You are successfully logged out of your my randstad account

You have successfully deleted your account

qms project support.

Job Details

zusammenfassung.

Beschleunige die Bewerbung, indem du dein Profil teilst

Job Details

Our client, based in Lucerne, is looking for a QMS Project Support for a 1 year contract.


General Information
 

• Start date: 3.01.2023

• Workload: 100%

• On-site/Home Office: On-site is required



Primary Responsibilities include:
 

  • Key collaborator working closely with site personnel and Clinical Supply QMS Redesign Team to ensure successful implementation of new QMS by assisting with project-specific tasks, including but not limited to, project management, document management, documentation review, technical editing, meeting coordination and facilitation, training, onboarding, and other administrative tasks.

Specific tasks may include:
  • Work on Complaint Investigations
  • Perform documentation review and technical editing to ensure consistency (e.g. language, formatting, etc.) within the Redesign Team and across the Clinical Supply network
  • Serve as communication channel between global network site personnel
  • Assist with site metrics collection / reporting and sharing of success stories / achievements
  • Support development of the learning strategy for new and revised QMS topics, including access to LMS content and generation of reports, creation of training materials and communication of training requirements
  • Being responsible for project management activities, optimization of communication strategy and change management strategy
  • Management of document lifecycle (new or existing documents) and review/approval workflows
  • Maintain electronic repository / communication mechanism (e.g. QMS SharePoint Site, Microsoft Teams)
  • Serve as a change agent helping the Clinical Supply QMS Redesign Team drive culture change


Required Education and Skills:
 
  • Bachelor’s Degree in an appropriate scientific or business field of study or longtime education in this area
  • Minimum of five (3-5) years’ experience in the Pharmaceutical or equivalent industry
  • Strong technical knowledge, skills and experience in project and documentation management


Preferred Education and Skills:
 
  • Excellent verbal and written communication skills as well as presentation skills
  • Strongly developed cross-functional teamwork and collaboration skills
  • Experience in Microsoft tools such as Outlook, Word, Excel, PowerPoint, SharePoint, Teams and Project is strongly recommended
  • Experience with document editing in MS word (e.g. formatting, forms, styles, templates, etc.)
  • Experience directly related to the development of Quality Standards and core requirements for Market Supply and / or Clinical Supply
  • Experience directly related to Quality Assurance, Quality Control, GMP regulations or pharmaceutical regulations
  • Knowledge of processing mapping and optimization
  • Language English C1 and German B2, written and spoken

Our client, based in Lucerne, is looking for a QMS Project Support for a 1 year contract.


General Information
 

• Start date: 3.01.2023

• Workload: 100%

• On-site/Home Office: On-site is required



Primary Responsibilities include:
 

  • Key collaborator working closely with site personnel and Clinical Supply QMS Redesign Team to ensure successful implementation of new QMS by assisting with project-specific tasks, including but not limited to, project management, document management, documentation review, technical editing, meeting coordination and facilitation, training, onboarding, and other administrative tasks.

Specific tasks may include:
  • Work on Complaint Investigations
  • Perform documentation review and technical editing to ensure consistency (e.g. language, formatting, etc.) within the Redesign Team and across the Clinical Supply network
  • Serve as communication channel between global network site personnel
  • Assist with site metrics collection / reporting and sharing of success stories / achievements
  • Support development of the learning strategy for new and revised QMS topics, including access to LMS content and generation of reports, creation of training materials and communication of training requirements
  • Being responsible for project management activities, optimization of communication strategy and change management strategy
  • Management of document lifecycle (new or existing documents) and review/approval workflows
  • Maintain electronic repository / communication mechanism (e.g. QMS SharePoint Site, Microsoft Teams)
  • Serve as a change agent helping the Clinical Supply QMS Redesign Team drive culture change


Required Education and Skills:
 
  • Bachelor’s Degree in an appropriate scientific or business field of study or longtime education in this area
  • Minimum of five (3-5) years’ experience in the Pharmaceutical or equivalent industry
  • Strong technical knowledge, skills and experience in project and documentation management


Preferred Education and Skills:
 
  • Excellent verbal and written communication skills as well as presentation skills
  • Strongly developed cross-functional teamwork and collaboration skills
  • Experience in Microsoft tools such as Outlook, Word, Excel, PowerPoint, SharePoint, Teams and Project is strongly recommended
  • Experience with document editing in MS word (e.g. formatting, forms, styles, templates, etc.)
  • Experience directly related to the development of Quality Standards and core requirements for Market Supply and / or Clinical Supply
  • Experience directly related to Quality Assurance, Quality Control, GMP regulations or pharmaceutical regulations
  • Knowledge of processing mapping and optimization
  • Language English C1 and German B2, written and spoken

kontaktiere uns.

wir sind da um deine Fragen zu beantworten.

AB

Audrey Bisch

Danke für die Anmeldung zu persönlichen Job-Benachrichtigungen.