Process Improvement Project Manager at Stantec
Town of Guilderland, New York, United States -
Full Time


Start Date

Immediate

Expiry Date

05 Jun, 26

Salary

160700.0

Posted On

07 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Project Management, Technical Engineering, Design Improvement, Corrective Action, Pharmaceutical Manufacturing, Data Collection Systems, CAPAs, cGMPs, Technical Writing, P&IDs, Financial Tracking, Schedule Management, Communication, Attention To Detail, Collaboration

Industry

Industrial Machinery Manufacturing

Description
We are seeking an experienced technical engineering Project Manager to lead design improvement and corrective action projects for various types of equipment used in pharmaceutical manufacturing. In this role, the team member will work at the client site and coordinate directly with multidisciplinary client teams to execute these projects and develop the associated technical documentation. The ideal candidate is a strong communicator with both technical and project management skills. Your Key Responsibilities * Lead planning, forecasting, and organization of multidisciplinary project teams for equipment design improvement projects in an FDA-regulated facility. Typical projects would include: * Developing a solution that integrates equipment with automated data collection systems and historian software * Adding alarms and permissive interlocks to automated equipment * Drive the implementation of Corrective and Preventative Action Plans (CAPAs) * Coordinate with automation, users, engineers, and technicians throughout the project life cycle * Execute projects in accordance with Client protocols and procedures, including the ability to use Client systems * Generate technical evaluations and test plans for changes associated with design improvement projects * Oversee financial tracking, project schedule, tasks, and project documentation * Manage projects for multiple pieces of equipment at a time Location Position location is for the Albany, NY office. 100% onsite presence at local client site is required.
Responsibilities
The Project Manager will lead planning, forecasting, and organization of multidisciplinary teams for equipment design improvement projects within an FDA-regulated facility, including developing solutions for automated data collection and driving CAPA implementation. Key duties involve coordinating with various technical staff throughout the project lifecycle, executing projects per client protocols, generating technical evaluations, and overseeing financial tracking and documentation.
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