Project Manager 3
Share
Job Location:
Sunnyvale, CA - USA
Monthly Salary:
Not Disclosed
Posted on:
7 hours ago
Vacancies:
1 Vacancy
Job Summary
Job Title: Project Manager 3
Location: Sunnyvale CA 94043
Duration: 12 Months
Pay Rate: $70.00 - $78.00/- on W2
Kindly help me out with your most updated resume
Roles and Responsibilities:
The Project Manager creates and manages project schedules to support the development of internal Quality Management System (QMS) documentation for a medical device company.
Work with technical writers Subject Matter Experts (SMEs) and core teams to outline the scope of the documentation and Identify all affected documentation to be created or updated.
Create schedules for documentation deliverables.
Work cross-functionally with SMEs and core teams to create strategy and timeline to support business needs.
Identify communicate and help resolve risks resource overloads and content creation or revision constraints.
Represent technical publications function on core teams.
Coordinate with technical publications management on resource needs and project timelines.
Establish deadlines and support needs with external translation vendors.
Understand Regulatory Standards Document Control and Quality Assurance requirements for process documentation.
Ensure Good Documentation Practices (GDP) are followed per relevant procedures.
Participate in and initiate department process improvement projects.
Flexible to support various other duties and assignments as requested to assist the overall function of the department.
Skills Experience Education & Training:
3-8 years of project management preferred
Bachelors degree in related field or equivalent work experience preferred
PMP certification preferred
Strong communication and presentation skills required
Strong interpersonal skills and ability to interact with core team leaders and other functions required
Strong organizational skills and ability to manage deliverables for multiple projects under tight deadlines set priorities and manage time effectively
Creation of project schedules required
Experience in a regulated environment required
Experience with medical devices in an FDA and internationally regulated environment preferred
Extensive knowledge of project management processes organizational change management concepts and business process improvement and documentation methods required
Ability to multi-task and work both in a team and independently required
Experience with change management software (Agile or equivalent) highly preferred
Highly organized with good analytical skills preferred
Understanding of localization process preferred
Work with technical writers Subject Matter Experts (SMEs) and core teams to outline the scope of the documentation and Identify all affected documentation to be created or updated.
Create schedules for documentation deliverables.
Work cross-functionally with SMEs and core teams to create strategy and timeline to support business needs.
Identify communicate and help resolve risks resource overloads and content creation or revision constraints.
Represent technical publications function on core teams.
Coordinate with technical publications management on resource needs and project timelines.
Establish deadlines and support needs with external translation vendors.
Understand Regulatory Standards Document Control and Quality Assurance requirements for process documentation.
Ensure Good Documentation Practices (GDP) are followed per relevant procedures.
Participate in and initiate department process improvement projects.
Flexible to support various other duties and assignments as requested to assist the overall function of the department.
Skills Experience Education & Training:
3-8 years of project management preferred
Bachelors degree in related field or equivalent work experience preferred
PMP certification preferred
Strong communication and presentation skills required
Strong interpersonal skills and ability to interact with core team leaders and other functions required
Strong organizational skills and ability to manage deliverables for multiple projects under tight deadlines set priorities and manage time effectively
Creation of project schedules required
Experience in a regulated environment required
Experience with medical devices in an FDA and internationally regulated environment preferred
Extensive knowledge of project management processes organizational change management concepts and business process improvement and documentation methods required
Ability to multi-task and work both in a team and independently required
Experience with change management software (Agile or equivalent) highly preferred
Highly organized with good analytical skills preferred
Understanding of localization process preferred
Key Skills
- Project Management Methodology
- Project / Program Management
- Construction Estimating
- Construction Experience
- PMBOK
- Visio
- Construction Management
- Project Management
- Project Management Software
- Microsoft Project
- Project Management Lifecycle
- Contracts
