drjobs Staff Specialist, Labeling and Technical Publications

Staff Specialist, Labeling and Technical Publications

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1 Vacancy
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Job Location drjobs

Gurgaon - India

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Work Flexibility: Hybrid or Onsite

What you will do:

  • Review & approval co-ordination of labeling jobs. Main tools are Microsoft Teams Planner and onePLM

  • Translation coordination of labeling and regulatory documentation professional communication with external vendors

  • Publication and/or uploading of approved documents on global portalsSupporting labelling system for periodic updates & reports

  • Print current labels for Regulatory Authority registration requests & Support with printing current/updated labels during mass changes

  • Represent Global Labeling as Local Project Coordinator on major projectsProcess and implement labeling related change requests (ECR/ECN) support with the coordination of ECR related activities.

  • Support Labeling updates/revisions graphic design including stakeholder management Utilize and comply with Strykers Quality Management System including proactively verifying if requirements are met and managing changes within the Quality System

  • Reviewquality assurance documentation to support mainlyproduct sustenanceand product life cycle management.

  • Support risk management activities for Sustenance projects - Ensure that risk measures are conducted in accordance with State-of-the-Art requirements and are implemented correctly into the labeling.

  • Taking care of timely and quality deliverables for assigned projects.Work as point of contact for all people related aspects with the stakeholders and review meetings with the team to monitor progress of projects and provide guidance develop contingent plans and arrange resources as needed.

What you need:

  • Strong Work experience: 7-10 years out of which 5 years experience indesigning writing and publishing technical documentation (labelling/technical publication/collateral materials) and/or Design Quality Assurance) or new product development (medical devices)

  • Knowledge of EU MDR changes ISO 14971 IEC 62366 Quality Concepts (e.g. CAPA Audits Statistics) preferred

  • Must possess strong project management skills as well as can manage multiple tasks simultaneously Demonstrated ability to advocate for product excellence and quality.

  • Ability to brainstorm potential solutions and execute acc. to plan

  • Knowledge in systems and databases preferred onePLM (CAII ideal) sharepoints and online applications

  • A relevant bachelors degree (science/engineering)

  • Excellent verbal and written communications. Great organization capability to follow a given plan

Travel Percentage: 10%


Required Experience:

Staff IC

Employment Type

Full-Time

Company Industry

Key Skills

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