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This position is responsible for the creation and processing of all change request packets, creation of controlled documents, tracking of packets and all associated paperwork involved. This requires participation as an active team member in cross functional teams and ownership of project team documentation. Responsibilities also include the origination, editing and revision of technical documentation. This position will also assist with the migration between two different MasterControl systems.
Job Responsibility:
Creation and processing of all change request packets
Creation of controlled documents
Tracking of packets and all associated paperwork
Participation as an active team member in cross functional teams and ownership of project team documentation
Origination, editing and revision of technical documentation
Assist with the migration between two different MasterControl systems
Participates in regulatory compliance audits and inspections
Participates in investigations
Completes applicable job-specific training
Effectively manage the end-to-end change lifecycle and identify process improvements where possible
Day to day management of change requests
Reporting of change to both internal and customer management teams
Identify and drive continuous improvements to the quality and efficiency of the change management process
Applies skills and develops documentation including operating procedures, process flow charts and manufacturing procedures
Documentation origination, editing and revision
Creation of change request and associated paperwork utilizing the Electronic Document Management System (EDMS)
Uses various computer software applications to complete assigned work activities
Understanding of compliance requirements and regulations Ability to generate report(s) utilizing the systems
Work with teams to determine status of projects/document changes and assist with driving project/document changes to completions
Be able to develop and speak to metrics and workload tracking
Be actively engaged in meetings
Participates in the development of solutions to Quality System problems and/or non-compliance
Assists in maintenance of department, site / business unit, and corporate procedures and policies
Demonstrates knowledge of operating procedures and expertise in a specific functional area
Accountable for the execution of specific tasks with moderate discretion and with oversight from a supervisor
Carries out tasks and activities
Applies specialized knowledge/skills to perform routine and non-routine work of a group or department
Other duties, as assigned
Requirements:
Quality Management Systems experience
Document Controls experience
Medical device industry experience
Highschool diploma and at least 1+ year experience in documentation related position
Basic understanding of regulations
Advanced language proficiency in reading, writing, understanding, and communicating in English
Attention to detail
Intermediate computer skills and software applications, including experience with Microsoft Office tools (Outlook, Word, Excel, PowerPoint)
Intermediate organizational and administrative skills
Experience in working in a cross-functional team environment as well as the ability to function independently
Ability to gather and organize information
Ability to grasp technical terms, processes, and methods
Ability to handle a variety of projects at the same time
Ability to prioritize and organize a busy and changing workload
Ability to work in a team environment and/or independently with little supervision
Works collaboratively with a variety of people at all levels within the organization to ensure effective communication and success of key initiatives
Resolve problems by clarifying issues
researching and exploring answers and alternative solutions
implements solutions
escalates unresolved problems
Ability to be flexible in work schedule, including a willingness to work overtime as needed