Our Vacancy

Pharmaceutical process engineer H/F

  • Life Sciences
  • Permanent
  • Basel
  • 24/11/2021
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About Assystem

For 50 years, we've been driven by the firm belief that engineers are the architects of tomorrow's world, leading the way with their daring, their expertise and their ability to push boundaries.
Together with our customers, our 7,000 employees innovate on a daily basis and contribute to accelerating energy transition throughout the world. They support the world's greatest engineering projects in the fields of energy, healthcare, life sciences and transport.
A fast-growing international Group, we are present in 15 countries (in Europe, the Middle East, Asia and Africa).

Well known for our expertise in CQV (Commissioning Qualification Validation) and specialists in projects with strict technical and regulatory constraints, we partner pharmaceutical laboratories and high-tech industrial players to manage their capital expenditure and meet the challenges they face in terms of increasing safety and reducing costs and market lead times.
We innovate for our clients and provide them with disruptive technologies in the areas of data integrity, cybersecurity and predictive maintenance.

Assystem CARE combines 30 years of expertise in health and life sciences: the strength of engineering, the power of digital and experience in managing complex projects allow us to operate in highly regulated environments. We are a reference partner, agile and reliable in ensuring the success of projects in the health and life sciences industries.

Job Description

As a consultant, you participate to pharmaceutical projects and to the development of Assystem Care. You bring high value added technical solutions in the different project phase always in conformity with regulatory/quality requirements.  

Your mission includes :

  • Understanding the manufacturing process and production requirements (suers or/and quality requirements)
  • Participation to the definition of critical qualoty attributes and critical process parameters (CPP/CQA)
  • Daily management of deviation including investigation and root cause analysis.
  • Management of validation projects (product and/or cleaning) and improvement projects.
  • Participation to the definition of validation strategy and to the redaction of validation documents. Support of the tests execution.

Profile

With education training in chemical engineering, biology engineering or process engineering, you have relevant experience of 5 years minium in the pharmaceutical industry.


You have releavant experience in pharmaceutical or biopharmaceutical process. You have good knowledge of validation methodology.

Autonomous, rigorous, organized, you like technical work on the field as well as redactional work.

You speak fluently English and have intermediate level in German or French. 

At Assystem, everyone holds the reins for their own careers. Our role is to offer you the opportunities and resources you need to reach your full potential.

So why not join us and help shape the engineering landscape of the future?

 

We are committed to providing equal opportunities for every candidate and we celebrate all forms of diversity. At Assystem, only your skills matter!

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