"Medopharm Private Limited" is a 54 year old company pioneer in the field of Pharma and We are expanding our plant and have the following openings in the Maintenance Department with experience in HVAC, plant machinery maintenance, electrical, plumbing, utility, and water plant maintenance for the Chennai, Guduvanchery location. Vacancy details:-HVAC - 2 Technician Plant Machinery Maintenance - 3 TechnicianUtility Maintenance - 4 TechnicianWater Plant System - 1 TechnicianInterested candidates can share your updated resume to career@medopharm.com

Roles and ResponsibilitiesEnsure compliance with statutory regulations, including Factories Act, MPCB rules, and other relevant laws.Conduct regular safety audits to identify hazards and implement corrective actions.Develop and maintain an effective Environmental Management System (EMS) to minimize environmental impact.Provide training on industrial safety, risk assessment, accident investigation, and occupational health best practices.Collaborate with cross-functional teams to develop policies and procedures for EHS management.Desired Candidate Profile4-6 years of experience in EHS management or related field.Strong knowledge of Ehs Compliance, Safety Audit, Safety Management, Industrial Safety, HSE Management, Occupational Health, Risk Assessment, Hazard Identification/Analysis.Experience with implementing ISO 45001:2018 OHSAS 18001:2007 standards.

Roles and Responsibilities Responsible for overall Quality System Review & ImprovementsHandling and control of Non-conforming products.Responsible for review & approval of key Quality System Procedures, Standard OperatingProcedures & other Master Documents.GAP Analysis of the process and products.Identifying the scope of improvement based on trend analysis.Putting forward the suggestions for improvements to the Management.Participation in audits, compliance and Tracking of Audit Compliances/Status.Review & closeout of Change Controls, Deviation Complaints & CAPA.Participating in Impact assessment, investigation & approval of deviations.Review & Approval of change controls, Deviations, OOS, CAPA, Market Complaints, etc.Ensuring implementation of software based QMS in the Organization.Ensure Compliance of Software based QMS Systems.Responsible for clearance of rejected Raw & Packing Materials.Desired Candidate Profile Candidate should have good communication skills and Pharmaceutical OSD Experience required