Job Description

For over 170 years, Leica Microsystems has helped shape the future by developing groundbreaking optical and digital solutions. As a global leader, we\xe2\x80\x99re driven by continuous improvement to excite our customers and to create the best work environment for our people. Customer focus, innovation, and teamwork are at the core of our culture and the foundation of our success.

Want to be part of a company whose products are part of cutting-edge research around the world? Join Leica Microsystems in our commitment for brilliant solutions and insight.

Leica Microsystems is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.

We currently offer the following position in our office in Singapore which will be hybrid with flexible office and home-office time. You will join an exciting and diverse Team of Regulatory, Quality and Clinical experts.

The Regulatory Affairs Senior Engineer is responsible for supporting the cross-functional teams in establishing and complying with Regulatory requirements for the assigned projects, medical devices (products) and geographical areas.

The role is also responsible for monitoring the evolving Regulatory world and respective changes, while keeping general maintenance of compliance of Leica\xe2\x80\x99s medical devices throughout their lifecycle.

In this role you work closely with Product Management, Marketing, R&D, Industrial Engineering, Scientific Affairs, Product Compliance and Manufacturing to define and execute regulatory strategies and deliverables that ensure timely regulatory clearance of newly developed Medical Devices as well as maintenance of registrations of medical devices that are already on the market.

YOUR RESPONSIBILITIES

Regulatory Projects

Supports and/or drives Regulatory initiatives.

Provides regulatory support for business initiatives on assigned specific projects

Evaluates the impact of new external requirements and works closely with relevant stakeholders to ensure compliance

Supports implementation of IT tools used in Regulatory Activities

Regulatory Affairs

Ensures regulations and standards monitoring

Defines regulatory strategy and requirements in support to new product introduction and lifecycle management projects

Creates and maintains Technical Documentation (EU MDR), US FDA submissions (e.g. 510(k))

Assesses impact of changes on product registrations world-wide

Supports creation and review of needed deliverables in accordance with the medical device development and change management processes

Maintains and supports international product registrations

Supports RAQA team with relevant regulatory deliverables in support of vigilance activities

Supports RAQA team in continuous improvement projects

OUR EXPECTATIONS

Degree from a technical college or university

Minimum 2 years of RA and/or QA experience in the medical device industry

Experience in leading continuous improvement projects in a matrix organization (ASQ, six sigma, lean certification would be a plus)

Experience in working with ISO 13485, MDD, MDR and FDA 21 CFR

English (mandatory), any other languages are considered a plus

WHAT WE OFFER

Attractive compensation package

Employees have the option to work from home up to 2 days/week

We offer flexible working time models - for us, New Work is more than just home office

We have no room for prejudices and stereotypes. We promote equal opportunities, diversity and inclusion. #Charterof Diversity

We offer a balance between support and autonomy to achieve your own goals in an international environment

With us you get the chance to successfully contribute your own ideas

At Leica Microsystems we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part of the time at the Company location identified above and part of the time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Leica Microsystems can provide.

GET MORE INSIGHT

Learn more about what we do and who we are by watching our company video \xe2\x80\x9cWe Are Leica\xe2\x80\x9d:

At Leica Microsystems we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Leica Microsystems can provide.

#LI-hybrid

When you join us, you\xe2\x80\x99ll also be joining Danaher\xe2\x80\x99s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you\xe2\x80\x99ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful tools and the stability of a tested organization.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

If you\xe2\x80\x99ve ever wondered what\xe2\x80\x99s within you, there\xe2\x80\x99s no better time to find out.

Danaher