Genovice

7 jobs near Columbus, OH

Capital Project Engineer - Pharmaceutical Manufacturing Location: Wilmington, Delaware We are seeking two experienced Capital Project Engineers to support the startup of a new pharmaceutical ...

CSV Validation Engineer

Atlanta, GA · Remote

$90K - $125K/hr

This is a remote position. SR CSV Validation Engineer Location: Remote Role type: Contract The Opportunity A growing technology company serving pharmaceutical and other regulated manufacturing ...

GMP Technical Writer

Indianapolis, IN · Hybrid

$70K - $100K/hr

This is a remote position. GMP Technical Writer - Engineering Location: Indianapolis, IN / Remote Hybrid Type: Contract Travel/On-Site: Initial 1 week on-site in Indianapolis, followed by ...

QA Documentation Specialist Location: San Diego, CA Type: Full Time Industry: Pharmaceutical Manufacturing Position Overview Our client is seeking a QA Documentation Specialist to support the ...

This is a remote position. CSV Quality Engineer Lead- Part-Time Location: Remote Commitment: Approximately 20 hours per week Role type: Part-time The Opportunity A growing technology company serving ...

Capital Project Engineer

Genovice

Wilmington, DE • On-site

$50 - $60/hr

Full-time

Posted 6 days ago


Job description

Capital Project Engineer – Pharmaceutical Manufacturing
Location: Wilmington, Delaware

We are seeking two experienced Capital Project Engineers to support the startup of a new pharmaceutical manufacturing facility in Wilmington, Delaware. One engineer will focus primarily on a lyophilizer, while the other will focus on a pharmaceutical filling line.

Key responsibilities:

  • Lead capital engineering activities for assigned manufacturing equipment from installation through startup and operational readiness.

  • Support the installation, commissioning, qualification, and startup of a lyophilizer or filling line.

  • Coordinate with equipment vendors, contractors, Engineering, Manufacturing, Automation, Quality, and Validation teams.

  • Review equipment specifications, drawings, design documents, and vendor documentation.

  • Support FAT, SAT, commissioning, troubleshooting, and turnover activities.

  • Track project schedules, equipment deliverables, technical issues, and action items.

  • Ensure equipment and project activities comply with GMP requirements, engineering standards, and applicable safety regulations.

  • Support the development and execution of equipment turnover and qualification documentation.

Qualifications:

  • Bachelor’s degree in Mechanical, Chemical, Electrical, or a related engineering discipline.

  • Capital project engineering experience within a pharmaceutical, biotechnology, or other regulated manufacturing environment.

  • Hands-on experience bringing pharmaceutical manufacturing equipment online.

  • Direct experience with either lyophilizers or sterile/aseptic filling equipment is strongly preferred.

  • Working knowledge of GMP requirements and commissioning and qualification practices.

  • Strong vendor-management, troubleshooting, and cross-functional communication skills.

  • Ability to work onsite at the Wilmington, Delaware facility as required.