Assoc MDR/Vigilance Spec

Medtronic•13h ago

Hyderabad, Andhra Pradesh, IndiaOnsiteFull-timeEntry Level1+ yrs exp

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Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health
extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth
impact. A Day in the Life Job Responsibilities
Evaluates incoming complaint information and maintains the record in the electronic database.
Performs follow up activities to obtain additional information. Use and maintain database(s), provide analysis and trending data all on complaints.
Determines Reportability of complaints to Government Agencies.
Identify and document appropriate complaint categories to assure trend accuracy within the complaint database.
Writes investigation summaries based on technical product analysis information provided;
Ensures record documentation is maintained in a constant state of audit readiness per internal policies.
Liaison with groups who perform additional investigation and who prepare written record of investigation.
Interact with Technical Service, Manufacturing, R&D, and Quality Assurance, as needed, during the course of complaint processing.
Provide basic technical expertise and assistance in handling complaints to comply with current FDA and International reporting regulations.
Reviews and interprets risk management documentation as it applies to the complaint event.
Interacts with multiple departments within Medtronic - MITG, such as Technical Services, Failure Investigation, R & D, Manufacturing and Engineering.
Interacts with groups external to Medtronic - MITG, such as customers, vendors, health care professional Minimum Qualifications
Bachelor degree; Engineering or Science degrees preferred (e.g.EE, ME, Biomedical Engineering)
1 to 3 years quality assurance or regulatory experience in medical or pharmaceutical industry.
Computer literate with skills in Word, Excel, Access, PowerPoint and database trending analysis
Strong typing skills and ability to write business documents with minimal supervision.
Strong verbal and written communication skills and ability to work in a team oriented environment
Ability to multitask.
Ability to understand the functionality / intended use of complex medical devices.
Minimum travel may be required Nice to Haves
Knowledge of medical devices, their development and quality control.
Knowledge of FDA, MEDDEV, Canadian Regulations.
Technical Writing experience. About Medtronic Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives.Help us shape the future. Whatever your specialty or ambitions, you can make a difference at Medtronic - both in the lives of others and your career. Join us in our commitment to take healthcare Further, Together. Job Responsibilities · Evaluates incoming complaint information and maintains the record in the electronic database. · Performs follow up activities to obtain additional information. Use and maintain database(s), provide analysis and trending data all on complaints. · Determines Reportability of complaints to Government Agencies. · Identify and document appropriate complaint categories to assure trend accuracy within the complaint database. · Writes investigation summaries based on technical product analysis information provided
· Ensures record documentation is maintained in a constant state of audit readiness per internal policies. · Liaison with groups who perform additional investigation and who prepare written record of investigation. · Interact with Technical Service, Manufacturing, R&D, and Quality Assurance, as needed, during the course of complaint processing. · Provide basic technical expertise and assistance in handling complaints to comply with current FDA and International reporting regulations. · Reviews and interprets risk management documentation as it applies to the complaint event. · Interacts with multiple departments within Medtronic - MITG, such as Technical Services, Failure Investigation, R & D, Manufacturing and Engineering. · Interacts with groups external to Medtronic - MITG, such as customers, vendors, health care professional Minimum Qualifications · Bachelor degree
Engineering or Science degrees preferred (e.g.EE, ME, Biomedical Engineering) · 1 to 3 years quality assurance or regulatory experience in medical or pharmaceutical industry. · Computer literate with skills in Word, Excel, Access, PowerPoint and database trending analysis · Strong typing skills and ability to write business documents with minimal supervision. · Strong verbal and written communication skills and ability to work in a team oriented environment · Ability to multitask. · Ability to understand the functionality / intended use of complex medical devices. · Minimum travel may be required Nice to Haves · Knowledge of medical devices, their development and quality control. · Knowledge of FDA, MEDDEV, Canadian Regulations. · Technical Writing experience. About Medtronic Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives.Help us shape the future. Whatever your specialty or ambitions, you can make a difference at Medtronic - both in the lives of others and your career. Join us in our commitment to take healthcare Further, Together. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. Recruitment Fraud Alert We are aware of phishing scams targeting job seekers. Please keep the following in mind: Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate. If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments. If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com . Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

Required skills

Quality AssuranceRegulatoryMedical DevicesTechnical WritingWordExcelAccessPowerPointDatabase Analysis