QRM Data Verification Assistant (m/f/d)

QRM Data Verification Assistant (m/f/d) – data verification / data handling / GMP / database handling / german

Project:
For our customer a big pharmaceutical company based in Kaiseraugst we are looking for a highly qualified QRM Data Verification Assistant (m/f/d)

Background:

Quality Risk Management records are migrated from a legacy system to a new system. The migration is quite challenging and requires a 100% manual check of the migrated data including potential correction, also known as data verification. Further the risk records need to be updated according to the project plan to reflect the current situation. Aim of this position is to perform the verification and correction of the migrated risk records in the new system in collaboration with quality management and other functions as required and to perform updates of the risk records.All tasks are conducted with close contact to Quality Assurance, QRM Owner and other stakeholders.

The perfect candidate:
The perfect candidate has experience in a GMP regulated environment and in the pharmaceutical industry. The perfect candidate has first experience in data verification or data handling and a sound knowledge of risk management. She/he has a rapid grasp regarding new IT systems and has a firm understanding which impact GMP documentation makes. She or he proceeds the required approvals with a sound knowledge of regulatory requirements as well as internal Pharma Quality Standards (PQS) and ensures compliance of these.

Tasks & Responsibilities:

• Data Verification between legacy system and new One QMS (Veeva QRM)
  * Close communication with risk record owner, SMEs and other stakeholders
  * Approval of verified and/or updated risk records
  * Ensure compliance of approved records with internal and external standards and specification
  * Owner role for unplanned events

Must Haves:

• Completed apprenticeship e.g. as lab technician, chemical technician or comparable background
  * Min. first Experience in data verification or data handling
  * Min. 3 years experience in a GMP regulated, pharmaceutical industry e.g. during apprenticeship
  * Experience in Risk Management
  * Common office software (e.g. Google, Microsoft), good understanding of Excel/GSheet, database handling
  * Language skills: German (fluent), English (min. B2)
  * Accurate and solution-oriented working, teamplayer

Reference Nr.: 922618TP
Role: QRM Data Verification Assistant (m/f/d)
Industrie: Pharma
Workplace: Kaiseraugst
Pensum: 80-100%
Start: 01.07.23
Duration: 8++
Deadline: 11.05.23

If you are interested in this position, please send us your complete dossier via the link in this advertisement. If this position does not fit your profile and you wish to be considered for another position directly, you can also send us your dossier via this ad or to jobs[at]itcag[dot]com.

Contact us for more information about our company, our positions or our attractive Payroll-Only programme: +41 41 760 77 01.

About us:

ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering.

We offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.