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  • project engineer qualification

Project Engineer Qualification

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  • Basel, Basel-City
  • posted today

Job details

Summary

  • Basel, Basel-City
  • Temporary
Posted 17. november 2025
  • Reference number
    24187
    W

    Walentyna Dobrowolska

    • +41 58 201 56 71

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randstad professional

randstad professional

We bring diverse and pre qualified professional talent and businesses together to connect the right people with the right roles. By building specialized teams, we help individuals flourish in their careers and businesses succeed.

Job details

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

...

General Information:

  • Start date: asap
  • Latest possible start date: 01.12.2025
  • Duration: permanent
  • Workplace: Basel
  • Workload: 80-100%
  • Remote/Home Office: possible, max 1 day per week
  • Travel: only when necessary for projects
  • Working hours: Standard
  • Team: 18 people
  • Department: Pharma Engineering DP


About the job:

Pharma Engineering is looking for suitable candidates with experience in plant qualification in the area of Pharma Engineering Solida.

The work environment includes process plants, media, energy, room air conditioning such as reactors, fermenters, centrifuges, pure water, steam, autoclaves, clean rooms as well as small parts washing machines.


Your Profile:

  • GMP experience
  • Understanding of the implementation of qualifications in the pharmaceutical environment.
  • Great communication skills


Tasks & Responsibilities:

  • Creating qualification plans/reports for the DQ-IQ-OQ-PQ phases according to the Quality System.
  • Conducting qualifications in the DQ-IQ-OQ-PQ phases according to the Quality System.
  • Creating QPPs/MQPs (Qualification Project Plans/Master Qualification Plans).
  • Evaluating technical changes to systems with regard to their impact on the qualified status and independently processing requalifications.
  • GMP-compliant documentation of the work performed and summarizing any differences that arise.
  • Developing suggested solutions for any differences that arise.
  • Familiarization with electronic qualification and validation software.


Must Haves:

  • Degree in a natural sciences/engineering program or relevant professional experience
  • Min. 3 years of professional experience and solid experience in the qualification process
  • Several years of experience in the GMP area with in-depth understanding of quality systems and the lean implementation of GMP requirements
  • Good MS Office skills
  • Very good written and spoken German, good English skills


Sounds interesting? Apply Now! We look forward to receiving your application.

Application Submission Deadline: 30.10.2025

Show more

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


General Information:

  • Start date: asap
  • Latest possible start date: 01.12.2025
  • Duration: permanent
  • Workplace: Basel
  • Workload: 80-100%
  • Remote/Home Office: possible, max 1 day per week
  • Travel: only when necessary for projects
  • Working hours: Standard
  • Team: 18 people
  • Department: Pharma Engineering DP


About the job:

Pharma Engineering is looking for suitable candidates with experience in plant qualification in the area of Pharma Engineering Solida.

The work environment includes process plants, media, energy, room air conditioning such as reactors, fermenters, centrifuges, pure water, steam, autoclaves, clean rooms as well as small parts washing machines.


Your Profile:

  • GMP experience
  • Understanding of the implementation of qualifications in the pharmaceutical environment.
  • Great communication skills

...

Tasks & Responsibilities:

  • Creating qualification plans/reports for the DQ-IQ-OQ-PQ phases according to the Quality System.
  • Conducting qualifications in the DQ-IQ-OQ-PQ phases according to the Quality System.
  • Creating QPPs/MQPs (Qualification Project Plans/Master Qualification Plans).
  • Evaluating technical changes to systems with regard to their impact on the qualified status and independently processing requalifications.
  • GMP-compliant documentation of the work performed and summarizing any differences that arise.
  • Developing suggested solutions for any differences that arise.
  • Familiarization with electronic qualification and validation software.


Must Haves:

  • Degree in a natural sciences/engineering program or relevant professional experience
  • Min. 3 years of professional experience and solid experience in the qualification process
  • Several years of experience in the GMP area with in-depth understanding of quality systems and the lean implementation of GMP requirements
  • Good MS Office skills
  • Very good written and spoken German, good English skills


Sounds interesting? Apply Now! We look forward to receiving your application.

Application Submission Deadline: 30.10.2025

Show more