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Documentation Specialist
Eingestellt von Berry Technical
Gesuchte Skills: Engineering, Product lifecycle management, Cad, Plm
Projektbeschreibung
Documentation Specialist
Solothurn, Switzerland
Contract - Until the end of 2013
70 CHF an hour
Our client is seeking an experienced Documentation Specialist to join their team on site in Solothurn.
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.
EDUCATIONAL REQUIREMENTS:
- Higher education
* Specific languages:
German - fluent
English - good
Experience:
Engineering knowledge
Medical Device - MUST
PLM Product Lifecycle Management
Doc Controlling - MUST
Please email.
Solothurn, Switzerland
Contract - Until the end of 2013
70 CHF an hour
Our client is seeking an experienced Documentation Specialist to join their team on site in Solothurn.
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.
EDUCATIONAL REQUIREMENTS:
- Higher education
* Specific languages:
German - fluent
English - good
Experience:
Engineering knowledge
Medical Device - MUST
PLM Product Lifecycle Management
Doc Controlling - MUST
Please email.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Medien/Design, Ingenieurwesen/Technik