Process Engineer (Large Molecules)

Actalent; Basel; Vor Ort; CHF 95.000 - 130.000; Vollzeit

Zusammenfassung

Actalent is seeking a Process Engineer / Operations Engineer to join its Operations Engineering team in Basel to support construction and commissioning of a new facility.

The role blends process optimization for pharmaceutical and biotech manufacturing, with emphasis on utility systems, cGMP compliance, and project execution from concept to handover. Fluent German and strong English communication are required.

Qualifikationen

• Bachelor or master’s degree in engineering or related technical discipline.
• 2–5+ years of experience in Drug Substance and Large Molecules or GMP-regulated environments.
• Fluent German with strong English communication skills.

Aufgaben

• Develop, implement, and optimize process engineering solutions in pharmaceutical and biotech facilities.
• Support construction, commissioning, and operational readiness of new utility and manufacturing infrastructure.
• Ensure project delivery within timelines, budgets, and technical objectives.

Kenntnisse

German language

English communication

Team player

Ausbildung

Engineering degree or related technical discipline

Tools

Microsoft Office

Google Workspace

Jobbeschreibung

Our client is seeking a Process Engineer / Operations Engineer to join its Operations Engineering team and support the construction and commissioning of a new facility.

This role combines operational and project engineering responsibilities, with a focus on process optimization, utility systems, and supporting complex pharmaceutical and biotechnological manufacturing operations.

Responsibilities:

• Develop, implement, and optimize process engineering solutions within pharmaceutical and biotechnological production facilities.
• Support the construction, commissioning, and operational readiness of new utility and manufacturing infrastructure.
• Ensure project delivery in line with agreed timelines, budgets, and technical objectives.
• Maintain compliance with cGMP requirements across operational engineering activities and investment projects.
• Provide technical support for complex chemical and biotechnological manufacturing plants.
• Lead and support plant optimization and modification initiatives to improve performance and reliability.
• Manage investment projects throughout the full lifecycle, from initial concept and design through execution and handover to operations.
• Support active pharmaceutical ingredient (API) production processes, including both batch and continuous manufacturing.
• Collaborate closely with cross-functional project teams in an interdisciplinary engineering environment.

Must-Haves:

• University degree in Engineering or a related technical discipline, or an equivalent qualification.
• 2-5 + years of experience in Drug Substance and Large Molecules
• Initial professional experience within the pharmaceutical, biotech, or GMP-regulated industry.
• Strong general IT skills, including proficiency with Microsoft and Google applications.
• Fluent German and good English communication skills, both written and spoken.
• Positive, proactive, and team-oriented personality with strong interpersonal skills.

Preferred Qualifications:

• Experience with ultrapure media, steam, and energy systems.
• Process engineering expertise related to utility systems.
• Knowledge of system design, including pumps and heat exchangers.