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Our client is a leading international producer of high-quality products within the medical technology industry, representing a highly regarded brand worldwide.

 

For the construction of a new plant, planned to get productive within the next two years, we ae currently seeking an

 

Interim Manager QA – Validation Engineer MedTec (f/m)

 

Responsibilities

  • Supports the execution of the equipment qualifications for all global technology projects and process

  • improvements

  • Ensures that all clients guidelines (e.g. IMSU, EHS) and as well as all national laws are applied in the projects in case of qualification

  • Supports the production sites worldwide in case of qualification for equipment’s and/or processes if requested

  • Supports the execution of the process validation if required from internal customers

  • Supports the continuous improvement of the qualification process and documents for pharmaceutical equipment regarding the GMP / cGMP guidelines

  • Supports a professional platform with interaction of Pharmaceutical Systems internal departments as well as other client departments and third-party professionals

  • Leads Qualification sub-projects and/or Qualification-work packages for technology projects

  • Ensures adherence to and monitoring of legal laws and internal regulations concerning IMSU / EHS / cGMP / Guidelines for pharmaceutical supplier industry / Safety regulations in his/her organization and occasionally involved in the development of new concepts and directives in close cooperation with the IMSU / EHS team and external certified bodies.

  • Ensures implementation of the concepts in his/her area of responsibility and takes care of the corresponding instruction and training of his/her employees

 

Requirements

  • Degree in Engineering, Production Technology, MBA

  • 5 Years of experience engineering and qualification of pharmaceutical equipment in a global environment and in intercultural project teams, thereof at least 3 years with the responsibility for qualification for pharmaceutical equipment.

  • Experience in multi project management.

  • Strong qualification capability regarding the cGMP and GAMP guidelines

  • Structured and methodical working style (e.g. FMEA, SWOT, TCO)

  • Excellent oral and written communication, negotiation, documentation and cross-functional management skills.

 

Language skills

  • Business fluent command of English

  • German advantageous

 

Offer

Start: Q1 2019

End: End of 2020

Workload: 100%

Location: Switzerland, South Germany

 

We offer a very challenging Interim Management position with plenty of room for growth. Sign up over Stefan Ehrlich Head Business Development; by mail stefan.ehrlich@swiss-interim-management.ch / Phone +41 44 5853971 or online registration.

Job details

Location Switzerland / South Germany
Type Interim Management
Start Date Q1 2019
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