Process Engineer Parenterals NPI​/LCM

Staff Process Engineer Parenterals NPI/LCM

Johnson & Johnson Innovative Medicine

Location:

Schaffhausen, Switzerland

We are looking for a Staff Process Engineer to join our Parenterals Manufacturing and Filling Operations organization. The role focuses on introducing new products in commercial production, implementing new technologies, and ensuring robust process implementation.

• Execution and support of projects in New Product Introduction and Lifecycle Management in the Business Unit Parenterals.
• Execution and support of improvement projects.
• Responsible for change controls, recipe and document changes.
• Handling of quality investigations concerning process and material deviations.
• Training of project related content on the shop floor and in the leadership teams.
• Acts as Subject Matter Expert in project related audits.
• Close collaboration with production and other relevant business partners.
• Follow GMP, EHS and SOX guidelines.

• Minimum bachelor’s degree in natural science or engineering;
  Master’s degree preferred.
• 4+ years of experience in the Pharmaceutical industry with at least 2 years in a role involving parenteral/pharmaceutical manufacturing or development.
• Experience with introduction of parenteral products into manufacturing sites and technical/process knowledge of unit operations such as compounding, milling, and filling of liquid formulations and suspensions.
• Strong planning and logistics skills to integrate drug product deliverables.
• Knowledge of manufacturing site systems and procedures (e.g., SAP, PAS-X).
• Excellent written and oral communication skills and ability to influence partners, peers, and collaborators at all levels.
• Proficiency in German and English required.
• Ability to work independently with proven problem‑solving skills.

Become part of a forward‑thinking company committed to excellence in pharmaceutical manufacturing. In this role, you will work in a collaborative environment and make a lasting impact on innovative processes.

• Good Manufacturing Practices (GMP)
• Stakeholder Collaboration
• Sterile Compounding

Not Applicable

Full‑time