About the job
Join our Quality Control team at AbbVie, where you will be instrumental in ensuring the quality of raw materials used in our production processes. Under the guidance of the Microbiology and Raw Materials QC Manager, you will perform sampling and analysis in a highly regulated environment adhering to GMP (Good Manufacturing Practices) standards.
Key Responsibilities:
1. Sampling of Raw Materials
- Prepare sampling campaigns and conduct sampling of raw materials and gases.
- Ensure the supply of consumables for the sampling area.
- Contribute to maintaining the overall cleanliness and organization of the sampling area.
- Assist in tracking materials internally or with subcontractors, including verifying Certificates of Analysis (CoA).
- Coordinate with the logistics team for the preparation and shipment of raw materials for analytical subcontracting.
2. Participation in Material Release
- Carry out the release of consumables in SAP according to established procedures.
- Support activities related to sample management, including sample identification verification and periodic inventory participation.
- Open deviations (exception reports) related to material release activities.
- Notify Quality Assurance and/or management of any blocking issues or non-compliance.
3. Conduct QC Analyses on Raw Materials
- Perform identification analyses for specific raw materials.
- Verify laboratory data (logbook and double-check raw data).
- Ensure analyses are performed on qualified and calibrated equipment.
- Draft standard operating procedures, user manuals, and analytical protocols.
- Contribute to maintaining the overall appearance of the laboratory.
4. Monitoring, Documentation, and Quality
- Maintain rigorous traceability in analytical documents and quality systems.
- Open non-compliance events in the dedicated software and participate in laboratory investigations related to performed analyses.
5. Work Schedule and Organization
- Work in rotating shifts: morning and afternoon.
