Sr Process Engineer (Mechanical Systems) – Radioisotope Manufact

Role Summary

Key Responsibilities

• Lead the design, procurement, installation, commissioning, qualification, and continuous improvement of fixtures, tooling, equipment, and process systems.
• Develop process flow diagrams (PFDs), Piping & Instrumentation Diagrams (P&IDs), equipment layouts, and engineering specifications.
• Create detailed engineering drawings, 3D models, and Bills of Materials (BOMs) using CAD software.
• Support preventive and predictive maintenance programs to maximize equipment performance and uptime.
• Partner with R&D teams to transfer new radioisotope manufacturing processes into commercial GMP operations.
• Prepare User Requirement Specifications (URS), Functional Design Specifications (FDS), and related engineering documentation.
• Support equipment qualification activities, including FAT, SAT, IQ, OQ, and PQ protocols.
• Manage engineering change controls and contribute to validation activities.
• Develop and maintain SOPs, maintenance procedures, and engineering standards.
• Provide technical support for manufacturing operations, investigations, troubleshooting activities, and regulatory inspections.
• Drive continuous improvement initiatives focused on safety, quality, efficiency, and reliability.

Required Qualifications

• Bachelor's or Master's degree in Mechanical Engineering, Manufacturing Engineering, Bioengineering, or a related engineering discipline.
• 3-5 years of experience in fixture design, process development, process optimization, validation, or related engineering functions.
• Proficiency with CAD software such as SolidWorks for creating 3D models and 2D engineering drawings.
• Strong understanding of mechanical systems, fluid mechanics, heat transfer, and process equipment design.
• Knowledge of engineering change management and document control systems.
• Strong troubleshooting, technical problem-solving, and root cause analysis skills.
• Excellent written and verbal communication skills.
• Ability to collaborate effectively within multidisciplinary teams.

Preferred Qualifications

• Experience designing and installing automated manufacturing systems or production lines.
• Experience working in highly regulated manufacturing environments, including pharmaceutical, medical device, biotechnology, or radiopharmaceutical industries.
• Knowledge of GMP manufacturing practices and validation requirements.
• Experience supporting qualification and commissioning activities for manufacturing equipment and facilities.
• Familiarity with radiopharmaceutical manufacturing or radioactive material handling environments.

Work Environment

Career Growth

Innovative Projects

Collaborative Culture

Competitive Benefits

• Enjoy a comprehensive benefits package designed to support your professional success, health, and well-being.

Purpose-Driven Work

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