Electrical Project Lead (Pharma) – On-Site Fall River

Cipla

Fall River (MA)

On-site

USD 76,000 - 103,000

Full time

10 days ago

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Job summary

Cipla in Fall River, MA, seeks a Project Lead - Electrical (Supervisor) to direct electrical engineering projects in a cGMP pharmaceutical environment. You will oversee design reviews, equipment qualification, vendor coordination, and CapEx planning to ensure on-time, within-budget execution.

The role requires a Bachelor’s degree in Engineering, 5+ years in pharma/biotech engineering and validation, strong knowledge of SAP, MS Project/Primavera, and excellent communication. PMP is a plus; U.S.

Qualifications

  • Bachelor’s degree in Engineering (Mechanical, Electrical, or related field).
  • Minimum 5 years of pharma/biotech engineering and validation project management.
  • Strong knowledge of sterile manufacturing processes.
  • Experience with validation lifecycle documentation and execution.
  • Familiarity with project management tools (MS Project, Primavera).
  • Experience with SAP for engineering and financial operations.
  • PMP certification is a plus.
  • Excellent communication, leadership, and problem-solving skills.

Responsibilities

  • Design, review and approve protocols for electrical equipment and processes.
  • Ensure cGMP compliance and regulatory requirements in all designs.
  • Oversee installation, commissioning and qualification of electrical systems.
  • Prepare Capital Expenditure (CapEx) requests with ROI analysis.
  • Coordinate with QA, Validation, Regulatory Affairs and vendors.
  • Manage project budgets and track CAPEX performance.

Skills

Project leadership
Communication
Problem solving
Team coordination
Regulatory awareness

Education

Bachelor’s degree in Engineering
Master’s degree preferred
PMP certification

Tools

SAP
MS Project
Primavera

Job description

Cipla in Fall River, MA, seeks a Project Lead - Electrical (Supervisor) to direct electrical engineering projects in a cGMP pharmaceutical environment. You will oversee design reviews, equipment qualification, vendor coordination, and CapEx planning to ensure on-time, within-budget execution.

The role requires a Bachelor’s degree in Engineering, 5+ years in pharma/biotech engineering and validation, strong knowledge of SAP, MS Project/Primavera, and excellent communication. PMP is a plus; U.S.

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