Senior Process Engineer II - OSD and Packaging

Takeda • Lexington, MA

1d • Onsite

About The Position

Join Takeda’s growing Lexington, MA manufacturing site as a Senior Process Engineer II, where you will help deliver life‑changing medicines to patients through the design, start‑up, operation, and optimization of oral solid dosage and packaging manufacturing equipment. This is a highly visible, on‑site role within the Process Engineering organization, supporting the Oral Solid Dosage and Packaging design‑build project as well as start‑up and long‑term commercial manufacturing operations at the Lexington site. In this role, you will serve as a technical subject matter expert for manufacturing unit operations, playing a critical role in ensuring safe, compliant, and reliable production while driving process efficiency and continuous improvement. You thrive at the intersection of engineering and operations, enjoy hands‑on problem solving on the shop floor, and value close collaboration with equipment vendors, operators, and technical peers. You are motivated by seeing improvements translate directly into meaningful production impact.

Requirements

• Bachelor’s degree in Engineering (Chemical, Mechanical, Process, or related discipline) with a minimum of 10 years of relevant industry experience.
• Proven experience supporting oral solid dosage manufacturing equipment, including milling, blending, granulation, drying, compression, coating, and packaging (strongly preferred).
• Strong technical problem‑solving capability, with the ability to lead cross‑functional troubleshooting efforts and drive successful project execution.
• Hands‑on experience working in cGMP pharmaceutical or other regulated manufacturing environments.
• Demonstrated ownership of equipment performance, with a track record of driving continuous improvement and serving as a trusted technical subject matter expert.
• Excellent communication and collaboration skills, with the ability to effectively engage engineering, manufacturing, quality, and cross‑functional stakeholders at all levels of the organization.

Responsibilities

• Serve as a Process Engineering subject matter expert (SME), applying Good Engineering Practice (GEP) principles to the design, build, and testing of manufacturing unit operations within your scope. You will partner closely with Manufacturing, Manufacturing Sciences, Facilities, Global Engineering, Quality, and cross‑functional project teams.
• Lead and execute start‑up, commissioning, and validation activities for new equipment and processes supporting cGMP operations, including milling, sieving, IBC handling, roller compaction, fluid bed drying, tablet compression, coating, packaging, and CIP/COP systems.
• Support day‑to‑day manufacturing operations by maintaining and continuously improving equipment performance and reliability, serving as the primary technical point of contact for your assigned area.
• Drive effective troubleshooting and root‑cause analysis, supporting deviation investigations, closure activities, and the implementation of corrective and preventive actions (CAPAs).
• Develop, review, and sustain technical and GMP documentation, including SOPs, specifications, and engineering assessments, ensuring alignment with global standards and regulatory expectations.

Benefits

• Comprehensive Healthcare: Medical, Dental, and Vision
• Financial Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan
• Health & Wellness programs including onsite flu shots and health screenings
• Generous time off for vacation and the option to purchase additional vacation days
• Community Outreach Programs and company match of charitable contributions
• Family Planning Support
• Flexible Work Paths
• Tuition reimbursement

What This Job Offers

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