Your key responsibilities
In your role as Quality Change Management Specialist (f/m/d), you update databases and catalogues of product, manufacturing and regulatory compliance information according to the revision of procedures, specifications and forms.
You are responsible for preparing process and status reports, assigning and monitoring document numbers and reviewing documents for accuracy and completeness.
Within the Quality team, you will support to ensure the compliance to Change Control processes and therefore lead and execute the change control board review forums.
You liaise with relevant functional groups, facilitate and mentor teams through all stages of the change control process.
Acting as change analyst & approver, you have the responsibility for review and approval changes to processes and procedures, with attention to detail, review for completeness, accuracy and effectivity.
Additionally, you will participate and follow up to Stryker Internal, Corporate and third-party compliance audits.
What are we looking for?
Economical or Engineering degree or equivalent and a minimum of 2+ years of professional experience - preferred within a highly regulated industry.
You are characterized by a high level of commitment, service orientation and a solution-oriented, independent and structured way of working.
You are highly self-motivated and used to work independently with the ability to prioritize.
You hold excellent time management and organization skills, with high emphasis on attention to detail.
Your excellent English language skills enable you to collaborate with stakeholders across various functions and levels. German is also mandatory.
Contact: In case of questions regarding the position, please feel free to reach out to Sara Hendrickx via +49 761 4888 547.
Work From Home: Not available
Travel Percentage: Up to 25%