Senior Scientist Monitoring

Posted 8 hours 48 minutes ago by Gi Life Sciences Switzerland

Permanent
Not Specified
Laboratory Jobs
Not Specified, Switzerland
Job Description

Key Responsibilities :

As such, this position's scope of responsibilities are to:

  • Establish and maintain quality systems associated with monitoring of utilities and environment.
  • Act as contact in case of a project related to monitoring.
  • Develop and maintain procedures, working instructions, protocols/report templates related to Environmental Monitoring and Clean Utilities qualifications.
  • Drive the creation of Risk Assessments for definition of qualification and routine monitoring sampling points for CU and EM.
  • Support CVQ team for protocols and reports establishment.
  • Develop the monitoring and trending program including required procedure and monitoring/trending reports.
  • Work collaboratively with all stakeholders to ensure that monitoring activities are planned and executed efficiently.
  • Support the implementation of Laboratory Instrument Management System (LIMS)and other IT tool required for qualification and routine Monitoring.
  • Support deviation resolution related to monitoring in cooperation with key partners (PRO, QMO, QCS).
  • Ensure regulatory inspections by presenting qualification procedures, strategies and all related monitoring documents.
  • Adheres to general cGMP rules, Quality policies, procedures and instruction as rolled out by the Quality function and endorsed by the site management.
  • Actively contributes to continuous quality improvement initiatives and deviation reporting and follow-up.
  • Adheres to general safety rules, policies, procedures and instructions as rolled out by the EHSS functions and endorsed by the site management.
  • Actively contributes to safety initiatives and issues as well as near miss reporting and follow-up.

Profile

  • University degree in (Bachelor or Masters) in Life Sciences (Biology, Chemistry, etc.), Dipl. Ing. or . or . or equivalent.
  • Language: Fluent in English, Fluency in German is a plus.
  • Experience in the bio-pharmaceutical industry.
  • Knowledge of cGMP including current knowledge of industry guidance documents and standards focusing on facility monitoring (Engineering and microbiology).
  • Experience in Quality Systems like Change control, deviation including investigation, CAPA implementation.
  • Intellectually curious and embraces Practical Process Improvement (PPI).

For further details or inquiries feel free to get in touch through email.

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