Quality Management Officer*in at vara

Intro

As the Quality Management Officer, you will be responsible for developing and executing strategies on a global scale to develop and maintain the quality management system (QMS) in compliance with ISO 13485.

Tasks

Develop and maintain the quality management system (QMS) in compliance with ISO 13485.
Ensure safety and compliance of QMS processes as the Person responsible for Regulatory Compliance.
Provide training and support to staff on QMS processes, regulatory requirements, and best practices.
Manage internal and external audits to ensure compliance with regulatory requirements.
Drive continuous improvement initiatives within the organization.
Act as the in-house quality expert, advising and supporting internal and external stakeholders.
Collaborate with cross-functional teams to ensure regulatory and quality compliance throughout the product lifecycle.

Requirements

Bachelor’s degree or higher in a relevant field (e.g., Engineering, Life Sciences, Quality Management).
Minimum of 3 years of experience in the management of QMS within the medical device industry.
Extensive knowledge of quality management systems, and especially ISO 13485 requirements.
Excellent communication, negotiation, and interpersonal skills.
Strategic thinking and problem-solving abilities.
High attention to detail and accuracy.
Flexibility and adaptability to work in a fast-paced, dynamic environment with changing market conditions.
Fluent English, German highly desired.

Benefits

Flexible work arrangements (in-office, remote, or hybrid).
Regular team nights and events to foster company culture.
Access to the AI campus with opportunities to meet inspiring startups and events.
Competitive salary benchmarked within the tech and healthcare industry.
Career development sessions with your manager.