Aktualnie prowadzone rekrutacje

With offices in Berlin, Warsaw and Prague, KCR Placement is an international boutique provider of ‘fit for purpose’ resourcing solutions for a wide array of functions, including expert, managerial and senior executive ones. We specialize in finding the right talents for Pharmaceutical, Biotech, Medical Device companies and Contract Research Organizations across Europe. 


We're onboarding best-in-class candidates, so give us a chance to meet you!

Current Vacancy Highlights:

QUALITY ASSURANCE ASSOCIATE / GERMANY

KCR Placement is a trustworthy provider of “fit for purpose” resourcing solutions for pharmaceutical and biotechnology companies in Europe. For our Client we are currently looking for experienced candidates for the position of Quality Assurance Associate

 


Quality Assurance Associate
 

 

Location: Berlin, Germany
Type of Contract: Permanent, office-based
Seniority: Associate

 

Duties associated with the role:

  • Support in ensuring company compliance (documentation and process compliance) with applicable regulations, SOPs, good practice standards,
  • Being up-to-date with regards to GXP (GCP, GMP, GDP) regulations/guidelines – maintenance of quality knowledge database,
  • Support in SOP writing and improvements (cooperation with other departments to increase the quality and consistency of KCR SOPs) - verification of SOP framework in order to identify and correct process gaps, discrepancies, inconsistencies in cooperation with applicable Functional Area Leads and Quality Assurance Team, 
  • Provide support in maintenance and further development of KCR SOP and CAPA systems (support in improving quality tools, trackers and metrics), keeping quality tools and trackers up to date, preparing of quality status reports, 
  • Providing support to Quality Assurance Auditors in audit preparation and follow-up activities  (audit scheduling, collection and filing of audit documentation, audit follow-up communication), 
  • Reporting to Quality Assurance Manager


Desired Skills and Experience:

  • Experience in a clinical research environment with strong working knowledge of ICH-GCP regulations
  • 1-2 years of engagement in quality assurance activities (CRO or Pharma GxP exposure)
  • Fluent command of English
  • Very good work management, ability to set priorities
  • Proactivity and self-motivation
  • Attention to details when working on different projects


 

We’re onboarding “best in class” candidates, so give us a chance to meet you!
 
NOTE: When applying please kindly enclose the following statement:

"I hereby give my consent to the processing of my personal data included in the CV provided by me (within the scope beyond the contractual authorization), by KCR Placement Sp z o.o. on behalf of its clients with its seat in Warsaw (6 Postepu str, 02-676 Warsaw) as the data administrator, for the purposes related to the recruitment process conducted by the said entity. This consent also includes the processing of my personal data within the above scope in any future recruitment processes, unless the aim of such processing changes."
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