Oversee PLCM checklist management, ensuring accountability for obsolescence processes and Product Lifecycle transitions
Identify and drive SKU rationalization strategies by analyzing low-performing products based on margin, revenue, and volume
Serve as the primary liaison between cross-functional teams, Integrated Business Planning, and the PLCM group.
Partner with global teams, including Divisional DOLs, Planning COE, and PLCM leaders, to enhance and standardize planning processes.
Contribute to value improvement and design optimization activities.
What You need: Preferred experience (Strongly desired):
Understanding of Lean Manufacturing, Process Excellence/Six Sigma tools
Product Lifecycle & Disposition Management Hands-on experience in PLCM, obsolescence planning, product retirements, and supply chain impact analysis.
Change & Quality Management Expertise in ECN/ECR, CAPA, Non-Conformance (NC), and Quality Management Systems (QMS) in a regulated environment.
Regulatory & Compliance Knowledge Familiarity with FDA, EU MDR, ISO 13485 and experience managing design history files (DHF), risk management, and regulatory submissions.
Medical Device Design control and Sustenance activities experience preferred.
Strong communication skills in English, both written and verbal.
Minimum Qualifications (Required):
Bachelors/Masters in Mechanical, Electronics, or Mechatronics Engineering
8-11 years of relevant work experience
Travel Percentage: None
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