Project Engineer-Design Lead

BioSpace

Richmond (VA)

On-site

USD 64,500 - 167,200

Full time

14 days+

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Benefits offered by this job

Comprehensive benefits program

401(k) with pension match

Employee wellness programs

Job summary

A global pharmaceutical leader is seeking a Project Engineer-Design Lead to oversee engineering design for capital projects. This role requires experience in pharmaceutical networks and offers compensation between $64,500 and $167,200 annually, along with comprehensive benefits. Candidates should have a BS in Engineering and 5 years of relevant experience. Key responsibilities include leading design standards, coordinating project teams, and facilitating decision making. The position is based in Richmond, VA with some travel expected.

Qualifications

Minimum of 5 years manufacturing and/or engineering experience supporting pharmaceutical or API networks.
Ability to work independently from long distances.

Responsibilities

Lead the identification of Engineering Design Standards.
Coordinate design for project phases with Project Manager.
Direct the development of design requirements.
Analyze inefficiencies and develop improvement strategies.
Support value engineering exercises.

Skills

Pharmaceutical process or project engineer experience

Strong project management skills

Effective facilitation of conflict resolution

Problem-solving ability

Understanding of capital project delivery

Education

BS in Engineering (Chemical or Mechanical preferred)

Job description

Position Overview

Join to apply for the Project Engineer-Design Lead role at BioSpace. This position supports the Global Facilities Delivery (GFD) Organization within Corporate Engineering and Continuous Improvement, delivering new and renovated capital assets worldwide. The Design Verification Lead (DVL) leads design oversight for capital projects focused on medical innovation, supply chain robustness, and expansion of existing medicines.

Responsibilities

Lead the identification of applicable Engineering Design Standards, Engineering Functional Standards, Engineering Specifications and Regulatory requirements and guidance (both internal and external).
Be responsible for the overall design delivery for capital project(s).
Coordinate all design for the Project Manager during all design phases and ensure delivery of the conceptual design review and basic design review.
Direct the development of design requirements and assist in developing and maintaining the design schedule.
Participate in the selection of A/E firms and coordinate with them to develop earned value progress systems to measure progress by discipline.
Expedite design decisions and coordinate information flow between the design team and system owners.
Ensure designs meet approved intent through interactions between the design firm, design specialists, Engineering Tech Center disciplines, and end user/customer.
Resolve design-related problems and enforce design governance.
Analyze inefficiencies and develop strategies for improvement to meet or improve design hours plan.
Assist in developing SOPs, project delivery work instructions, and best practices related to design/verification.
Review and approve key design project personnel with the Project Manager.
Work with Engineering Tech Center resources to address and resolve design issues.
Support replication in design when applicable.
Assist the Project Manager with value engineering exercises.
Review design-related invoices and participate in KPI reviews/assessments.
Select verification professional services and develop the Project Verification Plan, Traceability Matrix, and risk assessments.
Coordinate verification for the Project Manager during verification phase and manage discrepancy tracking.

Basic Requirements

BS in Engineering (Chemical or Mechanical preferred).
Minimum of 5 years manufacturing and/or engineering experience supporting pharmaceutical or API networks.

Additional Preferences

Pharmaceutical process or project engineer experience.
Strong project management skills.
Effective facilitation of conflict resolution and influencing across all levels of the project.
Understanding of capital project delivery process, A/E design activities, and Lilly technical resources.
Alignment with Lilly values.
Ability to frame complex decisions, facilitate decision making, and implement plans.
Experience in issue resolution, scope change anticipation, and safe, quality, speed, and value delivery.
Willingness to relocate and/or travel to locations outside home state/country; ability to work independently from long distances.

Additional Information

Travel can be domestic and international, averaging about 25%, depending on project phase.
Potential co‑location at the A/E firm or job site to support C&Q activities for periods of time based on project needs.

Compensation & Benefits

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $64,500 - $167,200 per year.

Full‑time employees are eligible for a company bonus (based on company and individual performance). In addition, Lilly offers a comprehensive benefits program: 401(k) with pension match, vacation and leave packages, medical, dental, vision and prescription drug coverage, flexible spending accounts, life insurance, employee wellness programs, and more. Lilly reserves the right to amend its compensation and benefit programs in its sole discretion.

EEO & Accessibility

Lilly is dedicated to helping individuals with disabilities actively engage in the workforce, ensuring equal opportunities. If you require accommodation to apply, please complete the accommodation request form at https://careers.lilly.com/us/en/workplace-accommodation.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Seniority Level