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.

Applicants for this role may also receive access to additional matched opportunities through the Careertakes platform.

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What You’ll Do

This entry-level Commissioning, Qualification & Validation (CQV) role supports life sciences projects ensuring systems, equipment, and facilities are installed, commissioned, and validated to meet functional specifications, codes, and GMP expectations. You will join a Confidential Client team working on regulated manufacturing environments and will receive hands-on mentorship to grow technical skills and careers in CQV.

• Develop, review, and execute CQV protocols (IQ/OQ/PQ) using Good Documentation Practices (GDPs).
• Investigate and document protocol exceptions, deviations, and corrective actions.
• Prepare technical and CQV summary reports for client review.
• Verify field and facility drawings (P&IDs, AF&IDs) and confirm installation per design.
• Support development of SOPs, process workflows, and Construction Turnover Packages.
• Participate in installation and operational testing activities, coordinating with construction and commissioning teams.
• Communicate technical findings clearly with clients and project teams; support project schedules and travel to client sites as needed.

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Qualifications

Minimum requirements:

• Bachelor’s degree in Chemical Engineering or a closely related engineering discipline.
• 3.0 GPA or higher (or equivalent academic achievement).
• Authorization to work in the U.S. without the need for sponsorship now or in the future.
• Strong attention to detail, organization, and the ability to manage multiple tasks.

Preferred:

• Local to Conshohocken, PA or willing to commute/relocate and travel to client sites.
• Familiarity reading P&IDs, AF&IDs, and engineering drawings.
• Proficient with Microsoft Office (Word, Excel, PowerPoint, Project).
• Excellent written and verbal communication skills.

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Compensation & Location

• Location: Conshohocken, PA (on-site and client-site work as required).
• Employment type: Full-time.
• Estimated compensation: $71,315 per year (estimated). Note: actual offer and total compensation will be provided by the Confidential Client.

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Preferred Skills & Tools

• Commissioning, Qualification & Validation (CQV) fundamentals.
• Good Documentation Practices (GDPs) and SOP creation.
• Knowledge of GMP-regulated environments (life sciences / pharmaceutical manufacturing).
• Ability to read process/facility drawings and validate equipment installations.
• Microsoft Office suite proficiency.
• Strong problem-solving, teamwork, and client-facing skills.

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Why Careertakes & This Opportunity

• Third-party recruiting support with access to additional matched roles via Careertakes.
• Structured mentorship and on-the-job learning with experienced CQV professionals.
• Work on impactful, regulated life-sciences projects that support GMP manufacturing.

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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.