Position: Mid-Senior level

Job type: Full-time

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Job content

Responsibilities

  • Development, implementation and execution of URS, SIA, DQ, IQ, OQ, PQ, RV and TM activities for mainly small scale equipment. Develops, implements and executes validation studies for cGMP-critical process systems to demonstrate compliance to cGMP-, User- and Regulatory requirements. Hands-on activity envisaged in relation to this.
  • Performs validation of systems in scope for which there is industry precedence but standards require interpretation to the particular case and in accordance with cGMP’s
  • Ensures that the Validated Status of systems in scope is in compliance with cGMP at all times.
  • Keeps current on emerging validation regulations and validation testing practices in order to meet or exceed cGMP requirements. Provides technical assistance on current US FDA and EU validation requirements.
  • Generates validation documentation (protocols/reports) and provides assistance with the execution of protocols for systems in scope.
  • Responsible for the validation documentation through approval and implementation.
  • Provides input in review/assessment of changes to as whether they impact the validated status and validation-documentation, as appropriate.

Requirements

  • Knowledge of CGMP requirements in a regulated environment.
  • Understanding of relevant quality and compliance regulations.
  • Capable of troubleshooting validation issues.
  • Good knowledge of quality management systems
  • Experience: 2-4 years experience working in a Healthcare manufacturing environment, with experience in qualification of small scale equipment (including the related software).

Terms

  • Challenging projects based on your interests and skills
  • Personal follow-up and clear, transparent communication both before and after commencement of employment
  • Possibility to follow extra training
  • Inspiring network events and legendary after work drinks
  • Strong network of industry leading clients
  • Expertise within IT, Engineering and Life Sciences
  • A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employees
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Deadline: 31-12-2025

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