Law, Warehouse, Legal, Operations, Manufacturing
