Sukhvinder Bal

Senior Manager Qa and Operations at Labomed Microsystems

Based in India

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Seniority

Manager

Department

Other

Location

India

Industry

Medical Equipment Manufacturing

Company size

42

Contact information

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Email

1 credit

s•••••••@laboamerica.com

Phone

5 credits

+91 ••• •••• ••••

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Background

About Sukhvinder Bal

An accomplished professional with 24 years of rich cross functional experience across the verticals of international Regulatory requirements, cGMP & QMS, customer support, product development, vendor development, inventory management, CNC Manufacturing and assembly operations in a optomechanical organisation of repute. Presently working with a well Known medical device manufacturing organisation engaged in designing, manufacturing and distribution of diagnostic devices for ophthalmic, gynaecology, neurosurgery, Dental and ENT applications Core Competencies Evolved. Expert in developing, implementing and leading manufacturing operations complying with USFDA, MDD, and ISO 13485 & ISO 9001 requirements right from scratch to certification. Proven ability in implementing JIT philosophy by using Lean tools of KANBAN, 5S & visual management in complex manufacturing environment including CNC manufacturing, conventional manufacturing, sheet metal operations, paint & anodizing. Successfully implemented cellular manufacturing in an optomechanical assembly line using two bin pull system to drive continuous improvement in quality and productivity and to reduce WIP. Proven abilities of enhancing production by optimizing resources and capacity utilization in a high precision CNC machining technology. Experienced in tool development of pressure die castings, gravity castings, plastic moulings and press work. An effective communicator with excellent relationship management skills. Strong analytical skills & problem solving abilities. Sound product knowledge and thorough understanding of product dynamics. Product & process Risk management specialist. ISO 13485 lead auditor. Management Representative. Expertise of handling US FDA inspections, 483s and warning letter issues. Time Management. Aggregate planning abilities.

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