contrôle qualité

☞ Adecco

View: 151

Update day: 14-04-2024

Location: Boudry Neuchâtel NE

Category: Pharmaceutical / Chemical / Biotech IT - Hardware / Networking Information Technology

Industry:

Job type: CDD

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Job content

Pour notre client situé à Boudry, nous recherchons un/e controleur de qualité.

contrôle qualité

Votre défi

The QC Analyst Equipment Specialist is part of the Technical Support team of the Quality Control (QC).
The main responsibility of the position will be to perform super user activities for the laboratory
computerized systems, including Master Data Management activities, and associated GMP document
updates. The QC Analyst Equipment Specialist will act as a Super user providing support and training to End-Users of the QC laboratories as well as supporting investigations and resolution of issues.
The QC Analyst Equipment Specialist will also support activities related to acquisition and qualification of new equipment, investigation and troubleshooting of analytical and equipment issues as well as introduction of new products to the QC laboratories.
All activities are carried out in compliance with laboratory procedures and safety rules (EHS) as well as good documentation and manufacturing practices.


Vos compétences

  • CFC as Laboratory Technician or BS degree in Science, Chemistry, or equivalent.
  • A minimum of 2 years of relevant work experience in a GMP regulated environment (or equivalent). Previous experience of laboratory equipment qualification is a plus.
  • Advanced knowledge and interpretation of cGMP, ISO, FDA, MHRA and Pharmacopeia requirements, and good documentation practices.
  • Good knowledge of Data Integrity principles, familiar with audit trail review requirements.
  • General computer literacy including MS Office (Word, Excel, PowerPoint, Outlook, Visio)
  • Good knowledge of basic coding and code reviews.
  • Good knowledge of LIMS, Oracle and Empower applications.
  • Good scientific knowledge and hands-on experience of chromatography techniques (HPLC, UPLC, GC), dissolution, UV/VIS, potentiometry and IR techniques.
  • Effective verbal communication skills, ability to interact with different levels of the organization: supervisor, peers, lab analysts, and other departments
  • Effective technical writing skills, experience writing GMP documents (procedures, protocols, plans and reports) as well as deviations and investigations.
  • Professional command of French and English, verbal and written.
  • Proven time management skills and a strong attention to detail.
  • Proven analytical and problem-solving skills.
  • Ability to work independently and compliantly.


Vos perspectives

CDD 6 months


Votre contact

Monsieur Raphael Bader, Consultant Retail, répond à toutes vos questions au Tel. +41 58 233 3000.

Vous pouvez postuler directement en ligne.

Merci de préciser la référence 023-RBAD-165800-70-FR.
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Deadline: 29-05-2024

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