Lead Process Engineer, Pharma Manufacturing Startup

Serán BioScience; Bend (OR); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Over four weeks of paid time off annually

Employer contributions to retirement account after 90 days

Health plans with minimal employee contributions

Basic life and long-term disability coverage

Employee Assistance Program

Job summary

Serán BioScience is seeking a Process Engineer in Bend, Oregon, to ensure compliance with cGMP standards in our new commercial manufacturing operations. This position involves leading start-up, commissioning, and continuous improvement projects to enhance production efficiency.

The ideal candidate will have 8+ years of relevant experience, a BS/MS in engineering, and hands-on expertise in pharmaceutical manufacturing processes. Competitive benefits include over four weeks of paid time off annually and health coverage.

Qualifications

• 8+ years of experience in pharmaceutical manufacturing, process engineering, or industrial engineering.
• Hands-on experience with facility start-up, commissioning, and equipment qualification.
• Strong knowledge of cGMP requirements and commercial manufacturing operations.

Responsibilities

• Lead design and engineering activities associated with process equipment for new installations.
• Design and refine commercial-scale manufacturing processes for oral solid dosage forms.
• Drive readiness activities for commercial launch, including supporting process validation.

Skills

Process modeling

Workflow analysis

Lean/Six Sigma tools

Communication skills

Documentation skills

Education

BS/MS in Industrial Engineering, Chemical Engineering, Mechanical Engineering, or related discipline

Job description

Serán BioScience is seeking a Process Engineer in Bend, Oregon, to ensure compliance with cGMP standards in our new commercial manufacturing operations. This position involves leading start-up, commissioning, and continuous improvement projects to enhance production efficiency.

The ideal candidate will have 8+ years of relevant experience, a BS/MS in engineering, and hands-on expertise in pharmaceutical manufacturing processes. Competitive benefits include over four weeks of paid time off annually and health coverage.