Senior Tech Transfer Engineer

Consultant – Engineering Specialist | Harba Solutions Indianapolis

Base pay range: $/yr – $/yr

Direct message the job poster from Harba Solutions Inc.

• Provide technical support for the manufacturing of oral solid dosage (OSD) forms, ensuring processes are efficient, compliant, and meet quality standards.
• Support technology transfer activities by collaborating with cross‑functional teams to introduce new processes and products into commercial manufacturing.
• Identify, troubleshoot, and resolve technical issues related to equipment, processes, and materials to minimize downtime and ensure consistent production.
• Lead and participate in continuous improvement initiatives focused on process efficiency, product quality, and cost optimization.
• Author, review, and maintain technical documentation including batch records, standard operating procedures (SOPs), and technical reports.
• Ensure manufacturing activities comply with applicable regulatory requirements, current Good Manufacturing Practices (cGMP), and internal quality systems.
• Analyze process and manufacturing data to identify trends, optimize performance, and support data‑driven decision‑making.
• Collaborate with Manufacturing, Quality Assurance, Quality Control, Supply Chain, Process Development, and other functional teams to support ongoing operations and implementation of new technologies or improvements.

• Bachelor’s degree in Engineering, Pharmaceutical Sciences, or a related technical discipline.
• 5–10 years of experience in pharmaceutical manufacturing with a strong technical focus on oral solid dosage forms.
• In‑depth knowledge of OSD manufacturing processes, equipment, and technologies.
• Experience with data analysis and process optimization tools; familiarity with JMP statistical software and coding in JSL, SQL, Java, HTML, and/or Python is preferred.
• Strong troubleshooting, analytical, and problem‑solving skills.
• Excellent written and verbal communication skills with the ability to work effectively across technical and non‑technical teams.
• Working knowledge of cGMPs, FDA regulations, and applicable pharmaceutical industry standards.

Mid‑Senior level

Full‑time

Engineering, Manufacturing, and Project Management

Pharmaceutical Manufacturing, Health and Human Services, Medical Equipment Manufacturing