Manufacturing Project Manager

Manufacturing Project Manager

08 Nov 2024
California, Pleasantonca 00000 Pleasantonca USA

Manufacturing Project Manager

Vacancy expired!

Client Abbott
Role Manufacturing PM
Location Pleasanton, CA
Buy rate - $58/hr

MCS Technical Project Manager

Job Description
>10 years Medical device industry experience
Primary Responsibilities:
Manages complex manufacturing implementation of medical device projects within the Business Unit
Guides development and documentation of packaging, labeling, product manuals, and manufacturing procedures and resolves team obstacles.
Assures the development of multi-level project planning to achieve short and long-term business objectives
Keeps senior management team informed of development/implementation progress and issues.
Develops functional departmental budgets and coordinates cross-functional project budgets
Develops and communicates key performance indicators (cost/schedule/technical/quality) for projects.
Provides design/development teams with appropriate resources to perform assigned tasks.
Interfaces with appropriate internal resources (regulatory, quality, manufacturing engineering, etc.) and external suppliers to ensure development programs meet quality and customer requirements.
Reviews and provides functional approval for project and quality system documentation.
Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
Education & Experience You'll Bring:
Bachelor's Degree in a technical field (i.e. Sciences, Engineering) or related discipline
5+ years of medical device development experience and managing complex, multi discipline (manufacturing, labeling, mechanical) devices
Managed cross discipline (Quality, Regulatory, Operations, Marketing, etc) development teams and/or programs
Working knowledge and experience with 21 CFR 820.30 and European Medical Device Directive (application to medical devices); European MDR experience also helpful.
Proficient with MS Project, Excel, and PowerPoint as well as electronic document control systems
Budget planning and management experience
Excellent verbal and written communication skills, with ability to communicate to all levels of the organization
Experience collaborating with cross-functional teams in a geographically diverse, matrixed organization
Ability to travel 10% of the time
Preferred Qualifications:
Advanced level degree in technical and/or science field or related discipline
PMP certification
Medical Device Labeling experienc

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