On behalf of our client, a growing company based in Neuchâtel, we are currently looking for a
Senior Analyst, Quality Control
Vos tâches
POSITION SUMMARY
The QC Analyst I is part of the Sample Management & Incoming testing Packaging team in the Quality Control
department at BMS Boudry.
This team is responsible for the management of all QC samples, visual testing of samples, incoming packaging materials
testing, preliminary investigations on samples associated with product complaints as well as support activities for the
QC department.
The main responsibilities of the position will be to ensure the follow-up of laboratory samples (raw material, incoming
packaging materials, stability samples) from receipt to destruction, performed and reviewed « visual control » laboratory
tests, and provide logistical support to the Analytical QC group (e.g., stock management and ordering of consumables
and laboratory equipment). QC Analyst I will also participate in projects relating to laboratory safety and continuous
improvement.
All activities will be performed in full compliance with laboratory procedures and safety rules (EHS) as well as Good
Documentation and Good Manufacturing Practices (GDP and GMP).
DUTIES/RESPONSIBILITIES
• Perform reception, testing, reconciliation, destruction, referencing of samples such as semi-finished products
incoming raw materials, primary and secondary packaging, stability, standard retention or special samples (…)
• Perform raw data review
• Execution of analyses such as primary and secondary packaging, AQL, visual inspection of pharmaceutical
products and of pharmaceutical products and referencing of semi-finished/finished products (…)
• Visual examination of stability, complaint and reference samples (…)
• Archiving
• Management of Laboratory material orders (« Kanban » system, creation of order supplier contact, follow-up,
reception, labeling and storage) (…)
• Execution of actions (CAPA, Deviation actions…) associated with Quality Systems (requested by QC
Management)
• Implementation of continuous improvement actions in the laboratory (requested by QC Management)
• Report immediately any incident/ EHS event (incident opening)
• Any other activities assigned by QC management
• Execute tasks as assigned
Votre profil
KNOWLEDGE, SKILLS, AND ABILITIES:
• CFC Laboratory Technician or equivalent combination of education training and experience
• Minimum 2 years of experience in a GMP/GDP environment or in a regulated industry
• Good knowledge of quality control operations in a GMP-regulated environment
• Expertise of laboratory safety rules, general organization and workflows of a quality control laboratory
• Basic knowledge of analytical techniques like IR, Spectro colorimeter, balance…
• Familiarity with standard oice tools (Windows Excel and MS Oice)
• Proficient in the use of a LIMS (Laboratory Information Management System)
• Strong collaboration and communication skills with QC team members and other departments
• Fluency in French and notions of English
• Knowledge of LEAN and 5S philosophy
Date d'entrée
À convenir