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Location
In office (Singapore)
Seniority
Middle · 3+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 5, 2026. First seen by Alion on Nov 2, 2026. ResMed scores B on the Alion truth index.

Overview
Company
Impact
Profile match
ResMed is a medical device company founded in Sydney in 1989 by a physician who had helped develop the first practical treatment for obstructive sleep apnoea and could not persuade anyone else to commercialise it. It makes the masks, flow generators and ventilators used to treat sleep apnoea and chronic respiratory disease, and it has built a large software business in the cloud platforms that manage those devices and the out-of-hospital care around them. Now headquartered in San Diego and listed in New York and Sydney, it shares the sleep apnoea market largely with Philips and benefited substantially from its competitor's device recall.
Backed by Hikma Ventures

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.

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.

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