Healthium Medtech Limited
Rajesh Perumal Mathew has a diverse work experience in the field of marketing and communications. Rajesh Perumal is currently the Head of Marketing Communication & PR at Healthium Medtech Limited since 2022. Prior to this, they worked as a Business Advisor at Independent Management Consulting from 2019 to 2022, providing consultancy services on marketing, strategy, NPD, sales, and operations. From 2017 to 2019, Rajesh served as the Group Marketing Head [South Asia responsibilities] at MAS Brands India [MAS Holdings, Sri Lanka]. Rajesh Perumal also held the position of Vice President & Head [Marketing & Communication] at Muthoot Pappachan Group [Muthoot Fincorp] from 2014 to 2017. Rajesh's career started in 1995 as an Advertising Professional, working with well-known agencies such as Rediffusion DY&R, Wunderman Worldwide, Dentsu Communications, Ogilvy & Mather, Contract Advertising [JWT], Concept Oman, Lowe Lintas, and Saatchi & Saatchi. Throughout their career, they have held various senior management positions with P&L responsibilities.
Rajesh Perumal Mathew completed a Bachelor of Commerce (BCom) degree at Christ College | University, Bangalore.
Healthium Medtech Limited
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Healthium Medtech Limited is a global medical devices company focused on products used in surgical, post-surgical and chronic care. Fuelled by its vision to provide “Access to precision medtech for every patient, globally," it is present across 80 countries. 1 in 5 surgeries conducted globally, uses a Healthium product . As of Fiscal Year 2021, Healthium Medtech is the largest independent medical devices company in India and 2nd largest in the surgical consumables market, the largest non-captive surgical needles manufacturer globally by volume . Healthium is driving Innovation by focusing on R & D. Since fiscal year 2018, it has sold 30 new products. It holds 85+ patents (including pending applications) in U.S, Europe and India. It has 7 high precision, integrated manufacturing facilities with global certifications like US FDA, TGA, ISO and CE under the stringent new EUMDR norms.