About this role

For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a Process/Operations Engineer.

General Information:

Start Date: 02.02.2026
Latest Possible Start Date: 02.03.2026
Planned Employment Duration: until 30.09.2026 with the possibility of extension
Workplace: Basel
Workload: 100%
Team: 20 team members
Department: Pharma Engineering Drug Substance
Working Hours: Standard

About the job:

The Pharma Engineering Drug Substance Small Molecules division ensures the technical support and further development of the production facilities for the manufacture of chemical active ingredients at the site in Basel. They work in self-organized teams. This means a move away from rigid hierarchies towards a high degree of personal responsibility and collaborative coordination. Success in this position requires proactive action, independent task management, and active teamwork. They are looking for individuals who think entrepreneurial and communicate decisions transparently. This position is initially vacant to temporarily strengthen the team and cover project peaks. If the collaboration is successful and the need arises, there is a clear possibility of long-term, external employment.

Your Profile:

The ideal candidate will hold a degree in process engineering or a related field and have more than five years of experience in a GMP environment.

Tasks & Responsibilities:

1. Engineering & Technical Planning:

R&I Processing: Independent processing and maintenance of P&IDs in COMOS and ensuring data consistency
Design Documentation (DQ): Creation of technical specifications, data sheets, and technical drawings as a basis for execution
Isometrics: Technical review and approval of isometrics and manufacturing documents from the pipeline construction companies.

2. Project Management & Implementation (Construction):

Trade Coordination: Management and coordination of the various trades (pipeline construction, instrumentation and control, automation, construction) for the planning, execution, and commissioning phases.
Construction Management: On-site support of the implementation to ensure assembly quality and compliance with safety regulations.
Resource Management: Ensuring that small projects are completed within the agreed scope, quality, budget, and deadlines.

3. GMP Compliance, Qualification & Change Management:

Change Control: Definition and establishment of all necessary measures (organizational, technical, documentation) for the successful and compliant implementation of a change.
Verification (IQ/OQ): Creation of acceptance documentation (test plans, protocols) for verifying the installations and support during acceptance testing.
Documentation: Compilation of the complete "as-built" documentation and handover to the operator.

Must Haves:

Completed technical or scientific degree (University of Applied Sciences/University/ETH) in Process Engineering, Chemical Engineering, Pharmaceutical Engineering or comparable field / completed advanced vocational training (Diploma Technician HF) with several years of relevant professional experience
At least 5 years of experience in a GMP environment. You are thoroughly familiar with the regulations and requirements of pharmaceutical production
Proficient use of standard PC applications. Experience with specific systems (SAP, myBuy, ELIVS/COMOS) is a significant advantage
Excellent written and spoken German skills are essential for documentation and communication within the company
You work independently and are able to proactively identify tasks and handle them transparently.
You are part of an interdisciplinary team and contribute to shared success through cooperation and communication.
You have a sense of urgency, can effectively prioritize tasks, and take responsibility.
Ability to write precise, technical texts and document efficiently.

Nice to have: