Pharma Manufacturing: Design & Technical Oversight Lead

AtkinsRéalis

Richmond (VA)

On-site

USD 170,000 - 210,000

Full time

14 days+
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Benefits offered by this job

Medical benefits
401(k) matching
Paid time off
Flexible work options

Job summary

AtkinsRéalis is seeking a Design Services & Technical Oversight Lead for the Pharmaceutical Manufacturing sector in the United States, overseeing owner-side technical activities across multiple projects. You will ensure GMP-aligned design decisions and lead independent design reviews with stakeholders from engineering, operations, and validation teams.

The role requires 20+ years in engineering leadership, EPC delivery experience, and a strong pharmaceutical/regulatory background.

Qualifications

  • Bachelor's degree in Engineering or related technical discipline; advanced degree preferred.
  • 20+ years of experience in engineering, design management, technical program leadership, EPC project delivery, or owner-side engineering oversight.
  • Pharmaceutical industry experience strongly preferred; experience in semiconductor, biotechnology, advanced manufacturing, chemical, data center, or other highly regulated industrial facilities will also be considered.

Responsibilities

  • Manage and lead owner-side technical oversight activities across multiple projects, facilities, and program workstreams.
  • Serve as the independent technical authority responsible for design quality, technical governance, and engineering assurance across EPC design packages.
  • Review engineering deliverables to ensure GMP compliance, operational expectations, site standards, and regulatory commitments.
  • Facilitate multidisciplinary design reviews involving engineering, operations, manufacturing, quality, validation, commissioning, maintenance, and construction stakeholders.
  • Evaluate design maturity, technical completeness, and engineering readiness in support of project gates, funding approvals, procurement activities, and construction execution.
  • Provide independent assessments of proposed technical solutions, identifying opportunities to improve operability, maintainability, reliability, safety, and schedule performance.

Skills

PE license
20+ years engineering experience
Pharmaceutical industry experience
EPC project delivery experience
Regulatory compliance GMP
Stakeholder management
Independent owner-side oversight

Education

Bachelor's degree in Engineering
Advanced degree preferred

Tools

Engineering governance systems
Document control platforms
Project management systems
Microsoft Office tools

Job description

AtkinsRéalis is seeking a Design Services & Technical Oversight Lead for the Pharmaceutical Manufacturing sector in the United States, overseeing owner-side technical activities across multiple projects. You will ensure GMP-aligned design decisions and lead independent design reviews with stakeholders from engineering, operations, and validation teams.

The role requires 20+ years in engineering leadership, EPC delivery experience, and a strong pharmaceutical/regulatory background.

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