Entry Level CQV Engineering Professional
The Entry Level CQV Engineer at Confidential Client supports life sciences clients by ensuring commissioning, qualification, and validation activities meet industry standards and client requirements. This role involves developing and executing CQV protocols, reviewing technical drawings, and preparing documentation, while working collaboratively on GMP manufacturing projects. The position offers mentorship and growth opportunities within a dynamic, client-focused environment.
About Careertakes
👉 Important disclosure: Careertakes is a third-party recruiting platform supporting this hiring process. If selected, you will be employed directly by our client, Engineering (Life Sciences).
Applicants for this role may also receive access to additional matched opportunities through the Careertakes platform.
Overview
Confidential Client is hiring an Entry Level Commissioning, Qualification & Validation (CQV) Engineering Professional to join a Life Sciences engineering team supporting GMP facilities. This is a full-time, entry-level engineering role based in Uptown, IN. The role includes mentorship, hands-on CQV work on client sites, and opportunities to develop technical documentation and field verification skills.
What You’ll Do
- Support commissioning, qualification, and validation activities for GMP manufacturing facilities.
- Develop and execute CQV protocols and reports using Good Documentation Practices (GDP).
- Inspect and verify facility and equipment drawings (P&IDs, AF&IDs) in the field.
- Prepare Construction Turnover Packages, SOPs, and process workflows.
- Investigate and help resolve protocol exceptions and discrepancies.
- Collaborate with cross-functional project teams and follow recognized codes, standards, and customer requirements.
- Travel to client sites as required and work on multiple projects under mentorship.
Minimum Qualifications
- Bachelor’s degree in Chemical Engineering or a closely related engineering discipline.
- 3.0 GPA or higher (as indicated in source posting).
- Legal authorization to work in the U.S. without sponsorship now or in the future.
- Strong written and verbal communication skills.
- Proficient with Microsoft Office (Word, Excel, PowerPoint; Project is a plus).
- Highly organized, able to multitask, and comfortable working in field and client-site environments.
Preferred / Nice-to-Have
- Local to Uptown, IN (or willing to relocate).
- Coursework or internship experience related to validation, process engineering, or GxP environments.
- Familiarity with GMP concepts and life-sciences project workflows.
- Willingness to travel and adapt to various client locations.
Compensation & Location
- Estimated annual pay (from source): $59,849 per year (estimated).
- Location: Uptown, IN — on-site / client-site work expected; travel required as projects demand.
- Employment type: Full-time.
Additional Notes & Legal Compliance
- Confidential Client and Careertakes are committed to hiring in compliance with applicable U.S. federal, state, and local employment laws. Reasonable accommodations are available for applicants with disabilities during the application and hiring process; please let us know if you need an accommodation.
- Ability to work in the U.S. without sponsorship is required for this role (as stated in the source).
- This posting does not guarantee any particular start date; the source indicated a target December/January start window.
Equal Opportunity & Hiring Transparency
Careertakes and our client are Equal Opportunity Employers committed to building a diverse and inclusive workforce. We prohibit discrimination or harassment of any kind. To support a fair and efficient hiring process, AI tools may be used to assist with application review or resume screening. These tools do not replace human decision-making. Final hiring decisions are made by people.
If you have questions about how your data is used, please contact us directly.
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