JOB RESPONSIBILITIES 1. Overall responsibility of continual improvement and implementation of the organization's Quality Management System 2. Overall responsibility for facing 3rd-party regulatory audits, including CE audits (as per EUMDR), ISO 13485 audits, USFDA inspections, customer audits, etc. 3. To work as PRRC (Person responsible for regulatory compliance as per EUMDR. 4. Leading proper conduct and closure of Internal Quality Audits 5. Management of customer complaints & CAPA. 6. Management of Product-related documentation including Risk Management files, Pre-clinical Test reports, Clinical Evaluation reports, Usability Engineering files 7. Conducting required validations, in particular Sterilization Validation, Packaging Validation, Shelf-Life Studies/Stability Studies, Transportation Validation, etc. Preferred Candidate Profile ISO 13485 lead auditor training Location - Gurgaon (HR) & Baddi (HP) AT LEAST 8 years experience in CE-Certified disposable medical device company depth knowledge of ISO 13485 audits, EUMDR, USFDA inspections, customer audits.

Role & responsibilities 1. ABLE TO GENERATE NEW IDEA FOR AUTOMATION NEEDS. 2. PRACTICAL HANDS ON EXPERIENCE OF PNEUMATICS USED IN AUTOMATION. 3. AUTOMATION MACHINE ASSEMBLY AND TROUBLESHOOTING EXPERIENCE. 4. KNOWLEDGE OF LOGICS AND AUTOMATION PROGRAMMING. 5. CONVENTIONAL MACHINE WORKING EXPERIENCE AND KNOWLEDGE. Preferred candidate profile ITI, MECHANICAL DIPLOMA/MECHANICAL DEGREE WITH 7-12 YEARS EXPERIENCE IN AUTOMATION

Roles and Responsibilities Preparing the organization for, and facing EHS/ESG & CSR Audits including but not limited to: Sedex/SMETA, Ecovadis, customer audits etc. Preparing and maintaining SOPs and records for EHS activities including carbon reduction/greenhouse gas reduction plans Making, tracking and achieving targets for net-zero goals for the Organization; managing initiatives such as implementation of Solar Panel-based electricity generation, etc. Training employees on EHS activities/SOPs Assessing and improving Waste Management practices Assessing risk and possible safety hazards of all aspects of operations Focusing on prevention by keeping up with equipment maintenance and employee training Sharing information, suggestions, and observations with project leadership to create consistency in safety standards throughout the production team and the entire company Have Knowledge of ISO 14001 Environment Management System (EMS) and 45001 occupational health and safety (OH&S) management systems. Conduct regular environmental audits, risk assessments, and compliance checks. Coordinate environmental objectives, targets, and improvement programs. Ensure compliance with local, state environmental regulations. Monitor and manage data related to environmental performance (waste, emissions, energy use, etc.). Mock Drill: - Have knowledge to conduct the mock drills and maintain the corresponding documents. Fire Risk Assessment: Conduct comprehensive fire risk assessments to identify potential fire hazards in the workplace. Fire Safety Training: Organizing and delivering fire safety training programs for all staff members including educating employees on fire prevention measures, the proper use of fire fighting equipment, and evacuation procedures. Emergency Response Planning: Have knowledge of Developing and implementing effective emergency response plans specific to fire incidents. Fire Equipment Maintenance: Oversee the regular maintenance and inspection of fire fighting equipment, such as extinguishers, fire alarms, and sprinkler systems. Regulatory Compliance: Staying up-to-date with fire safety regulations and codes, and ensuring the organization complies with all relevant standards. Compliance: - Must have knowledge to handle the compliances w.r.t. Pollution control board, Fire Safety office etc. Desired Candidate Profile Bachelors/Masters Degree EXPERIENCE: At least 5 years in EHS/ESG & CSR field including experience with facing ESG/Social Accountability Audits Excellent written and oral English skills as required for preparing documents/facing audits from overseas auditors LOCATION: Gurgaon OR Baddi Advance safety Diploma/certificate from any recognized institute SALARY RANGE 7-12 lpa (55k -1 lakh/month) The company has two units as below: Unit-1: 110-111 Udyog Vihar Phase-4, Gurgaon, Haryana-122015 Unit-2: Saraj Majra Gujran, Suncity Road, Baddi, Distt. Solan, Himachal Pradesh - 173205 URL: www.harsoria.com

Role & responsibilities Responsible for managing all production activities, including planning, coordinating, and controlling manufacturing processes to ensure high-quality output and achievement of production targets Plan and execute weekly, monthly production schedules in alignment with business objectives. Reduce waste and improve efficiency using tools such as Time Study, Kaizen, 5S etc. Ensure optimal use of resources (materials, labor, equipment Ensure manufacturing processes comply with quality and regulatory requirements as per ISO 13485. Develop and foster cross-functional collaboration with engineering, quality and supply chain and PPC teams. Ensure adherence to safety standards and procedures. Responsible for Quality Control documentation as per our QMS requirement. Responsible to Lead and direct a team of 250 to 300 workforce and ensure efficient and effective production assembly operations. Preferred candidate profile Experience in Medical device manufacturing plant as Production AM/DM especially for Medical Tubing Products. Knowledge of Assembly product/components drawing reading. TOTAL EXPERIENCE: At least 8-10 years experience in a Medical device industry in Production department. Basic Knowledge about ISO 13485, GMP and Indian MDR.