CQV Engineer - Basel, Switzerland - German Speaking - Contract

Optimus Life Sciences; Basel; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Zusammenfassung

Optimus Life Sciences is supporting a Swiss engineering organisation with an expanded pharma project load, seeking experienced Commissioning & Qualification Engineers to join the team in Basel and at customer sites worldwide.

The role is hands-on, focusing on IQ/OQ, commissioning of automated pharmaceutical equipment, and documentation in GMP-compliant records. You will collaborate across engineering and QA teams and travel internationally for site testing.

Qualifikationen

• Experience in commissioning/CQV in GMP environments.
• Strong automation and PLC understanding.
• Experience with IQ/OQ and commissioning protocols.
• Ability to travel internationally for commissioning work.
• Excellent GMP documentation practices.

Aufgaben

• Execute commissioning and qualification activities on automated pharmaceutical equipment.
• Perform I/O checks, signal testing and functional testing.
• Execute predefined IQ/OQ and commissioning protocols.
• Support testing of automation and control systems on site.
• Review equipment against technical documentation and specifications.
• Identify and troubleshoot mechanical, electrical and automation issues.
• Maintain accurate GMP documentation throughout testing and qualification.
• Collaborate with internal teams and customer's sites during delivery.

Kenntnisse

CQV experience

GMP knowledge

I/O checks

Qualification protocols

Siemens PLC

Tools

Siemens PLC

Jobbeschreibung

Optimus Life Sciences are supporting a Swiss engineering organisation with an increased volume of pharmaceutical projects and are looking for experienced Commissioning & Qualification Engineers to strengthen their team.

This is a hands-on position supporting the testing and qualification of automated pharmaceutical equipment, with work split between the Basel area and customer sites internationally.

Responsibilities

• Execute commissioning and qualification activities on automated pharmaceutical equipment
• Perform I/O checks, signal testing and functional testing
• Execute predefined IQ/OQ and commissioning protocols
• Support testing of automation and control systems
• Review equipment against technical documentation and specifications
• Identify and troubleshoot mechanical, electrical and automation-related issues
• Complete accurate GMP documentation throughout testing and qualification
• Support both internal testing and commissioning activities at customer sites
• Work closely with engineering, automation and qualification teams through project delivery

Requirements

• Previous Commissioning / CQV experience within GMP-regulated environments
• Good understanding of automation and PLC-controlled equipment
• Siemens PLC experience highly advantageous
• Experience with I/O checks, functional testing and qualification protocols
• Strong understanding of GMP documentation requirements
• Comfortable working hands-on with pharmaceutical equipment
• Willingness to travel internationally for commissioning activities
• English – professional working proficiency
• Available for a freelance/contract assignment