• Responsible for the management of verification and validation tasks
• Involvement in the generation, reviewing, editing and reviewing of various protocols, FMEAs, test plans and summary reports
• Responsible for the generating, reviewing, editing and approving of SOPs, CAPAs and other applicable documentation
• Validation of software within the quality management system
• Supporting role for the change control proves of SOPs and other documents
• Leading role for cross-functional teams for qualification and validation activities within the organization

The ideal candidat

• Minimum a mechanical Bachelor´s Degree in a related field
• Relevant working experience in the field of medical device verification and validation of at least four years
• Experience in FDA/ GMP/ QSR /ISO13485 and within statistical techniques
• Leadership, interpersonal and strong decision-making skills
• Profound written and verbal communication skills
• Besides fluency in English, additional language skills are beneficial

We Offer

Professional and personal development within and developing international corporation. Are you the right candidate for this position?

I am looking forward to getting in touch with you.

Application process

• CV to my e-mail: m.burgstaller@sciproglobal.de
• Phone call with presentation of the company
• I will handle the contact person for the entire application process (Interviews until contract negotiations). You do not have to apply yourself
• Discuss additional exclusive posts tailored to you profile

My contact details at a glace

• E-mail: m.burgstaller@sciproglobal.de
• Tel: 089262058891
• Xing: https://www.xing.com/profile/Michael_Burgstaller19/cv
• LinkedIn: https://www.linkedin.com/in/michael-burgstaller-0790b7136/