Quality Control Analyst
vor 2 Wochen
Position: Analyste QC (en travail posté)
Company: Société internationale basée à Neuchâtel
Contract Duration: 24 months
Starting Date: As soon as possible
Contract: Through Randstad with possible extension
Location: Neuchâtel
Workload: 100%
Shift Information:
- Variable schedules: no fixed hours, can start between 6 am and 9 am, lunch break of 30 minutes to 1 hour between 11 am and 2 pm, and can finish between 4 pm and 8 pm. Flexibility is key. 40 hours worked from Monday to Friday within these time slots + additional weekend work at 25% and/or 50% extra pay on Saturday and Sunday. 4 days off (not necessarily consecutive) within a 14-day work period. This weekend work is separate from the regular schedule. Meals are not provided.
- On-call duty: 1 week per month. On-call personnel must be available by phone and ready to work during weekends or outside lab hours, paid 25 CHF per day during the week, 100 CHF on Saturdays and 100 CHF on Sundays. Mileage expenses are reimbursed only during on-call duties (for necessary travels).
Main Responsibilities:
- Sample control, aliquoting, identification, registration, distribution, storage, or disposal in compliance with current operational procedures and Good Manufacturing Practices.
- Adherence to good practices for sample reception, processing, and distribution as defined in procedures/protocols.
- Recording, documenting, and communicating any observed deviations during sample reception to relevant departments.
- Receiving and completing specific attributes for each sample in the appropriate system (if applicable) within defined deadlines.
- Receiving and recording backup samples in the relevant system.
- Recording backup sample transfers in the appropriate listed equipment.
- Performing backup sample withdrawals as requested by laboratories via the correct system.
- Executing backup sample destructions through the proper system.
- Sending samples to external sites or regulatory authorities according to defined schedules and procedures.
- Preparing cryotubes for production area sampling when required.
- Participating in validation protocol executions and stability studies where you are responsible for samples from receipt to analysis availability, or for stability or destruction when needed.
- Managing consumables and reagents stock levels in laboratories by ensuring timely ordering and replenishment.
- Performing regular equipment maintenance, calibration, temperature alarm checks following current procedures, and ensuring accurate completion of log-books and their review.
- Supporting QC teams in non-testing tasks (preparation of solutions for analysis, freezer transfers, autoclaving activities, etc.).
- Each team member must adhere to and enforce EHS rules. In case of deviations by colleagues or external parties, active reminder of EHS rule compliance is required.
- SME for a specific program or activity (may also present and defend topics during audits, gemba-walks, etc.)
Required Profile:
- Minimum Education Level: CFC in laboratory/biology or another relevant scientific field.
- Minimum 3 years of experience in a quality control laboratory within a cGMP environment.
- Desirable experience in electrophoresis analysis, Elisa, or enzymatic activity determination.
- Proficiency in technical French and English.
- Swiss or European nationality, or valid Swiss work permit.
- Willingness to work in shifts.
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