Why This Role Stands Out
Leverage your expertise in GMP environments to drive critical equipment commissioning and qualification projects at a reputable pharmaceutical site, gaining valuable experience in a regulated setting. This role is ideal for a detail-oriented engineer with a strong understanding of validation protocols and a desire to contribute to compliant operations. Apply now to enhance your skills and advance your career in pharmaceutical engineering.
Quick Overview
Job Description
We are seeking an Equipment Commissioning & Qualification Engineer to support the implementation, qualification, validation, and continued compliant operation of equipment, instruments, facilities, and utilities at a GMP-regulated pharmaceutical site.
The engineer will develop and execute commissioning and qualification protocols, prepare validation and qualification documentation, coordinate external vendors, and support equipment implementation from site preparation and installation through qualification and turnover. The role will also support change management, equipment lifecycle activities, technical troubleshooting, and deviation investigations as needed.
Position details:
• Hourly rate: $55.7–$60.7;
• Contract length: 6 months, with possible extension based on performance;
• Start date: August 17, 2026;
• Location: Summit, New Jersey;
• Work arrangement: 100% onsite;
• Schedule: Monday–Friday, normal business hours;
• Maximum hours: 40 hours per week;
• W-2 contract position;
• No C2C options;
• No visa sponsorship.
Required:
• Minimum of 5 years of experience performing or supporting activities in a GMP-regulated environment;
• Minimum of 3 years of experience in equipment, facilities, or utilities qualification;
• Experience developing and executing commissioning, qualification, or validation protocols and associated reports;
• Experience preparing qualification deliverables such as Validation Plans, Requirements Specifications, Design Specifications, Traceability Matrices, and Summary Reports;
• Knowledge of cGMP, GxP, GAMP, SDLC, 21 CFR Part 11, computerized systems validation requirements, and good documentation practices;
• Knowledge of pharmaceutical manufacturing and laboratory systems;
• Understanding of investigations, deviations, CAPA, and change management in a regulated pharmaceutical environment;
• Ability to supervise vendors and manage equipment implementation or qualification activities;
• Ability to manage multiple projects, priorities, and assignments in a fast-paced environment;
• Strong written, verbal, organizational, analytical, and interpersonal skills;
• Proficiency in Microsoft Word, Excel, PowerPoint, Outlook, and database systems;
• Authorization to work in the United States without visa sponsorship.
Preferred:
• Bachelor’s degree in Engineering or a science-related discipline; sufficient relevant experience may substitute for the degree;
• Experience with ValGenesis.
• Health insurance with dental and vision insurance options.
• Holiday pay.
• 401(k) program.
• Employee referral bonus program.
• Possible contract extension based on performance.
• The client retains the right to hire the contractor directly.
Similar jobs
- EG
HIL ENGINEER
NewEmpresent Global, LLC
Palo Alto, CA🇺🇸Hybrid17 hours agoSimulinkEngineering - IN
Staff Mechanical Design Engineer
Intuitive
Sunnyvale, CA🇺🇸On-site5 weeks agoRoboticsCADMechanical Design+1Engineering - HA
Engineering Leadership Development Program - Mechanical Engineer (Various Locations)
Harris Corporation
Melbourne, FL🇺🇸$68k/yrHybrid1 week agoCADFEAMechanical Design+1Engineering - AI
Senior Robotics Engineer, Maritime
NewANDURIL INDUSTRIES
Quincy, MA🇺🇸$220k - $292k/yrHybrid17 hours agoRoboticsEngineering - QE
Senior Drilling Engineer
NewQuaise Energy, Inc
Denver🇺🇸17 hours agoComplianceContinuous ImprovementLESS+3Engineering - MI
Mechanical Designer - Airborne
NewMatter Intelligence
El Segundo🇺🇸15 hours agoRoboticsAssembly