On-Site Construction Manager – Pharma GMP Projects

Unicon Pharma Inc

Portsmouth (NH)

On-site

USD 90,000 - 130,000

Full time

40 hours ago
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Job summary

Unicon Pharma Inc is seeking an experienced Construction Manager to lead on-site pharmaceutical engineering projects in Portsmouth, NH. You will monitor contractors, ensure PPE and safety compliance, review drawings, and coordinate with the CADD group to maintain up-to-date TOP package documentation.

The role requires 5–7 years in pharmaceutical engineering and industrial construction management, strong communication, and deep knowledge of change controls and GMP practices.

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.

Responsibilities

  • Daily on-site construction management for multiple projects, monitoring PPE and safety compliance.
  • Escalating concerns to manager or stakeholders as required.
  • Coordinate scheduling of construction-related activities and communicate outages to affected parties.
  • Redline drawings for as-building and coordinate with CADD group to update drawings and TOP package docs.
  • Ensure construction work proceeds on schedule and meets drawings and project specs.
  • Draft change controls with Quality Group and gain stakeholder alignment.
  • Gather pricing and assist with scoping upcoming projects.
  • Work with vendors to specify and gather budgetary pricing for equipment.
  • Setup spare parts and main plans in SAP.

Skills

Excellent written and verbal comms
Change controls
GMP manufacturing practices
Construction management

Tools

SAP

Job description

Unicon Pharma Inc is seeking an experienced Construction Manager to lead on-site pharmaceutical engineering projects in Portsmouth, NH. You will monitor contractors, ensure PPE and safety compliance, review drawings, and coordinate with the CADD group to maintain up-to-date TOP package documentation.

The role requires 5–7 years in pharmaceutical engineering and industrial construction management, strong communication, and deep knowledge of change controls and GMP practices.

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