Job as Project Coordinator, Executive at Medtronic

This is a question we’ve asked ourselves over and over. It’s how we at Medtronic have made hearts beat stronger and longer. It’s how we’ve pushed the limits of what technology can do in and for the body. It’s how we will continue to alleviate pain, restore health and extend life. Rising costs, an aging population, and the burden of chronic disease impact us all. And no single entity in the healthcare system can solve these challenges alone.

Post : Project Coordinator III/ Executive - Quality Assurance

Job Description
Responsible for establishment & implementation of robust Operations Quality compliance systems in Medtronic. Also responsible for ensuring that effective Quality Assurance systems, programs and processes are in place.

Key responsibilities :
• Maintain the Quality Management System (QMS) QA in compliance with Medtronic India (QMS) & ISO13485 standards.
• Responsible for implementation, handling and addressing routine Quality compliance systems and processes related to Corrective & preventive Actions (CAPA), BIS Registration, Change Management, Audit observations closure, Supplier Management, Training as per local regulatory requirements. Also, provides inputs towards their effective resolution in collaboration with relevant counterparts.
• Works directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet regulations.
• Execute process deliverables by interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance. Follow the guidelines set by corporate to Prepare quality procedures/reports related to QMS performance required for management review.
• Streamlining the process and follow-up (as required) quality training programs assigned to individuals across all applicable departments.
• Facilitates uniform standards worldwide and enables best practice sharing, thereby fostering the achievement of company's mission globally.
• Ensures all corrective action and preventive actions (CAPAs) or audit findings (if any) are completed on time for job area.
• Effective control of documents by proper distribution and archival in database.
• Establish & promotes a work environment that supports the quality policy and quality system.

Candidate Profile
• Must have at least 2 to 6 years relevant QA experience in the pharma/medical device/life science industry.
• Experience in Quality systems implementation and maintenance; GMP/Quality Systems Regulations; ISO 13485 is a plus.
• Easily communicate with colleagues, management and external authorities
• Be able to plan, manage, organize and report in an efficient way
• Be independent, persuasive, innovative and able to summarize
• Excellent verbal and written communication skills in English

Additional Information
Experience : 2-6 years
Qualification : M.Pharm, M.Sc, B.Pharm
Location : Gurgaon, Haryana, India
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Quality Assurance
End Date : 25th April, 2020