Related content
Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
Who we want:
· Collaborators. Partners who listen, share thoughts, and work together to build and leverage relationships in order to meet project goals.
· Problem solvers. Critical thinkers who are motivated to solve challenging problems.
· Dedicated achievers. Those who aspire for excellence in a fast-paced environment and take ownership of their work.
· Curious learners. People who seek out cutting-edge research and information to expand and enhance their ability to develop new ideas into reality.
· Customer-focused. Engineers who can partner with our customer to drive purposeful innovation, resulting in best-in-class products.
What You will do:
Key Responsibilities
- Ensuring compliance to Supplier Control activities identified by organization.
- Experience of PPAP associated with New Product Launches and Management of Production cycles there after (Manufacturing Transfers).
- Participate in cross- functional teams in the development of new products or changes related to current products in meeting customer requirements.
- Applies sound, systematic problem-solving methodologies (5Why, DMAIC, 8D, C&E) in identifying, prioritizing, communicating, and resolving quality issues - NC & CAPA to facilitate root cause analysis and corrective actions of supplier quality issues.
- Promote the use of continuous improvement methodologies such as Lean, Six Sigma, Poka- Yoke (Error Proofing), Measurement System Analysis (MSA), Statistical process control (SPC) and Process Failure Mode and Effects Analysis (pFMEA)
- Evaluate Quality data to identify process improvement opportunities within the supply chain.
- Coordinate Change Management & Control with Suppliers and implement changes at Supplier.
- Review of process and equipment Validation including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Special Process Validations, and Test Method Validations.
- Inspecting and testing materials, equipment, processes, and products to ensure quality specifications are met.
- Prioritizing, reviewing, and delivering First Article Inspections FAIs for sustaining parts and development projects.
What You Need:
Must have Skills
- B.Tech (Electronics/Electrical/Mechanical) with 2-5 years of experience in Quality / Engineering / Manufacturing environment.
- Quality Processes/ Tools - Working knowledge of basic and advanced Quality tools such as; PPAP, Six Sigma, SPC, FMEA, Control Plans, Root Cause Analysis, Poke Yoke, Kaizen, Lean Manufacturing etc.
- Executes/implements/ improve all supplier quality tools/ Processes. Trains supplier in these tools effectively.
- Proficient in MS Office Suite (including Word, Excel, Power Point etc).
- Strong interpersonal skills to work with cross-functional teams (engineering, R&D, manufacturing, regulatory affairs).
Good to have Skills:
- Understanding of Medical Device Regulatory Compliance (ISO 13485, CFR 820, or comparable standard / regulation) and EU's Medical Device Directive.
- Excellent communication and influencing skills, with the ability to manage multiple tasks and represent the Quality function across teams
- Preferred ASQ Certified Quality Engineer (CQE).
- Commodity Domain Knowledge – Strong Knowledge & understands technology, regulatory requirement related to product, system & services.