jobs in LUXSHARE-ICT

LUXSHARE-ICT Hiring! Full Time Project Manager in - Ricebowl

Project Manager

LUXSHARE-ICT

Undisclosed

Singapore

Share
Save

Working Location

  • Singapore

Job Description

Responsibilities

About the Job

Luxshare is a global leader in advanced manufacturing and technology solutions, with a growing footprint in the medical device sector. As part of our strategic expansion, we are establishing a Singapore-based engineering hub to provide world-class medical device design and development services to clients across the global market.


We are seeking a Project Manager to plan, coordinate, and track individual medical device development and design-transfer projects from kickoff through completion. This role keeps cross-functional workstreams on schedule, on budget, and aligned to design control requirements.

You will work closely with engineering, quality, and operations leads to translate project plans into day-to-day execution, surfacing risks early and keeping stakeholders informed.


Key Responsibilities

  • Develop and maintain detailed project schedules, milestones, and resource plans for assigned development or design-transfer projects
  • Coordinate cross-functional teams (R&D, Quality, Operations, Procurement) to keep deliverables on track
  • Track project scope, timelines and budgets against plan, and flag deviations early
  • Prepare and distribute regular status reports, meeting minutes, and action item logs
  • Maintain project documentation in line with design control requirements (DHF inputs, meeting records, decision logs)
  • Support risk identification and maintain project-level risk and issue logs
  • Coordinate design reviews, phase-gate meetings, and project checkpoints
  • Assist with change control administration (ECO/ECN routing and tracking)
  • Escalate schedule, resource, or scope risks to Program Manager as needed
  • Support client status updates and meeting logistics under the direction of senior project staff
  • Any other duties as assigned by management


Key Requirements

  • Solid understanding of the medical device development lifecycle and design control basics.
  • Working knowledge of project scheduling and tracking tools (e.g., MS Project, Smartsheet)
  • Strong organizational skills and attention to detail
  • Clear written and verbal communication across cross-functional teams
  • Ability to manage multiple concurrent workstreams and shifting priorities
  • Strong analytical thinking with structured problem-solving capability
  • Strong influencing, communication, and stakeholder management skills across engineering, quality, regulatory, and operations functions
  • Professional working proficiency in Mandarin is a plus


Qualifications & Education

  • Bachelor’s or Master’s degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering or a related field
  • 4-6 years of experience in project management experience, ideally in medical device industry
  • PMP, CAPM, or equivalent project management certification


Project & Delivery Experience

  • Demonstrated success in supporting device products through the full design control lifecycle, from design input to commercial launch
  • Familiarity with tracking project scope, schedule and budget against baseline.
  • Proven leadership skills and ability to lead across global and cross-cultural teams.
  • Ability to develop and maintain strong cross-functional and external partnerships that deliver value to the overall business
  • Strong ability to collaborate with Manufacturing Teams to ensure prototypes are designed with manufacturability in mind and transition seamlessly into production.
  • Able to operate and priorities in a fast-paced and dynamic environment


Technical & Leadership Experience

  • Strong contribution to department strategy, resource and financial planning with focus on building scalable, entrepreneurial prototyping solutions that deliver business impact.
  • Able to translate project plan into clear, actionable tasks for team members
  • Communicate proactively with peers and stakeholders across global business units to report on progress, remove roadblocks and align strategies.
  • Knowledge of design control, risk management and DHF/DMR management under ISO 13485 and ISO 14971, including experience building or operating a QMS within a design services or contract engineering environment are preferred
  • Working knowledge of applicable IEC standards including IEC 60601, IEC 62304, and IEC 62366 (usability engineering), as well as biocompatibility requirements (ISO 10993) are preferred


Why Join Luxshare

  • Build hands-on project management experience within a growing medical device engineering hub
  • Work alongside experienced NPI, quality, and program leaders on real client programs
  • Be part of a fast-growing global organization with strong execution capability
  • Access to career growth, leadership opportunities, and international exposure


Additional Requirement

  • This role may require frequent travel to customers, suppliers, or manufacturing sites.


Important Information

Never provide your bank or credit card details when applying for jobs. Do not transfer any money or complete unrelated online surveys. If you see something suspicious, Report this Job ad.

Learn More