Project Engineer – Life Sciences

Pyramid Consulting, Inc; St. Louis (MO); On-site; USD 110,000 - 165,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Paid sick leave

Job summary

Pyramid Consulting, Inc. is seeking a Project Engineer – Life Sciences for a 6 to 12 months contract onsite in St. Louis, MO.

The role requires coordinating contractors and design firms, ensuring GMP, codes and safety, and supporting scope, schedule and budget development. The candidate will act as liaison among project teams and owner resources, aiding transfer and consolidation of manufacturing operations.

Qualifications

• Bachelor's Degree in Engineering and at least 5 years in pharma/Life Sciences GMP manufacturing.
• Direct experience with EPC/design firms and construction contractors on facility modifications and manufacturing consolidation.
• Experience with consolidation and transfer of tableting, packaging, and powder down-filling operations.

Responsibilities

• Coordinate contractors, design firms, technical teams, documentation, and project execution while ensuring GMP compliance and safety.
• Manage documentation to ensure RFIs, submittals, and design deliverables meet client requirements.
• Act as liaison between Technical Project Lead, contractors, design team, and owner resources.
• Ensure compliance with building codes, end-user requirements, and site-specific requirements during development and execution.
• Assist with project scope, schedule, budget, risk and change management, and other deliverables.
• Provide technical support and assist in issue resolution during development and execution.
• Support project consolidation and execution activities for manufacturing operations consolidation.

Skills

Contractor coordination

Documentation management

GMP knowledge

Project coordination

Education

Bachelor's Degree in Engineering

Job description

Immediate need for a talented Project Engineer – Life Sciences. This is a 06 to 12 months contract opportunity with long-term potential and is located in St. Louis, MO (Onsite). Please review the job description below and contact me ASAP if you are interested.

Job Diva ID: 26-23830

Pay Range: $80 to $120/hourly.

Employee benefits include, but are not limited to,

• health insurance (medical, dental, vision)
• 401(k) plan
• paid sick leave (depending on work location)

Key Responsibilities;

• The client is seeking a Project Engineer to support a Design/Build pharmaceutical manufacturing consolidation project on the owner’s side. The ideal candidate will have strong experience coordinating contractors, design firms, technical teams, documentation, and project execution while ensuring compliance with GMP, building codes, safety, engineering standards, and end-user requirements.
• Manage contractor and design firm generated documentation to ensure RFIs, submittals, design firm deliverables, etc. comply with our client requirements.
• Act as liaison between Technical Project Lead, contractors, design team, and owner technical resources throughout project.
• Ensure all work complies with relevant building codes, end user requirements, engineering practices, safety guidelines and regulations, and site specific requirements throughout development and execution of project.
• Assist Technical Project Lead with project scope, schedule, and budget development, risk and change management, and other project deliverables as needed.
• Provide technical support and assist in resolution of issues that arise during project development and execution.
• Here’s the high level description of the project the candidate would be supporting:
• The project will consolidate tableting manufacturing and packaging operations from three St. Louis facilities into a single operational space, while also consolidating powder down-filling operations from two facilities into separate animal and non‑animal production areas within one facility.
• All manufacturing and packaging processes will be transferred as part of this initiative.

Key Requirements and Technology Experience:

• Must a Bachelor’s Degree in Engineering and min 5 years of experience within pharmaceutical, life sciences, GMP manufacturing, chemical, or regulated manufacturing facility projects or industries.
• Candidate should have direct working experience with EPC/design firms and construction contractors on facility modifications, equipment/process transfers, or manufacturing consolidation projects.
• Candidate must have understanding on consolidation and transfer of tableting, packaging, and powder down-filling manufacturing operations.

Our client is a leading Life Sciences Industry, and we are currently interviewing to fill this and other similar contract positions.

Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.