Process Technician – Supply Management (7090)

About Us

CTC is a specialized search and recruitment partner for the Life Sciences industry, with over 25 years of experience in connecting talented professionals with meaningful career opportunities. We collaborate with our clients to engage, retain, and develop the right talent as needed.

Our Client

Our client is a prominent global player in the Pharmaceutical industry, headquartered in Basel, Switzerland. The organization is currently undergoing a cultural transformation and enhancing its external perception. They are focused on developing novel therapies in Oncology and Ophthalmology, while also advancing a world-leading pipeline in Neuroscience and Dermatology, recognized for having one of the strongest pipelines of Phase II/III studies globally.

Role Responsibilities

As part of your role, you will be executing assigned manufacturing tasks in the hand packaging of clinical trial samples according to the production plan, ensuring timely product delivery with adherence to quality standards and relevant GMP, safety, and environmental guidelines. Key responsibilities will include:

• Manual labeling and packaging of primary packaged medications for clinical trials.
• Executing all assigned tasks according to the production schedule and applicable GMP, operational, environmental, and safety guidelines.
• Timely and accurate completion of batch documentation as part of the production process.
• Contributing to the operational management of the production area (workplace cleanliness, orderliness, 5S, etc.).
• Adhering to health, safety, and environmental regulations (HSE).
• Applying current GMP regulations in all activities.
• Conducting process-related controls and maintaining correct documentation of all tasks, both in paper form and electronically, in accordance with GMP requirements.
• Embracing continuous improvement and analyzing weaknesses, suggesting improvement measures regarding organization, processes, safety, hygiene, etc.
• Participating in all relevant functional training and maintaining the necessary training standards.
• Managing or participating in projects aimed at continuous improvement aligned with strategic goals.
• Collaborating with other units and being willing to work in other areas when needed (e.g., primary packaging, warehouse, label printing).

Qualifications

• Relevant working/residency permit or Swiss/EU Citizenship required.
• Experience in the GMP area and the packaging of pharmaceutical products.
• A self-reliant, communicative, and flexible personality with a precise and reliable working style, even under time pressure.
• A true team player with a strong sense of teamwork.
• High responsibility and diligence in documentation, organization, and cleanliness at the workplace.
• Constructive approach to work, flexibility, solution-oriented mindset, and accountability for one’s own work with a deep understanding of quality.
• Strong self-motivation and a quick learner, able to adapt to new tasks promptly.
• Fine motor skills and enjoyment in performing tasks with precision.
• Proficiency in standard PC programs (MS Office); knowledge of SAP is advantageous.
• Good knowledge/experience in GMP environments or hygiene-critical areas.
• Excellent command of the German language, spoken and written; knowledge of English is advantageous.

We invite you to explore the opportunities that await you and learn more about our initiatives and how we can collaborate to achieve success in the pharmaceutical industry.