About the Role
A validation and quality assurance provider is looking to hire a Project Engineering Manager for their Albany, NY project site. This is a 6-to-24-month assignment with possible extension. This unique group works to develop and blueprint a universally implemented validation process that reliably achieves quality, affordable and available healthcare products.
Hourly rate is $50.00 to $75.00.
Responsibilities:
Assigned to specific capital equipment project(s)
Work direction provided by designated Engineering resources
Integrated into existing engineering workforce
Assigned multiple projects and/or project tasks based on business needs
Reports directly to Engineering Project Manager
Execute engineering design, analysis, and documentation tasks
Prepare technical specifications, drawings, and calculations
Conduct engineering reviews and assessments
Prepare and execute test protocols (e.g., FAT, SAT, change control test plan)
Oversee equipment installation, assembly, and/or construction activities
Support project planning, scheduling, and execution
Participate in design reviews, safety assessments, and technical meetings
Coordinate with cross-functional teams (Operations, QA, Facilities, etc.)
Project Management Support
Assist in project scope development and requirements definition
Support budget tracking and cost management activities
Maintain and organize project documentation and records
Prepare progress reports and status updates as requested
Facilitate vendor/contractor coordination as directed
Schedule meetings and generate meeting minutes
Regulatory and Compliance Activities
Ensure designs comply with FDA, cGMP, and other applicable regulations
Support validation activities (IQ/OQ/PQ)
Execute and maintain documentation per client standards
DELIVERABLES
Technical drawings and specifications
Engineering calculations and analyses
Project schedules and progress reports
Risk assessments and mitigation plans
Design review documentation
Test protocols
Validation and commissioning documentation
Project status reports
Requirements:
Bachelorâs degree in engineering (Chemical, Mechanical, Electrical, or related field)
Minimum 5 years of Engineering experience in pharmaceutical/biotechnology industry
Knowledge of cGMP regulations and FDA requirements
Proficiency in relevant engineering software (MS Project, MS Excel, AutoCAD, etc.)
Prior experience with bioprocessing equipment design, installation, and verification testing
Project management experience
JSG has been named to three prestigious lists from Staffing Industry Analysts (SIA)âs: Largest Staffing Firms in the U.S., Largest Engineering Staffing Firms in the U.S., and Largest Staffing Firms in Canada.
Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law.
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