Process Technician - Materials Management, GMP

Project overview

Process Technician - Position in the area of Materials Management, GMP, to be filled at our client in the pharmaceutical industry in Basel.

Execution of assigned manufacturing tasks in the hand packaging of clinical trial materials according to the production plan, to enable timely production of the product in quality and quantity according to relevant GMP, safety, and environmental guidelines.

Responsibilities

• Manual labeling and packaging of primary packaged medicines for clinical trials
• Execution of all assigned activities according to the production plan and valid GMP, work, operational, environmental, and safety instructions and guidelines
• Timely and error-free creation of batch documentation (part of production)
• Participation in the housekeeping of the production area (workplace cleaning, order, 5S, etc.)
• Compliance with health, safety, and environmental rules and guidelines (HSE)
• Application of current GMP rules
• Execution of process-related controls
• Correct and accurate documentation of performed activities on paper and in electronic batch documentation, according to GMP regulations
• Readiness for continuous improvement and analysis of weaknesses, proposing improvement measures (organization, process, safety, hygiene, etc.) at the production site
• Participation in all function-relevant training courses and maintenance of a required training level
• If necessary and applicable, readiness for overtime or shift work (early and late shift).
• Proposing improvement measures (organization, process, safety, hygiene, etc.) at the production site
• Management/participation in continuous improvement projects according to strategic goals
• Collaboration with other units and readiness for assignments in other areas if needed. (e.g., primary packaging on equipment, warehouse, label printing)

Requirements

• Experience in the GMP area and in the packaging of pharmaceutical products
• You possess an independent, communicative, and flexible personality and have an exact and reliable way of working, even under time pressure
• Team player with good team spirit
• High sense of duty and diligence (documentation, order, and cleanliness at the workplace)
• Constructive working method, flexibility, solution-oriented, responsibility for one's own work, deep understanding of quality
• High self-motivation and quick comprehension to learn new activities
• Fine motor skills, enjoyment of precise work
• Confident use of standard PC programs (MS-Office), knowledge of SAP is an advantage
• Good knowledge/experience in the GMP environment and/or hygiene-critical areas
• Very good language skills in German (spoken and written), English skills are an advantage

Project details

Basel, Switzerland

Work Model: On-site

Sector: Pharma

01/10/2026

12+ months

100%

Ref. No.: BH 24600

Take the next step and send us your CV as well as a phone number where we can reach you during the day.

Due to Swiss labor law, we can only consider applications from Swiss citizens, EU citizens, and individuals with a valid work permit for Switzerland.

We welcome applications from people of all genders, ages within the working age range, sexual orientations, personal expressions, ethnic origins, and religious beliefs. Therefore, information about gender or a photo is not required in your application.

Due to client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore possible solutions together with our end client.

• Start: flexible
• Location: Basel, Basel-Stadt, Switzerland, CH
• Rate: 32-36 EUR/h
• Languages: German