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Supplier Quality Engineer

4.00 to 6.00 Years   Gurugram   28 Jun, 2021
Job LocationGurugram
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaQuality (QA-QC)
EmploymentTypeFull-time

Job Description

Be part of something altogether life-changingWorking at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.At Cytiva you will be able to continuously improve yourself and us working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity so you can grow your career and expand your skills in the long term.Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.We are seeking a Supplier Quality Engineer to ensure exceptional product quality for patient safety, customer value beyond expectations, regulatory assurance, and optimized cost of quality. You ll be part of a global team, leading the supplier management activities related to our Enterprise Solutions organization. Do you have a passion for Supplier Quality Then we would love to hear from you.What you ll do

  • You ll be collaborating with Engineering, Project Management, Business Development, and Sourcing teams on all activities required to effectively manage supplier quality requirements, supplier onboarding, and supplier development.
  • Own, plan and Manage qualifications of new suppliers/ product/ site (wing to wing responsibility) Primary areas of focus will be supplier qualification, part/process qualification, supplier auditing, issue resolution and improving supplier quality performance through continuous improvement activities and quality plan implementation.
  • Ensure supplier compliance to QMS and regulatory requirements through supplier monitoring process.
  • Collaborate with Suppliers and internal Partners to drive Quality improvements that minimize the Costs of Quality and support implementation of Supplier/Engineering Changes, New Product Introductions and Transfers.
  • Develop and execute Corrective and Preventive Action plans with suppliers to resolve non-conformance issues.
  • Build and implement Supplier Audit Plan and undertake supplier technical reviews when appropriate.
Who you are
  • Effective problem solver with the skills to lead Root Cause investigations / CAPA plans and influence others multi-functionally
  • Excellent communicator and collaborator who can influence at all levels of the organization
  • Experience in supplier technical development or supplier quality development
  • Qualified auditor experience preferably in both on-site and remote/virtual environments
  • Knowledge of quality critical aspects in industrial process control and how to verify and validate them through process qualification
  • Proven experience of Quality Management System tools (ISO9001, 2015), preferred ISO 13485 certification, continuous improvement methodologies, and site level products/processes; six sigma or Lean experience preferred
  • Experience in supplier quality engineering, quality assurance, quality engineering, manufacturing, or engineering; preferably in the biotech or pharmaceutical industries
  • Earned a Bachelor s degree in Engineering or technical field with experience in manufacturing, engineering or quality assurance
  • Proactive, results seeking and enthusiastic intensity
Commodities responsible for Heavy and light fabrication: Knowledge of ASME section IIX, WPS/ PQR, weld Map, NDT
  • Machining, process monitoring, process capability
  • Plastic and injection Molding
  • Casting, GDC, PDC, LPDC
  • Cable, PCBA
When you join us, you ll also be joining Danaher s global organization, where 68,000 people wake up every day determined to help our customers win. As an associate, you ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we ll empower you to push the boundaries of what s possible.If you ve ever wondered what s within you, there s no better time to find out. Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The EEO is the Law poster is available here . #LI-VK1When you join us, you ll also be joining Danaher s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System 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 ve ever wondered what s within you, there s no better time to find out.,

Keyskills :
danaher business systemiso 13485ppapproduct qualityquality management systemspcroot causeprocess controlsupplier quality engineeringpatient safetysix sigmaquality controlqualitycustomer value

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