Clinical Labeling and Packaging | Operator | GMP | SAP | MES | Manual | Packaging
Your new role As an Operator in the Clinical Labeling and Packaging department at Amgen Breda, you will be responsible for carrying out labeling, packaging, and assembly activities for clinical trials conducted globally. You will work with a small, high-performing team (5-6 operators) in the day shift (08:00-16:30) to ensure that every patient receives a clinical drug of high quality. Your tasks include: Executing labeling and packaging processes according to standard operating procedures (GMP). Taking responsibility for documentation in the Electronic Batch Record (EBR) and ensuring all tasks are properly recorded. Supporting the warehouse team during busy periods by performing warehouse activities. Ensuring that training requirements and deadlines are met. Executing batch-related logistical processes.
Your profile We are looking for someone who can thrive in a dynamic and changing work environment. You are eager to learn, reflect on your work, and constantly seek ways to improve. Additionally, you will identify with the following profile:A minimum of 2 years of experience in a (manual) packaging environment, preferably in the pharmaceutical sector (GMP/GDP environment). Focused on quality, efficiency, and performance improvement in work processes. Willing to work in a complex, manual packaging environment and sometimes under cold conditions (2-8 °C). Comfortable working in an international and multicultural environment. Experience with SAP/MES is a plus.A mindset of continuous improvement with respect to your role, and a team player attitude. Your organisation Amgen Breda is responsible for executing labeling, packaging, and assembly activities for clinical trials conducted globally. The Clinical Labeling and Packaging department plays a crucial role in delivering clinical drugs of the highest quality. The team consists of dedicated professionals who collaborate in a dynamic, hands-on environment where accuracy, teamwork, and flexibility are key. You will have the opportunity to work in an innovative, international organisation focused on delivering high-quality products for clinical trials. We offer a dynamic work environment with room for personal development and growth. Additionally, you can expect: A challenging role with significant responsibility and room for initiative.Training and development opportunities to further enhance your skills and knowledge.A competitive salary and comprehensive secondary benefits.
Click hereto access HAYS Privacy Policy, which provides detailed information on how we use and protect your personal information, and your rights in relation to this.
Summary
Job type
Temporary
Industry
Engineering
Location
Breda
Specialism
Engineering
Pay
3350 including 13th bonus
Ref:
1048704
Closing date
24 Jul 2025
Talk to a consultant
Talk to Jelmer van Doorn, the specialist consultant managing this position, located in Tilburg