What are the responsibilities and job description for the Project manager position at Fusion Life Sciences?
Industry: Pharmaceutical / Biopharmaceutical
Work Authorization: U.S. Citizens Only
Educational Background: Mechanical Engineering or Civil Engineering
Key Expertise: Equipment Assembly, Commissioning & Qualification (C&Q)
Location: Columbus Ohio
Interview: Virtual
We are seeking an experienced Equipment Assembly & Commissioning Engineer with a pharmaceutical industry background to support the assembly, installation, commissioning, and qualification of manufacturing equipment in a regulated pharmaceutical environment. The ideal candidate will have a Mechanical or Civil Engineering background and knowledge of Commissioning and Qualification (C&Q) processes, GMP requirements, and equipment documentation.
Key ResponsibilitiesSupport the assembly, installation, and setup of pharmaceutical manufacturing equipment and associated systems.
Coordinate equipment installation and commissioning activities in accordance with approved engineering specifications and project requirements.
Support Commissioning and Qualification (C&Q) activities, including equipment verification, functional testing, and qualification documentation.
Assist with developing, executing, and reviewing commissioning and qualification protocols, test records, and reports.
Verify equipment functionality, installation readiness, and compliance with design specifications and operational requirements.
Identify equipment assembly issues, installation discrepancies, and technical problems; coordinate troubleshooting and resolution.
Collaborate with Engineering, Manufacturing, Quality Assurance, Validation, and project teams to ensure successful equipment implementation.
Maintain accurate engineering documentation, equipment records, and commissioning/qualification deliverables.
Ensure work is performed in accordance with applicable GMP requirements, safety procedures, and pharmaceutical quality standards.
Support equipment handover and readiness for manufacturing operations.
Bachelor’s degree in Mechanical Engineering or Civil Engineering.
Experience working in the pharmaceutical or biopharmaceutical industry.
Knowledge of equipment assembly, installation, commissioning, and qualification activities.
Familiarity with C&Q methodologies and equipment qualification documentation.
Understanding of GMP requirements and regulated manufacturing environments.
Strong troubleshooting, documentation, coordination, and problem-solving skills.
Ability to collaborate with multidisciplinary engineering and quality teams.
Must be a U.S. citizen.
Hands-on experience with pharmaceutical manufacturing equipment installation and assembly.
Experience with commissioning and qualification protocols, functional testing, and equipment acceptance activities.
Familiarity with IQ/OQ and equipment qualification documentation.
Exposure to pharmaceutical facility projects, equipment startup, and operational readiness.
Knowledge of engineering drawings, equipment specifications, and installation requirements.
Pharmaceutical Manufacturing | Equipment Assembly | Equipment Installation | Commissioning & Qualification (C&Q) | IQ/OQ | GMP | Equipment Qualification | Functional Testing | Engineering Documentation | Troubleshooting | Mechanical Systems | Project Coordination
Bill Rate: $70/hour
Candidate Profile: U.S. citizen with a Mechanical or Civil Engineering background, pharmaceutical industry experience, and C&Q knowledge.
Salary : $70