Project Qualification Engineer (Pharma Engineering Solids)

Posted on July 15, 2026
Basel
English
Temporary
Posted on July 15, 2026

About this role

For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for an Operations / Project Qualification Engineer in Pharma Engineering Solids.

General Information:

  • Start Date: ASAP
  • Latest possible start date: 01.10.2026
  • Planned Employment Duration: unlimited
  • Workplace: Basel and Kaiseraugst
  • Workload: 80-100%
  • Home Office: possible, max 1 day per week
  • Travel: only as needed, e.g., for FATs (Factory Acceptance Tests)
  • Team Size: 20 People
  • Department: Chapter Business Solutions (EFHCD)
  • Working Hours: Standard


About the job:

The Drug Product Qualification department is looking for a Qualification Expert for independent operations engineering activities and project work in the Drug Product area in Basel and Kaiseraugst.

The production facilities consist of the following machines and systems:

  • Filling machines (Liquid/Solids), encapsulation, tableting, granulation, labeling machines, inspection machines, assembly lines for syringes & autoinjectors, equipment washing machines, autoclaves, etc.
  • Infrastructure systems: Cold rooms, cleanrooms, HVAC (heating, ventilation, air conditioning), compressed air, process air, WFI (Water for Injection) distribution, environmental monitoring, etc.

The Perfect Candidate:

Possesses a completed vocational training or a degree in fields such as automation, mechanical engineering, process engineering, pharmaceutical technology, or biotechnology. Furthermore, a minimum of 5 years of professional experience in the qualification of automated pharmaceutical production equipment as well as sound knowledge of the GMP-regulated environment is required. Additional requirements include practical experience in implementing technical GMP specifications of regulatory authorities (Swissmedic, FDA, EMA) in investment projects and operations engineering. A structured, precise way of working as well as high social competence and the ability to communicate complex matters in a target-group-oriented manner are essential for this position. Very good German and English language skills are mandatory.

Tasks & Responsibilities:

  • Execution and support of qualification activities in investment projects.
  • Writing and executing qualification plans and reports.
  • Reviewing supporting documentation for GMP compliance and fulfillment of acceptance criteria.
  • Creating, tracking, and closing qualification action items/pendings.
  • Maintaining inventory data of the qualified systems/equipment.
  • Collaborative partnership with interface departments.
  • Presenting qualification topics during inspections, answering inspection questions, and maintaining the contact person matrix.
  • Assessing and evaluating the impact of changes and deviations on the qualified status and critical aspects.
  • Carrying out (re-)qualification measures resulting from changes and deviations.
  • Planning and conducting periodic qualification reviews.
  • Approving technical planning documents.
  • Assuming inventory responsibility.


Must-Haves:

  • Completed education/training or degree in one of the following fields: Automation, Mechanical Engineering, Process Engineering, Pharmaceutical Technology, Biotechnology
  • Min. 5 years of professional experience in the qualification of automated pharmaceutical production (Drug Product)
  • Professional experience in a GMP-regulated working environment
  • Neat, structured, and precise way of working.
  • High social competence, ability to work in a team, and very good communication and coordination skills, including interaction with stakeholders at all levels.
  • Openness and ability to actively contribute within a flat, agile organization.
  • Practical experience in implementing technical GMP requirements of regulatory authorities (Swissmedic, FDA, EMA) in investment projects and operations engineering
  • Focus on delivering results that make a valuable contribution to the business.
  • Quick comprehension skills as well as the ability to break down complex issues and communicate them in appropriate language to customers or authorities.
  • Autonomous and independent handling of complex tasks as well as reliable enforcement of agreed priorities.
  • Very good German and English language skills are required.

Sounds interesting? Apply now – we’re looking forward to receiving your applications!

Application Submission Deadline: 20.07.2026

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