QUALIFICATIONS:

• BS/BA, Master from a four-year college or university, preferably in a life science field of study

• +5 years’ experience in CE submissions for new medical devices and design changes on existing MDs (implants, IOLs, non-active, class I to class III)

• In-depth knowledge of MDD 93/42/EEC, global regulations, standards, and guidance documents

• Good understanding of general change impacts

• Logic thinking and understanding of authorities mindset/expectations

• Business sense, strategic thinking

• Very well organized and structured

• team member during development projects

• Ability to write easy to understand STED and other registration documents, rationales; well designed and organized, professionally presented.

• requires superb attention to detail

• Communicative with other departments, RA/CA team members cross-site and authorities

• MS Office software

• Project management skills

In a spacious modern setting full of opportunities for further development, ZEISS employees work in a place where expert knowledge and team spirit reign supreme. All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together.

Join us today. Inspire people tomorrow.

Diversity is a part of ZEISS. We look forward to receiving your application regardless of gender, nationality, ethnic and social origin, religion, philosophy of life, disability, age, sexual orientation or identity.