Process Engineering Consultant

Process Design & Engineering: Develop process engineering deliverables including process flow diagrams, process descriptions, equipment specifications, calculations, and technical reports.

Project Execution: Execute assigned engineering tasks throughout conceptual, basic, and detailed design phases while meeting project quality, budget, and schedule expectations.

Technical Collaboration: Work closely with multidisciplinary project teams, clients, vendors, and subject matter experts to develop practical and compliant process solutions.

Problem Solving & Analysis: Analyze technical challenges, evaluate alternatives, and recommend effective solutions to support client objectives and project success.

Continuous Improvement: Contribute to knowledge sharing, process improvements, and best practices that enhance project delivery and customer value.

Willingness and ability to be based in Clayton, working in an agile, fast-paced, project-oriented environment that supports both customers and colleagues.

Bachelor or Master's degree in Chemical Engineering, Biochemical Engineering, Biotechnology, Pharmaceutical Engineering, or a related engineering discipline.

Minimum 3 years of relevant engineering experience within pharmaceutical, biotechnology, life sciences, or related regulated industries.

supporting process design activities including process calculations, PFDs, P&IDs, equipment sizing, and technical documentation.

Familiarity with GMP-regulated environments and pharmaceutical manufacturing processes.

Enjoy collaborating with multidisciplinary teams to solve technical challenges and deliver high-quality engineering solutions.

Demonstrate strong communication skills and the ability to build productive relationships with customers and project teams.

Possess a proactive mindset, strong attention to detail, and a commitment to continuous improvement.

Continuously expand technical capabilities through project experience, learning opportunities, and feedback.

with commissioning, qualification, validation, or process optimization activities is a plus. What We Offer You Competitive salary with annual adjustment increases 160 hours of PTO (prorated from hire date) + 14 paid holidays Health, dental, and vision insurance from day one 8% guaranteed 401(k) company contribution 14 weeks paid parental leave Company-paid life and disability insurance Employee referral bonuses

• Willingness and ability to be based in Clayton, working in an agile, fast-paced, project-oriented environment that supports both customers and colleagues.
• Bachelor or Master's degree in Chemical Engineering, Biochemical Engineering, Biotechnology, Pharmaceutical Engineering, or a related engineering discipline.
• Minimum 3 years of relevant engineering experience within pharmaceutical, biotechnology, life sciences, or related regulated industries.
• Experience supporting process design activities including process calculations, PFDs, P&IDs, equipment sizing, and technical documentation.
• Familiarity with GMP-regulated environments and pharmaceutical manufacturing processes.
• Enjoy collaborating with multidisciplinary teams to solve technical challenges and deliver high-quality engineering solutions.
• Demonstrate strong communication skills and the ability to build productive relationships with customers and project teams.
• Possess a proactive mindset, strong attention to detail, and a commitment to continuous improvement.
• Continuously expand technical capabilities through project experience, learning opportunities, and feedback.
• Experience with commissioning, qualification, validation, or process optimization activities is a plus.

• Competitive salary with annual adjustment increases
• 160 hours of PTO (prorated from hire date) + 14 paid holidays
• Health, dental, and vision insurance from day one
• 8% guaranteed 401(k) company contribution
• 14 weeks paid parental leave
• Company-paid life and disability insurance
• Employee referral bonuses

Please submit your application online.

Please note that we only accept applications submitted via our online system.

This position is not eligible for employer-sponsored work authorization.

Candidates must have unrestricted authorization to work in the United States and must not require current or future sponsorship to maintain that authorization.

Deadline of application is 9/25/2026

We will invite to interviews on a running basis.