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Document Controller - German Speaking - Solothurn, Switzerland
Eingestellt von Templeton and Partners
Gesuchte Skills: Controller, Engineering, Product lifecycle management, Plm
Projektbeschreibung
Document Controller - German Speaking - Solothurn, Switzerland
Mandatory skills:
Engineering knowledge
Medical Device experience
Document Controlling
PLM Product Lifecycle Management
Fluent in German and English
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.
Mandatory skills:
Engineering knowledge
Medical Device experience
Document Controlling
PLM Product Lifecycle Management
Fluent in German and English
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.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Organisation/Management