Validation Manager Focus SAP Implementation

ZEISS Group
Jena, Germany
2 days ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English, German
Experience level
Senior

Job location

Jena, Germany

Tech stack

Business Process Model and Notation
Failure Mode Effects Analysis
SAP Applications
SAP HANA
SAP Implementation
System Testing

Job description

As Validation Manager Focus SAP Implementation (m/f/x) you are responsible for establishing, maintaining, and continuously developing an effective Quality Management System in compliance with applicable medical device regulations. The focus of the role is the coverage of Computerised System Validation (CSV) and the correct consideration of regulatrory requirements within the implementation phase of ZEISS FIT4 SAP S/4Hana Project., * You develop, maintain, and continuously improve the Quality Management System in accordance with ISO 13485, MDR, and other applicable regulatory requirements

  • You ensure the compliant implementation and application of MED QMS requirements within SAP-supported processes in cooperation with partner teams
  • You plan, drive, and document risk management activities across processes and projects
  • You develop, implement, monitor, and document validation strategies for Computerised System, ensuring compliance with regulatory requierments
  • You act as a subject matter expert and trusted advisor for quality and regulatory topics within cross-functional teams
  • You act as interface for in and -external Partners and support all activities regarding CSV

Requirements

  • You have a completed university degree (Master's level) in natural sciences, engineering, business administration, or a comparable qualification
  • You bring extensive years of professional experience in Quality Management within the medical device, pharmaceutical, or similarly regulated industry
  • You possess solid knowledge of quality management standards and regulatory frameworks, in particular ISO 13485, MDR, and 21 CFR Part 11 or comparable requirements
  • You have proven experience with Computerised System Validation (CSV)
  • You are familiar with quality methods and tools such as FMEA, CAPA, 5-Why, and risk management
  • You have valid experience with SAP and BPMN 2.0 is a plus
  • You demonstrate a structured and analytical approach and are able to interpret complex technical and business information
  • You work independently and in a solution-oriented manner with strong communication and organizational skills
  • You are fluent in English; German language skills are an advantage

About the company

ZEISS is technology, optics and innovation. We develop, manufacture and sell highly innovative products and solutions for our customers in a variety of business fields. As one of the world’s top technology companies with a portfolio aligned with future growth areas like digitalization, healthcare and Smart Production, and a strong brand to boot, ZEISS is shaping the future far beyond the optics and optoelectronics industries. The company’s significant, sustainable investments in research and development lay the foundation for the success, continued expansion and market leadership.

Apply for this position