Acceptance Testing, Biotech and Pharmaceutical, C Programming Language, Capital Project, Commissioning, Construction Engineering, Data Quality, Documentation Plan, Documentation Standards, Drug Products, Embedded Systems, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), Manufacturing, Manufacturing Operations, Manufacturing Systems, Manufacturing/Industrial Processes, Regulations, Requirements Management, System Operations, Systems Administration/Management, Test Scripts, Writing Skills
Hello,
I hope you're doing well.
My name is Jayadev, and I'm reaching out from Intellectt Inc. regarding an exciting contract opportunity for a C&Q Engineer Based in Ohio,with one of our prestigious clients.
I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at jayadev.g@intellectt.com
Title: C&Q Engineer
Location: Ohio 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 2Develop, 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
Thanks Regards,
JAYADEV
Sourcing Specialist
Phone (732)-997-6982 Ext: 308
Email jayadev.g@intellectt.com