Engineering SME

Eliquent Life Sciences, Inc • Costa Mesa, CA

5h • $100 - $130

About The Position

The Engineering Subject Matter Expert (SME) plays a critical role in bridging advanced engineering principles with pharmaceutical manufacturing processes to ensure efficient, compliant, and innovative production operations. This position is responsible for providing expert guidance on the design, implementation, and optimization of pharmaceutical equipment and manufacturing workflows, leveraging deep knowledge of architectural design software and industry best practices. The SME collaborates closely with cross-functional teams including production, quality assurance, and R&D to drive continuous improvement and troubleshoot complex technical challenges. By integrating engineering expertise with regulatory and safety standards, the SME ensures that manufacturing processes meet stringent quality and compliance requirements. Ultimately, this role contributes to the successful delivery of high-quality pharmaceutical products while supporting scalable and sustainable manufacturing solutions across the organization.

Requirements

• Bachelor’s degree in Engineering, Pharmaceutical Engineering, or a related technical field.
• Proven experience with architectural design software relevant to manufacturing facility planning.
• Demonstrated knowledge of pharmaceutical manufacturing processes and equipment operation.
• Strong understanding of regulatory requirements and quality standards in pharmaceutical manufacturing.
• Excellent problem-solving skills and ability to communicate complex technical information clearly.

Nice To Haves

• Master’s degree in Engineering or related discipline.
• Experience working within a pharmaceutical manufacturing environment.
• Certification in project management or process improvement methodologies (e.g., Six Sigma).
• Familiarity with automation and control systems used in pharmaceutical production.
• Previous experience in cross-functional team leadership or training roles.

Responsibilities

• Lead the design and review of pharmaceutical manufacturing equipment layouts and facility architectural plans using advanced design software.
• Provide technical expertise and support for the operation and maintenance of pharmaceutical manufacturing equipment to optimize performance and reliability.
• Collaborate with manufacturing, quality, and regulatory teams to ensure processes comply with industry standards and regulatory requirements.
• Analyze and troubleshoot engineering issues related to pharmaceutical production processes, recommending and implementing effective solutions.
• Develop and deliver training and documentation to internal teams on best practices for equipment operation and process optimization.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior