Sr Quality Control Technician - Operations (12 months)
Key information
- Publication date:21 August 2025
- Workload:100%
- Place of work:Allschwil
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job Description
Position Overview: The Senior Quality Control Technician (m/f/d) ensures compliance with the highest quality standards in the pharmaceutical production environment. This position encompasses a variety of tasks related to the inspection, monitoring, and documentation of processes and materials, ensuring adherence to GMP standards.
Main Responsibilities:
- Start-Up Release: Preparation of room, machines, and materials before production start.
- In-Process Controls: Conducting regular in-process controls to ensure compliance with regulations.
- Final Inspections: Performing final inspections of packaged study medication (blind check).
- Quality Decisions: Making quality decisions in the respective work areas/cabinets.
- Prevention of Deviations: Implementing measures to avoid process deviations.
- Deviation Management: Initiating deviation reports in Global Trackwise.
- Microbiological Monitoring: Conducting microbiological measurements to ensure a sterile environment.
- Material Management: Managing quarantine and release of materials in the operation.
- Inspection Rounds: Conducting weekly inspection rounds in production areas.
- Machine Monitoring: Supporting and performing device monitoring and calibration.
- Documentation: Creating standard operating procedures (SOPs) and forms in the electronic document management system (eDMS).
- Environmental Monitoring: Reviewing weekly and monthly temperature and humidity measurements.
- Light Measurements: Conducting light measurements as needed.
- Support Requests: Handling and supporting internal and customer inquiries.
- Logbook Management: Checking and archiving logbooks.
- Reporting Issues: Informing direct supervisors about all encountered problems.
- Training Needs: Identifying personal training needs and supporting the training of new employees on the job.
Qualifications:
- Experience in pharmaceutical manufacturing and/or quality control.
- Knowledge of Good Manufacturing Practice (GMP).
- High level of accuracy and efficiency.
- Strong sense of responsibility and reliability.
- Ability to work in shifts (06:00-14:00, 14:00-22:00).
- Fluent German skills, English is an advantage.
- Experience with Microsoft Word and Excel.
Additional Information: This job description does not include all tasks and responsibilities required for this role. All additional duties, tasks, or responsibilities requested by the team leader or manager must be performed accordingly.
Have we sparked your interest? We look forward to hearing from you!
