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.
Job Responsibilities
* 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.
Qualifications
* 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.
Why Join Us?
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.
Required Skills
* Good Manufacturing Practices (GMP)
* Stakeholder Collaboration
* Sterile Compounding
Seniority level
Not Applicable
Employment type
Full‑time
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