Process Engineer

We are seeking a motivated Entry‑Level Process Engineer to support manufacturing operations, process optimization, and continuous improvement initiatives in a GMP‑regulated pharmaceutical or medical device environment. The ideal candidate will work closely with Manufacturing, Quality, and Engineering teams to improve process efficiency and ensure product quality.

• Assist in monitoring and optimizing manufacturing processes
• Support process validation activities, including IQ, OQ, and PQ
• Investigate process deviations and support root cause analysis
• Develop and update SOPs, work instructions, and process documentation
• Collaborate with Manufacturing, Quality, and Validation teams on process improvements
• Collect and analyze process data to identify opportunities for efficiency improvements
• Support equipment qualification and manufacturing scale‑up activities
• Ensure compliance with GMP, FDA regulations, and company quality standards

• Bachelor's degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, Biomedical Engineering, or related field
• 0–2 years of experience in process engineering, manufacturing, or internships in regulated industries
• Basic understanding of manufacturing processes and engineering principles
• Knowledge of GMP/cGMP and quality systems is a plus
• Strong analytical, problem‑solving, and communication skills
• Proficiency with Microsoft Office (Excel, Word, PowerPoint)

• Exposure to pharmaceutical, biotechnology, or medical device manufacturing
• Familiarity with Lean Manufacturing or Six Sigma concepts
• Knowledge of validation documentation and change control processes
• Experience with AutoCAD or data analysis tools is a plus