Beschreibung
OVERALL RESPONSIBILITIES:* Change Request (CDR/DCO/ECR) processing and final release
o Assure documentation format/template standards and requirements are maintained
o DCO coordination, approval eSignature validation, release activities
o Final release verification and notifications
* Document Number Issuance
* Assist with cross-workstream inter-document impact assessments
* ICDS request logging, tracking and verification
* Communicate/coordinate cross-workstream documentation processing
POSITION DUTIES & RESPONSIBILITIES:
* Process change requests and document updates in a timely manner
* General clerical duties, including document scanning, data entry, filing, and email.
* Additional duties as assigned.
* Know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times.
* Diligently participate in our compliance program-related activities as denoted by your supervisor or our Chief Compliance Officer.
PROFESSIONAL EXPERIENCE REQUIREMENTS:
* Experience with document control / management systems and quality requirements in the medical device or other regulated industries is strongly preferred.
* High level of proficiency in MS Word and Excel. Experience in Adobe Professional, Visio, CAD software is a plus.
* Demonstrated excellent written and verbal communication skills.
* Specific languages: German - fluent, English - good
If you feel suitable for this position I am looking forward to receiving your online application.
To find out more about Real please visit www.realstaffing.com