Manage end-to-end delivery of product lifecycle engineering projects, including scope, budgets, risks, deployments, communications, resource planning, and cross-functional coordination. Partner with marketing, quality, regulatory, and supply chain teams to ensure timely, compliant delivery of products and materials. Identify and mitigate risks, remove project obstacles, develop practical solutions, and lead cross-functional project teams in a regulated medical device environment.
The Project Manager will be responsible for end to end coordination and delivery of product lifecycle engineering projects. They will also support resource planning, budgets and implementing necessary processes to ensure function of the product lifecycle engineering team.
Let’s talk about Responsibilities
- Plan and coordinate scope, budget, risks, deployments and communications for product lifecycle engineering projects
- Interface with marketing, quality & regulatory and supply chain teams to ensure products, parts and materials are delivered on time and within specification and resolve technical issues as required.
- Provide a clear picture of risk across all activities and recommend areas to prioritize and how to address.
- Proactively identify and anticipate barriers. Assertively and creatively remove obstacles that slow down or prevent projects from delivering against defined objectives
- Consult and collaborate with managers and employees across the business to develop and implement workable project solutions.
- Lead and co-ordinate the activities of project cross-functional team (XFT)
- Maintains an awareness of industry trends, business conditions and internal processes and practices to influence the success of programs and initiatives.
Let’s talk about Qualifications and Experience
Required:
- Minimum 3-5 years’ professional experience within Med Tech or other regulated industries; or equivalent combination of education and experience
- Must have experience in Project Management tools and hands on experience in Project Management for R&D or Manufacturing projects
- Ability to communicate complex ideas effectively, both verbally and in writing
- Experience in understanding medical device development activities across a broad set of functions including quality and regulatory
- Exceptional analytical and quantitative problem-solving skills
- Ability to work collaboratively and effectively with people at all levels in an organization in a team environment.
#LI-APAC
Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you, apply now! We commit to respond to every applicant.
ResMed Singapore, Singapore, SGP Office
3 Tuas Ave 2 , Singapore, Singapore, 639443
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