C&Q Engineer at Techtrueup

New Albany, Ohio, United States -

Full Time

Start Date

Immediate

Expiry Date

26 Aug, 26

Salary

0.0

Posted On

28 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Commissioning, Qualification, Equipment Installation, SAT, GMP, FDA Compliance, System Turnover, Technical Writing, Punch List Management, Pharmaceutical Packaging, Manufacturing Process Knowledge, Data Integrity

Industry

Human Resources Services

Description

Company Description Fusion Life Sciences Technologies (www.fusionlifesolutions.com ) is a WBE-certified Healthcare Staffing and Engineering Services provider supporting industries including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food & Beverage, and Automotive. We proudly partner with 120+ clients such as Johnson & Johnson, Haemonetics, Delta, Caterpillar, Artisan Chef, Baxter, and many more. Our wide network of consultants and contract-to-hire engineers brings deep expertise across Engineering, Technical, Administrative, Healthcare, Life Sciences, Blue Collar, Skilled Trades, IT, Software Development, Manufacturing, and Supply Chain sectors. What sets us apart is our AI-powered, in-house software's enabling us to source and screen top talent within hours. This ensures rapid response times, high-quality matches, and virtually zero attrition. Job Description Title: Commissioning & Qualification (C&Q) Engineer Location: Ohio Duration: 6 months Shift: 1st shift (7:00am – 4:00pm) | 2nd shift (3:00pm – 11:00pm) 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. Additional Information All your information will be kept confidential according to EEO guidelines.

Responsibilities

Lead and execute commissioning and qualification activities for new secondary and tertiary packaging lines in a pharmaceutical environment. Develop and execute C&Q documentation and manage the turnover of systems into GMP operations.