Presspart appoint Arun Sarda as Division Manager, Quality and Regulatory Affairs.
Presspart Manufacturing, the world’s leading provider of specialist metal and plastic metered-dose inhaler components to the pharmaceutical industry, is proud to announce and welcome Mr Arun Sarda as Division Manager for Quality and Regulatory Affairs.
Arun will be responsible for providing quality and regulatory support through the development and introduction of new pharmaceutical packaging and medical device products. Arun will also co-ordinate the integration of quality and regulatory requirements for new products into the relevant markets, supply chains and manufacturing locations
In conjunction with Presspart’s newly created Inhalation Product Technology Centre (IPTC), Arun will also be developing an enhanced regulatory guidance service for our customers and suppliers and site quality management teams
Arun joins Presspart having spent 5 years as Head of Regulatory Affairs and Quality for a sterile medical device manufacturer. Previous to this Arun spent 10 years holding various Quality and Regulatory Affairs positions within the Orthopaedics Industry working for Zimmer GmbH and Johnson & Johnson.
Mr David Biggs, Presspart’s Director for Global Quality & Regulatory Affairs commented “We are delighted to welcome Arun – his experience and knowledge will be a great asset to the Presspart team. As the global leader in the manufacture of metered-dose inhaler components it is essential that we are able to support not only our internal Quality requirements but also the requirements of our customers and supply chain. Arun will be a great addition to the team and I look forward to working with him”.