Life Science Consultant, Research and Science Lab Quality Associate

☞ Kvalito Consulting Group

Visualizza: 146

Giorno di aggiornamento: 25-04-2024

Località: Basel Basel-Stadt BS

Categoria: R & D IT - Software

Industria: Pharmaceutical Manufacturing

Posizione: Associate

Tipo di lavoro: Full-time

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Contenuto del lavoro

We are looking for enthusiastsKVALITO Consulting Group is a strategic partner and global Life Science network for regulated industries with a focus on quality. Headquartered in Basel, Switzerland, we have subsidiaries in Germany, Czech Republic, Ireland and Malaysia. With our enthusiasm for progressive technologies and our in-depth knowledge of industry best practices and regulations, we drive effective and efficient project delivery to keep our industry-leading clients ahead of the competition. Our leadership and consultants combine decades of experience in enterprise environments. To cover all essential technical areas in the field of digital and mobile, KVALITO works with reliable Technology Partners worldwide. For more information, please visit us at www.KVALITO.ch.Life Science Consultant, Research and Science Lab Quality AssociateRole PurposeThe associate in Research Quality & Compliance is responsible for managing quality programs applicable to the wide range of discovery science and research activities conducted by our client globally. The candidate will partner with internal and external groups to support the implementation and improve relevant practices, facilitate Quality issue resolution and provide appropriate Quality support to meet business and health authority expectations while maintaining the highest scientific standards and promoting a culture of quality and compliance.Major Accountabilities
  • Provide training for review of project documentation and data integrity principles.
  • Interact with external parties and obtain buy-in from key internal and external stakeholders
  • Interacts with our client internal groups on the integration program
  • Provide guidance and be involved in submission readiness & Quality oversight for non-GLP studies
  • Execute reviews of project documentation (e.g. Lab notebooks and systems) using semi-automated process and submission to our client and disease area management.
  • Ensure group SharePoint / MS Teams site is up to date and provide content.
  • Raise the legacy data integrity training material to the next level to further engage with our client’s business.
  • Provide expertise on internal regulation on the use of HT.
  • Attend our client’s Quality team meetings
  • Conduct interviews for our client’s internal and external assessments
Minimum Qualifications And ExperienceEducation
  • Master of Science in a biology-related field (molecular biology, microbiology, Biochemistry) and experience in quality and/or related experience preferred.
Language
  • Fluent in English written & spoken
  • Additional language skills in German, French are highly appreciated
Work Experience
  • Demonstrated experience in a quality fuction and dealing with data integrity topics in research areas
We Offer Great Benefits
  • Flat hierarchies and responsibility from the beginning
  • People-oriented culture
  • Diversity and inclusion focused environment
  • Global client projects in a multinational environment
  • Flexible working hours and home-office
  • Involvement in global conferences
  • Individual professional development, training, and coaching
  • Unlimited full employment contract
  • Excellent remuneration package consisting of a competitive salary plus a substantial bonus
ContactIf you have the necessary background and experience and would like to join a small team responsible for a truly global operation, then please send your application to recruiting(at)kvalito.ch including your:
  • CV, cover letter and supporting documents (i.e., diplomas, certificates, references)
  • Availability - earliest start date
  • Salary expectations
  • Location preference
We are looking forward to your application.Your KVALITO Team.
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Scadenza: 09-06-2024

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