Loading...
 
Share this Job

Semperit is a global rubber company with 5 different segments. With our quality products, we have been well positioned for almost 200 years and distribute them in more than 100 countries. This position belongs to our segment SEMPERMED, the last manufacturer of surgical gloves in Europe. Furthermore, we produce examination gloves for medical treatments and protective gloves for industrial applications. With almost 100 years of expertise only we offer the combination of unrivalled experience and ongoing research at a leading international level.  

Head of Quality and Regulatory Affairs Sempermed

Semperit is an internationally-oriented group that develops, produces and sells highly specialised rubber products with 5 different segments. With our quality products, we have been well positioned for almost 200 years and have distributions in more than 100 countries. This position belongs to our segment SEMPERMED, the last manufacturer of surgical gloves in Europe. Furthermore, we produce examination gloves for medical treatments and protective gloves for industrial applications. With 100 years of expertise, only we can offer the combination of unrivalled experience and ongoing research at a leading international level.

 

At our location in Wimpassing, Kamunting, Sopron, we are currently recruiting:

 

Head of Quality and Regulatory Affairs Sempermed 

 

 

Your tasks: 

  • You guarantee state-of-the-art quality processes along the entire value chain from raw material procurement to application in production
  • You will ensure that the regulatory requirements regarding market authorization as well as the continuous monitoring of the regulatory framework in the respective markets are met
  • The management of internal and external audits, management reviews and various quality reporting processes are also part of your responsibilities
  • You are Owner of the Quality management system and ensure appropriate QMS- and product- certification
  • You are responsible for the leadership and further development of the QM staff at the various locations
  • You will work closely with various departments regarding continuous improvement of quality processes
  • You will be responsible for leading the complaint handling process and managing activities with other departments regarding complaint management and the corrective actions derived from it

 

Your package:

  • Completed academic education or equivalent degree in science or engineering.
  • Leadership experience (in quality management) in an international environment
  • You already have good experience in the industrial areas of medical devices, pharmaceuticals, life science or chemistry
  • You have experience in operations and regulatory affairs
  • Good English skills – German is a plus

 

Gross monthly salary: from EUR 5.000- (according the collective agreement, full time); overpayment possible depending on professional qualifications and experience
 

Location: 2632 Wimpassing/Lower Austria (70km south of Vienna; company accommodation available on attractive terms) or any  other production site like Sopron (HU) or Kamunting (MY)

If you are interested, we request you to apply online.


Job Segment: Regulatory Affairs, Medical, Engineer, Law, Legal, Quality, Healthcare, Engineering