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Senior regulatory affairs specialist (city of stirling)

Stirling
Medtronic
Posted: 6 October
Offer description

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

Overview

This position is an exciting opportunity to work with Medtronic's Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care.

Responsibilities

- Partner with local country RA affiliates to help planning, developing, and executing global regulatory activities necessary to obtain and maintain regulatory approvals in APAC region.
- Interact with local RA team within APAC region and provide support needed.
- Support and strengthen communication process between international RA and operating unit RA team.
- Support local RA team to prepare local submissions and obtain product approval/clearance, including assistance with government queries and registration documentation requirements.
- Review Change Orders and assess regulatory impact of product changes on international regulatory strategy and submissions per standard procedures.
- Participate and represent OUS regulatory function in sustaining (including MDR) and current product development projects to provide OUS regulatory requirements.
- Assist in keeping company informed of regulatory requirements in APAC region.
- Support product demand planning and release activities.
- Follow all assigned standard operating procedures and company policies to ensure compliance.
- Support all post-markets regulatory requirements and audit requests.
- Partner with local affiliates to help planning and executing license transfer and rebranding duties for the region.
- Other duties as assigned or required.

Required Knowledge and Experience

- Bachelor’s degree required with a minimum of 3-5 years of medical device regulatory affairs experience.
- Medical Device regulatory submission/approval experience.
- Knowledge of Asia Pacific regulations/requirements (e.g., TGA, PMDN, MFDS, TFDA, etc.).
- Strong interpersonal and analytical skills.
- Strong communication and technical writing skills.
- Attention to detail.

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.

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).

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.

Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart—putting ambitious ideas to work to generate real solutions for real people. From the R&D; lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here.

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📌 Senior Regulatory Affairs Specialist
🏢 Medtronic
📍 City of Stirling

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