Title: Process Engineer
Location: Rockford, IL
Duration: 6-12 months
Key Responsibilities:
• Develop and define process specifications and parameters for new and existing products.
• Support validation activities, including IQ/OQ/PQ and process qualification.
• Create and update technical documentation such as protocols, reports, and risk assessments.
• Analyze process data and trends to identify areas for improvement and cost-saving opportunities.
• Collaborate with Quality, Manufacturing, and R&D teams to ensure process reliability and compliance.
• Participate in root cause investigations and implement CAPA actions as needed.
Qualifications:
• Bachelor’s degree in Engineering, Life Sciences, or related field.
• Experience in process engineering and validation within regulated industries (e.g., pharma, biotech).
• Familiarity with GMP, FDA, and ISO standards.
• Strong documentation and technical writing skills.