Commissioning & Qualification Engineer

Intellectt Inc; New Albany (OH); On-site; USD 61,992 - 68,880; Full time

Job summary

Intellectt Inc is seeking a Commissioning & Qualification (C&Q) Engineer in New Albany, Ohio, to lead C&Q activities for a major expansion project involving new packaging lines. This hands-on role demands expertise in commissioning and qualification within a regulated pharmaceutical environment.

The selected candidate will be responsible for ensuring all systems are installed and verified before transitioning to GMP manufacturing. A strong understanding of equipment commissioning and process knowledge is required for compliance with FDA and GMP standards.

Qualifications

• Experience in a regulated pharmaceutical environment.
• Ability to manage punch list identification and resolution.
• Strong collaboration skills with vendors and operations teams.

Responsibilities

• Lead and execute the C&Q activities for new equipment.
• Develop and review C&Q documentation.
• Perform equipment walkdowns and system verifications.
• Manage system acceptance and turnover.

Skills

Deep expertise in equipment commissioning

Knowledge of manufacturing processes in pharmaceuticals

Ability to develop and execute C&Q documentation

Hands-on equipment verification skills

Job description

Title: Commissioning & Qualification (C&Q) Engineer

Location: New Albany, Ohio

Duration: 06 months+

Pay rate: $45-$50/hr on W2

Job Description :

We are looking for an experienced Commissioning & Qualification (C&Q) Engineer to join our team in support of a major capital expansion project involving the installation of four new packaging lines. This is a hands‑on C&Q role embedded within a pharmaceutical secondary and tertiary packaging operation for final drug product. This is not a validation role — we are looking for a true C&Q professional with deep expertise in equipment commissioning, system turnover, and manufacturing process knowledge within a regulated pharmaceutical environment.

You will be responsible for leading and executing commissioning and qualification activities across new packaging equipment installations, ensuring all systems are built, installed, and functionally verified to specification and ready for handover to GMP manufacturing operations.

Key Responsibilities:

• Lead and execute commissioning and qualification activities for new secondary and tertiary packaging equipment installations across four new packaging lines in Building 2
• Develop, author, review, and execute C&Q documentation including commissioning plans, commissioning protocols, test scripts, punch lists, and turnover packages
• Perform hands‑on equipment walkdowns, system verifications, and commissioning checks directly on the manufacturing floor
• Manage punch list identification, tracking, and resolution through to system acceptance and turnover
• Collaborate with equipment vendors, engineering, construction, and operations teams to ensure systems are installed, functional, and commissioned to design specification
• Support and execute SAT (Site Acceptance Testing) activities for incoming packaging equipment
• Ensure all C&Q activities are performed in compliance with FDA, GMP, and applicable site and regulatory standards
• Apply manufacturing process knowledge to ensure commissioning scope and acceptance criteria reflect real‑world operational requirements
• Partner with Quality, Manufacturing, and Engineering to support a clean, compliant turnover of commissioned systems into GMP operations
• Maintain accurate and complete C&Q records in compliance with site documentation standards and data integrity requirements