Qualification and Validation Engineer (m/f/d) at xing
berlin, Berlin, Germany -
Full Time


Start Date

Immediate

Expiry Date

24 Nov, 26

Salary

0.0

Posted On

26 Aug, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Pharmaceutical Manufacturing

Description

About this job

Do you want to not only support projects in the pharmaceutical and medical technology sectors, but truly drive them forward on-site – with a sound technical foundation, GMP compliance, and as an equal within the team? Then you can expect a role with substance, responsibility, and a clear development perspective from us.

We are a specialized consulting and project management company for the pharmaceutical, medical technology, and other regulated industries. We implement projects for renowned clients – with a focus on quality, reliability, and collaborative teamwork.

As a qualification and validation engineer, you work closely with the customer on site, plan and document qualification activities and ensure that systems and processes are commissioned and operated in a traceable, compliant and safe manner.

Your tasks:

  • Conducting GMP risk analyses
  • Planning and implementation of training programs: - Design Qualification (DQ)
  • Installation Qualification (IQ)
  • Operational Qualification (OQ)
  • Performance Qualification (PQ)
  • Summary of results in qualification reports
  • Participation in process validations and/or cleaning validations
  • Working according to internal and external quality standards
  • Contributing to high customer satisfaction through clear communication, reliability, and quality of results.

What makes this role attractive:

  • Projects with substance in a GMP-regulated environment (pharmaceuticals/medical technology)
  • Steep learning curve: You quickly gain experience in various on-site projects.
  • Practical work at the interface between technology, quality and operations
  • Development perspective: You will build up professional foundations, tools and skills – as preparation for the next step towards project management or a senior role.

What you bring:

  • Completed studies in engineering or natural sciences, ideally with a focus on pharmaceutical or medical technology
  • Prior experience in plant qualification and/or process validation is a plus (but not a requirement).
  • Fluent English
  • You are willing to travel and work on-site on a project basis.

Your advantages with us:

  • Steep learning curve: You will quickly gain experience in various projects within the life science industry.
  • Mobility & Freedom: Company car for private use plus company bike
  • Flexible working & work-life balance: flexible working models and support in reconciling family and career
  • Strong sense of community: Team spirit fostered through company celebrations and regular team events.
  • More security & time for yourself: company-sponsored supplementary health insurance and sabbatical option
  • Does our culture suit you? Then apply now – we look forward to getting to know you. Send your application by email to: bewerbung@behrens-pm.de.

How To Apply:

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Responsibilities
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