Supplier Quality Engineer

Fortive

  • Bangalore, Karnataka
  • Permanent
  • Full-time
  • 13 days ago
Your ImpactHere’s where you’ll demonstrate your competencies:
  • Will monitor quality performance of suppliers and external manufacturer’s and provide support in maintaining and reporting supplier quality metrics.
  • Will support in executing supplier change request activities and other routine supplier quality actions.
  • Support in the investigation of manufacturing product quality and compliance issues with assistance from appropriate SMEs and senior team members (e.g., CAPA, non-conformances, audit observations) Will support teams to investigate quality issues (Failure investigations) to resolve complaints, non-conforming products and CAPA.
  • Will provide support to maintain good documentation to support validation processes, specifications, manufacturing and test procedures.
  • Will participate and collaborate with Supply chain, R&D Engineering, Operations Engineering and other stakeholders to identify potential areas of process variability, address root causes and implement improvements.
  • Will be responsible for maintaining supplier information in purchasing system.
  • Will participate and support in process improvement activities.
  • Responsible for communicating business related issues or opportunities to next management level.
  • Performs other duties assigned as needed.
Our NeedsHere’s what we’ll need from you:
  • Bachelor’s Degree or above. Electrical Engineering (BSEE), Mechanical Engineering (BSME), Chemical Engineering (BSCE), BS Microbiology (BSc) or other related Engineering practices is required.
  • 2+ years of work experience (or equivalent) in the Medical Device industry, medical field or regulated environment, or in other applicable quality roles.
  • English communication skills required (read/ write)
  • Prior experience within an electro-mechanical or chemical environment as well as previous medical device experience is preferred.
  • Prior knowledge of medical device regulations such as 21 CFR 820 and ISO 13485 are preferred.
  • Must be able to work in a team environment, including frequent inter-organizational and outside customer contacts.
  • Must have good organizational skills.
  • Prior experience using electronic QMS software and SAP preferred.
  • Experience with Qualification and Process validations and the use/application of statistical tools is preferred.
  • Candidates who have prior experience in (sampling, design of experiments, process capability analysis) as well as the capability to review manufacturing processes (Control plan, process control and quality control) will be given higher considerations.
Fortive Corporation OverviewFortive’s essential technology makes the world stronger, safer, and smarter. We accelerate transformation across a broad range of applications including environmental, health and safety compliance, industrial condition monitoring, next-generation product design, and healthcare safety solutions.We are a global industrial technology innovator with a startup spirit. Our forward-looking companies lead the way in software-powered workflow solutions, data-driven intelligence, AI-powered automation, and other disruptive technologies. We’re a force for progress, working alongside our customers and partners to solve challenges on a global scale, from workplace safety in the most demanding conditions to groundbreaking sustainability solutions.We are a diverse team 18,000 strong, united by a dynamic, inclusive culture and energized by limitless learning and growth. We use the proven Fortive Business System (FBS) to accelerate our positive impact.At Fortive, we believe in you. We believe in your potential—your ability to learn, grow, and make a difference.At Fortive, we believe in us. We believe in the power of people working together to solve problems no one could solve alone.At Fortive, we believe in growth. We’re honest about what’s working and what isn’t, and we never stop improving and innovating.Fortive: For you, for us, for growth.Ready to move your career forward? Find out more at .Come join our team at Advanced Sterilization Products (ASP) and be part of a global leader in infection prevention solutions for the healthcare industry. With advanced products, technologies, and workflows for medical sterilization and disinfection, ASP is dedicated to defending the lives of patients, families, healthcare workers, providers, and communities. Add your talent to our extraordinary team and help us in our mission to make healthcare safer for everyone. ASP is based in Irvine, California with core sites in Everett, Washington and Schaffhausen, Switzerland plus many more offices around the world.

Fortive

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