GMP-Driven Engineering & Project Lead (Onsite)

Akraya; Meriden (CT); On-site; USD 83,000 - 96,000; Full time

Job summary

Akraya, Inc. seeks a Project Manager to join the capital engineering team in Meriden, CT onsite. This 12-month contract role focuses on managing facility projects from concept through completion, ensuring quality, safety and optimal performance.

You will oversee design firms, contractors, and vendors, track progress against scope and budget, and drive continuous improvement in facility operations to boost utilization and cost-effectiveness.

Qualifications

• Experience managing projects within defined constraints.
• Excellent technical writing and documentation skills.
• Experience drafting RFPs and RFQs and protocols in GMP/FDA/ISO contexts.
• Familiarity with medical device or biopharma manufacturing standards.
• Experience with manufacturing environment standards.

Responsibilities

• Oversee projects from feasibility through construction.
• Manage design firms, contractors, and vendors.
• Track progress against scope, budget, and schedule.
• Ensure adherence to quality and safety standards.
• Drive continuous improvement in facility operations.

Skills

Project management

Technical writing

Vendor management

GMP FDA ISO

Manufacturing standards

RFPs RFQs

Documentation

Job description

Akraya, Inc. seeks a Project Manager to join the capital engineering team in Meriden, CT onsite. This 12-month contract role focuses on managing facility projects from concept through completion, ensuring quality, safety and optimal performance.

You will oversee design firms, contractors, and vendors, track progress against scope and budget, and drive continuous improvement in facility operations to boost utilization and cost-effectiveness.