Job Description
Position: Sr Validation Engineer
Location: Waukegan, IL 60087 onsite 5 days a week
Duration: 12+ months
Pay Rate $60.00 -$75.00 per hour W2 + Benefits
I am looking for a CQV Project Lead to independently manage equipment qualification projects within an API Pilot Plant and clinical drug-substance manufacturing environment. This role primarily supports process and equipment CQV—not facilities validation.
The ideal candidate has 10+ years of pharmaceutical commissioning, qualification, or validation experience and can independently develop, execute, and close complete qualification packages.
Responsibilities
- Independently own CQV projects and qualification packages from planning through final closeout.
- Develop and execute commissioning, IQ, OQ, and PQ protocols.
- Qualify pharmaceutical process and portable equipment.
- Support reactors, mix tanks, process piping, instrumentation, and potent-compound isolators.
- Review P&IDs, equipment drawings, specifications, and turnover documentation.
- Conduct equipment walkdowns and installation verification.
- Document discrepancies and manage deviations, punch lists, and protocol exceptions through closure.
- Support nitrogen and process-piping utility qualification.
- Coordinate with Engineering, Manufacturing, Quality, Automation, vendors, and other project stakeholders.
- Maintain accurate, traceable, and inspection-ready GMP documentation.
- Author and execute qualification documentation using Kneat when applicable.
QUALIFICATIONS
- 10+ years of pharmaceutical CQV or validation experience.
- Hands-on experience developing and executing IQ, OQ, and PQ protocols.
- Ability to independently own qualification packages and manage CQV projects.
- Strong process-equipment qualification experience.
- Experience reviewing P&IDs and technical equipment documentation.
- Experience managing deviations, discrepancies, and punch-list items.
- Strong GMP documentation and change-control experience.
- API, small-molecule, drug-substance, pilot-plant, or specialty chemical manufacturing experience.
- Experience qualifying reactors, mix tanks, process piping, instrumentation, portable equipment, or potent-compound isolators.
- ADC or biotechnology manufacturing experience.
- Experience with single-use systems, single-use mixers, UF/DF systems, Cytiva equipment, or antibody-processing equipment.
- Kneat or Kneat Gx experience.
- DeltaV or PLC validation experience.
- Experience performing I/O checks and verifying controls, HMI screens, alarms, interlocks, and operating sequences.
- Nitrogen or process-piping utility qualification experience.
About us…Sterling Engineering, in business for 57 years …we offer FULL BENEFITS! As a Sterling Engineering W2 employee on contract, you receive a Full Employee Benefits Package that includes Paid Time Off, Paid Holidays, 3 Medical plans to choose from, Dental & Vision plans, 401(k) with a match, and an Employee Stock Ownership (ESOP) plan.
Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.
Numbers & Facts
| Location | Waukegan, IL |
| Industry | Staffing/Employment Agencies |
| Salary | $60–$75 Per Hour |
| Company Size | 500 to 999 employees |
| Year Founded | 1969 |
| Website | http://www.sterling-engineering.com |
About Company
Sterling Engineering has been a trusted partner for engineering, project management, and staffing solutions for over five decades. We provide exceptional engineering/technical recruitment and engineering project services to clients nationwide:
- Engineering & Technical Recruitment - With our focus on engineering, technical, and IT, Sterling has the in-depth knowledge, industry expertise, and robust employee pipeline it takes to rapidly find talent for even the most difficult to fill positions. Sterling’s extensive recruitment methodology allows us to engage the most talented employees in the marketplace. We offer exciting work and career-building opportunities for our candidates, along with expert support at every step of the process.
- Engineering Project Services – Our experienced, multi-disciplined team of project managers, engineers, and designers, led by licensed Professional Engineers (PE), provide project management, engineering, design, and Commissioning, Qualification, and Validation (CQV) to manufacturing, OEM, and R&D customers. We work on complex, highly technical projects across a number of industry sectors, and our ability to scale and seamlessly integrate at multiple levels of your organization is what differentiates us.
Sterling offers a unique combination of engineering solutions and Best of Staffing level service to help our clients and talent achieve their goals.
Skills
- Active Pharmaceutical Ingredient (API)unmatched
- Antibodiesunmatched
- Automationunmatched
- Biotech and Pharmaceuticalunmatched
- Commissioningunmatched
- DeltaVunmatched
- Documentationunmatched
- Drug Manufacturingunmatched
- Equipment Specificationunmatched
- GMP (Good Manufacturing Practices)unmatched
- Human Machine Interface (HMI)unmatched
- Input/Outputunmatched
- Instrumentationunmatched
- Manufacturingunmatched
- Pilot Plantunmatched
- Pipingunmatched
- Process Validationunmatched
- Programmable Logic Controller (PLC)unmatched
- Project/Program Managementunmatched
- Small Molecule Drugsunmatched
- Technical Writingunmatched
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