Sr Core Business Support Engineer II

work mode: hybrid

work location: sector 43, gurgaon

Summary

The Sr.Core Business Support Engineer II will lead and contribute to product and process change projects for existing Hollister products and processes in both our Ostomy Care and Critical Care businesses. The projects will be primarily related to Technical Transfer, Process Change , Material Change, Supply Security (stay in business), and Cost Savings. This is a permanent position based at the Gurugram facility.

RESPONSIBILTIES

• Live the Hollister Immutable principles, Develop test plans, analyze test data and interpret result
• Generate original ideas based on professional knowledge of product design for both ostomy and critical care products.
• Develop realistic action steps, timetables, and resource estimates for technical projects.
• Identifies potential challenges and proactively work to address them.
• Actively participate on cross-functional teams (international) and supports the completion of team deliverables.
• Validate plans within the team and acts on suggestions for improvement.
• Establishes a rapport with their working teams which allows them to identify key resources and network efficiently.
• Supports technical management in establishing goals and strategies.
• Communicate effectively and review project outcomes with internal customers.
• Completes written reports on technical activities carried out.
• Prepares and updates a range of technical documents including drawings and specifications.
• Provides technical support to Manufacturing, Engineering, Quality and Supply Chain.
  
  

• 8 to 12 years’ experience in a similar position, preferably in the medical devices sector
• Proven track record in project management and project leadership; capable of working independently
• Uses problem solving techniques such as DMAIC to resolve issues as they arise
• Demonstrates working knowledge of standard techniques, procedures, and criteria
  
  

• Strong communication skills, with ability to articulate relevant technologies and processes to others in the technical group and provide project updates to non-technical key stakeholders
• Solves technical issues using alternative or unique approaches
• Recognizes value-added product features and integrates them into product designs
• Demonstrates awareness of current technological trends, especially within their specific discipline
• Previous knowledge orexperience in field of Ostomy, Continence care would be added advantage (not mandatory)
• Previous knowledge or experience in polymer films, bonding technology would be added advantage (not mandatory)
• Ability to create, read, edit, and interpret 2D and 3D drawings as well as product specifications (with minimal oversight).
  
  

• Bachelor of Science / Engineering degree or higher preferably with Mathematics or Statistics as a subject
• PMP Certification is desirable (not essential)
  
  

• Experience with the FDA Quality Systems Regulations and an ISO 13485 environment at a medical device manufacturer (preferred)
• Project management training and experience (preferred)
• Experience with product development, design c ontrols, change controls and risk management for medical devices.
• Advanced statistics training and experience with plastic proicessing and/or automated assembly processes (nice to have)
  
  

• English
• Local Language
• Hybrid work environment with 3 days in the office and 2 days at home – performance based
• Two days per week will require flexible work hours to accommodate international project work with the USA and Europe