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Johnson & Johnson

Cleaning Validation Engineer

Posted Mar 4, 2022
Job ID: JJJP00010326
Location
Leiden
Hours/week
40 hrs/week
Timeline
1 year
Starts: Mar 13, 2022
Ends: Mar 1, 2023
Payrate range
28 - 30 €/hr
Application Deadline: Mar 20, 2022 12:00 AM

Cleaning Validation Engineer

The Netherlands, 1-year contract, 36h-40h, Hybrid way of work 


 

Johnson & Johnson Worksense (via Randstad Sourceright) is responsible for finding, engaging, and contracting talent for the Johnson & Johnson contingent workforce.

 

We are currently recruiting a Cleaning Validation Engineer to join our contingent workforce on a growing team in Janssen Pharmaceuticals in Leiden for a 12-month contract. 

We are looking for someone who likes challenges, is collaborative, and is keen on working within project teams.

 

In this role, you will be a team member of Leiden site Technical Operations. 

Leiden site Technical Operations is part of the global Technical Operations organization that 

manages the technology platform strategy within Leiden as well as across the other parenteral sites. 


 

You as a Cleaning Validation Engineer will be responsible for:

  • Cleaning validation studies that are executed conform to site standards and Johnson & Johnson guidelines. 
  • Participate in multidisciplinary projects as an independent team member within Janssen Biologics.
  • Assessment of change controls, preparation of validation assessments, and performing PQA (performance qualification assessment).
  • Ensuring that all change control actions are determined and executed within agreed timelines.
  • Supporting in deviation investigations.
  • Contributing to standardization and improvement initiatives related to the project activities/processes/procedures.
  • Performing Process Qualification Assessments (PQA) and assessing the impact of the change on PQ of supporting processes (cleaning/mixing) for both new and established products


 

You as a  Cleaning Validation Engineer have:

  • Master’s degree in a relevant field (e.g., pharmaceutical sciences, biotechnology, biochemistry, life sciences, biological engineering, etc)
  • Min 3 years experience in a pharmaceutical environment. 
  • Min 1 year of experience with cleaning validation (of ex: PGCS, UFDF, columns, other equipment, etc) and change control assessment
  • Expertise in process excellence and/or project management is a plus;
  • Experience with Process Qualification Assessments
  • Flexible, independent, and proactive
  • Good command of English (spoken and written) is required



If you meet our requirements and are interested in hearing more about our Cleaning Validation Engineer role, please do not hesitate to apply through the provided link today and a member of our recruitment team will be in touch!


 

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