QC Equipment Qualification Engineer

Randstad (Schweiz) AG

Randstad (Schweiz) AG

Postuler

Infos sur l'emploi

  • Date de publication :

    08 mai 2024
  • Taux d'activité :

    100%
  • Type de contrat :

    Temporaire
  • Langue :

    anglais (Courant)
  • Lieu de travail :

    Bern
Jobdescription

For our client, an international company based in Bern, we are seeking a highly skilled Equipment Qualification Engineer for a 6-month contract position to support capital expenditure (CAPEX) projects.

As an Equipment Qualification Engineer, you will play a crucial role in ensuring the successful qualification of Quality Control (QC) equipment in compliance with applicable regulations and industry standards.

 

 

General Information:

 

  • Start date: ASAP
  • End date: min. 6 months
  • Extension: possible, to be discussed
  • Workplace: Bern
  • Workload: 100%

 

 

Key Responsibilities:
 

 

  • Support the overall equipment qualification activities focusing on QC equipment.
  • Collaborate with project stakeholders to develop qualification plans, protocols, and reports for QC equipment.
  • Execute qualification activities, including installation and operational qualifications (IQ/OQ) for QC equipment.
  • Conduct system turnover verification, functional testing, and documentation of results for QC equipment.
  • Work closely with cross-functional teams to coordinate and integrate equipment qualification activities within project timelines.
  • Identify and mitigate risks during the qualification phase, ensuring compliance with regulatory requirements and safety standards.
  • Utilize industry best practices and standard operating procedures to conduct equipment qualification activities.
  • Collaborate with project team members to ensure accurate and timely completion of documentation for equipment qualification.
 

Your Profile:
 

  • Bachelor's or Master's degree in Engineering or a related field.
  • Minimum of 5 years of experience in commissioning and qualification activities in in pharmaceuticals or biotechnology industry.
  • Strong knowledge and understanding of GMP (Good Manufacturing Practice) guidelines and regulatory requirements.
  • Experience in developing and executing commissioning and qualification plans, protocols, and methodologies.
  • Proficient in conducting system turnover verification, functional testing, and documentation of results.
  • Familiarity with qualification activities such as IQ/OQ.
  • Excellent problem-solving and analytical skills, with the ability to identify and resolve issues proactively.
  • Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
  • Detail-oriented, with exceptional organizational skills and the ability to manage multiple tasks and priorities simultaneously.
  • Availability to commit to a minimum of 6-month contract duration.
  • Business fluency in English, German language is a plus
Luca Furler

Contact

  • Randstad (Schweiz) AG

Postuler