On-Site Pharma Construction Manager (Mid-Level)

Aequor Information Technologies Pvt. Ltd.; Portsmouth (NH); On-site; USD 90,000 - 120,000; Full time

Job summary

Aequor Information Technologies Pvt. Ltd. in Portsmouth, NH seeks a mid-level Manager, Construction Engineering to lead on-site construction activities for multiple pharmaceutical projects. You will monitor contractors, enforce PPE and safety, and coordinate outages with stakeholders.

The role requires reading blueprints and P&IDs, redlining design docs, and coordinating with CADD and QA for change controls to ensure GMP-compliant construction. Prior pharma facility experience is preferred.

Qualifications

• 5-7 years in Pharmaceutical Engineering Projects and Industrial Construction Management.
• Excellent written and verbal communication skills.
• Extensive knowledge of Change Controls and GMP manufacturing practices.
• Familiar with utilities (Clean and Black) and internal Safety Permitting processes.
• Ability to read blueprints/site design documents and redline design docs with as-built results.

Responsibilities

• Daily on-site Construction Management for multiple projects – monitor contractors for PPE and safety compliance, escalating concerns as required.
• Coordinate with stakeholders to schedule construction activities and communicate outages.
• Redline drawings for as-building and work with CADD to update drawings and assemble TOP package docs.
• Ensure work proceeds on schedule and meets drawings and project specifications at high quality.
• Work with Quality to draft change controls and gain stakeholder alignment.
• Gather pricing and assist with scoping upcoming projects.

Skills

Communication skills

GMP knowledge

Change controls

On-site mgmt

P&ID walkdown

Tools

SAP

Job description

Aequor Information Technologies Pvt. Ltd. in Portsmouth, NH seeks a mid-level Manager, Construction Engineering to lead on-site construction activities for multiple pharmaceutical projects. You will monitor contractors, enforce PPE and safety, and coordinate outages with stakeholders.

The role requires reading blueprints and P&IDs, redlining design docs, and coordinating with CADD and QA for change controls to ensure GMP-compliant construction. Prior pharma facility experience is preferred.