Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Technical Writer - Pharma Experience - Long term Contract - 90%
Eingestellt von Edelway
Gesuchte Skills: Support, Design
Projektbeschreibung
Our multinational end client is now looking for a technical writer to join its team.
We can offer a 6 months contract at 90% renewable on a long term basis.
RATE: 90 - 95 CHF/hour.
All hours will be paid. We take care of all the administration and payroll.
Start date: ASAP
THE ROLE:
*The Technical Writer role is focused on creating, assimilating, and conveying technical material in a concise and effective manner.
*Experience in ITILv3 best practice required.
YOU WILL:
*Create, assimilate, and convey technical material in a concise and effective manner.
*Create and develop manuals and SOP's to support IT operations.
*Assist in planning, creating and developing various operation/maintenance manuals, training materials, instruction guides and other technical documentations related to IT operations.
*Participate in process design meetings with relevant SMEs (Subject Matter Experts).
*Gather all relevant process and support information from relevant SMEs.
*Incorporate all information into required process definition documents, support policies, work instructions, user documents, training guides, and other relevant documents.
*Assimilate knowledge during discovery and collaborate with senior management to assess current processes and define/document improvements in line with ITIL v3 standard.
*Assist in identification of discrepancies/gaps in current processes and deliverables.
*Review and edit technical writing by other team members to maintain clarity, consistency, and quality.
*Deliver final versions of the materials and submit to document control for release.
*Maintain project and task plans and assignments.
*Adhere to all departmental policies, procedures, standards, and document templates where applicable.
YOUR PROFILE:
*Technical writer with experience in ITILv3 best practice.
*Fluent in English (oral and written). German would be a plus
*Excellent in technical English.
*Excellent technical documentation skills.
*5+ years previous experience in writing technical documentation for complex software systems and service management.
*Pharma experience together with a good understanding of processes/organization etc. is a true asset.
*Good understanding of GxP and 21CFR part 11 requirements, preferably in Pharma Industry.
*Experience with MS Office Tools, MS SharePoint and MS Project.
*Team work in a challenging IT environment.
*Ability to work in an international as well as multicultural environment.
*Good verbal communication skills.
*Ability to translate complex concepts into user-friendly, clear, concise information for the end user.
*Good illustration skills.
*Flexibility and experience in prioritizing tasks.
*Ability to deal with variable workload.
*Ability to achieve goals and resolve issues.
If this sounds like your next challenge send us your CV and we will contact you to discuss it in more details.
We can offer a 6 months contract at 90% renewable on a long term basis.
RATE: 90 - 95 CHF/hour.
All hours will be paid. We take care of all the administration and payroll.
Start date: ASAP
THE ROLE:
*The Technical Writer role is focused on creating, assimilating, and conveying technical material in a concise and effective manner.
*Experience in ITILv3 best practice required.
YOU WILL:
*Create, assimilate, and convey technical material in a concise and effective manner.
*Create and develop manuals and SOP's to support IT operations.
*Assist in planning, creating and developing various operation/maintenance manuals, training materials, instruction guides and other technical documentations related to IT operations.
*Participate in process design meetings with relevant SMEs (Subject Matter Experts).
*Gather all relevant process and support information from relevant SMEs.
*Incorporate all information into required process definition documents, support policies, work instructions, user documents, training guides, and other relevant documents.
*Assimilate knowledge during discovery and collaborate with senior management to assess current processes and define/document improvements in line with ITIL v3 standard.
*Assist in identification of discrepancies/gaps in current processes and deliverables.
*Review and edit technical writing by other team members to maintain clarity, consistency, and quality.
*Deliver final versions of the materials and submit to document control for release.
*Maintain project and task plans and assignments.
*Adhere to all departmental policies, procedures, standards, and document templates where applicable.
YOUR PROFILE:
*Technical writer with experience in ITILv3 best practice.
*Fluent in English (oral and written). German would be a plus
*Excellent in technical English.
*Excellent technical documentation skills.
*5+ years previous experience in writing technical documentation for complex software systems and service management.
*Pharma experience together with a good understanding of processes/organization etc. is a true asset.
*Good understanding of GxP and 21CFR part 11 requirements, preferably in Pharma Industry.
*Experience with MS Office Tools, MS SharePoint and MS Project.
*Team work in a challenging IT environment.
*Ability to work in an international as well as multicultural environment.
*Good verbal communication skills.
*Ability to translate complex concepts into user-friendly, clear, concise information for the end user.
*Good illustration skills.
*Flexibility and experience in prioritizing tasks.
*Ability to deal with variable workload.
*Ability to achieve goals and resolve issues.
If this sounds like your next challenge send us your CV and we will contact you to discuss it in more details.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Medien/Design, Sonstiges