The position of Junior Quality Assurance Admin entails supporting the global Quality Organization at the Nobel Biocare headquarters in Zurich, Switzerland.
The position holder may support different roles and functions within the Quality Organization related to the Quality Management System, Document Management, Training and Education, Change Management, and Post-Market Surveillance.
ACCOUNTABILITIES
- review documents, in accordance with internal procedures and applicable regulatory requirements
- support process owners in the creation and update of procedures
- support Document Control activities
- support Change Management
- execute changes related to procedures and templates
- perform gap analysis
- support post-market surveillance activities
KNOWLEDGE, SKILLS & EXPERIENCE
- Higher education (bachelor's or master's degree).
- 1 Year of experience in the medical device industry or equivalent regulated industry (preferably in
- product development, quality management).
- Basic understanding and knowledge of medical device standards and regulations.
Critical Skills/technical know-how:
- The role holder must be able to act consequent and efficient, compliant and pragmatic.
- The role holder must be a quick learner related to the content of procedures.
- The role holder must be capable of working cross functionally and adapt quickly to the Nobel Biocare
- culture.
Critical Experience:
Experienced in interacting with stakeholders, cross-functional work and a basic understanding of relevant functions in the company.
CRITICAL SUCCESS FACTORS AND KEY CHALLENGES
- Customer orientation.
- Competence in medical device business.
- Ability to make self-reliant decisions considering the compliance risks.
Does it sound appealing to you? Send us your application, we look forward to having you on board!
The position of Junior Quality Assurance Admin entails supporting the global Quality Organization at the Nobel Biocare headquarters in Zurich, Switzerland.
The position holder may support different roles and functions within the Quality Organization related to the Quality Management System, Document Management, Training and Education, Change Management, and Post-Market Surveillance.
ACCOUNTABILITIES
- review documents, in accordance with internal procedures and applicable regulatory requirements
- support process owners in the creation and update of procedures
- support Document Control activities
- support Change Management
- execute changes related to procedures and templates
- perform gap analysis
- support post-market surveillance activities
KNOWLEDGE, SKILLS & EXPERIENCE
- Higher education (bachelor's or master's degree).
- 1 Year of experience in the medical device industry or equivalent regulated industry (preferably in
- product development, quality management).
- Basic understanding and knowledge of medical device standards and regulations.
Critical Skills/technical know-how:
- The role holder must be able to act consequent and efficient, compliant and pragmatic.
- The role holder must be a quick learner related to the content of procedures.
- The role holder must be capable of working cross functionally and adapt quickly to the Nobel Biocare
- culture.
Critical Experience:
Experienced in interacting with stakeholders, cross-functional work and a basic understanding of relevant functions in the company.
CRITICAL SUCCESS FACTORS AND KEY CHALLENGES
- Customer orientation.
- Competence in medical device business.
- Ability to make self-reliant decisions considering the compliance risks.
Does it sound appealing to you? Send us your application, we look forward to having you on board!