Mandatory Skills:
• BS/MS Degree in Chemical Engineering, Mechanical Engineering, or related field
• PE License Preferred
• 8+ years of mixed engineering & manufacturing experience, primarily in the biopharmaceutical industry
• Process Engineering experience within FDA Regulated Settings for Pharmaceutical, Biotech, or Life-Sciences.
• The Process Engineer will work within the CQV Group to support the overall engineering team by understanding and assessing client process needs, including the infrastructure impacts of these needs, as well as designing GMP compliant equipment and systems.
• Work on projects primarily in the biopharmaceutical sector, and include manufacturing processes (e.g., biological, API, oral solid dosage, cell therapy) and support systems (e.g., clean utilities, CIP, buffer and media preparation, waste inactivation and treatment).
• Prepare scope and hourly estimates for various process work in preparation of client proposals.