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- Aufgaben: Assist scientists with routine analytical testing and sample handling in a GMP-regulated lab.
- Arbeitgeber: Join Coriolis Pharma, a dynamic and collaborative international team focused on biopharmaceuticals.
- Mitarbeitervorteile: Gain hands-on experience in a regulated environment with opportunities for growth and learning.
- Warum dieser Job: Perfect for those seeking to make an impact in drug commercialization while working with cutting-edge technology.
- Gewünschte Qualifikationen: Technical training and ideally 3-5 years of lab experience; attention to detail is a must.
- Andere Informationen: Strong communication skills in English required; German is a plus.
Das voraussichtliche Gehalt liegt zwischen 36000 - 60000 € pro Jahr.
Purpose of your Job
We are seeking a highly motivated and detail-oriented Technical Assistant to join our GMP Group at Coriolis Pharma. In this role, you will assist our scientific team by performing routine tasks under GMP regulations to support client projects and analytics as part of the commercialization process of their drug products. This position is ideal for individuals looking to gain hands-on experience in a regulated laboratory environment while working on a variety of client-driven projects within a dynamic, international and collaborative team.
Your Responsibility
- Support Client Projects: Assist scientists with the preparation and execution of routine analytical testing methods, such as chromatography, spectroscopy, and other standard assays for client projects under GMP regulations.
- Sample Handling: Support the preparation and handling of samples for testing, including labeling, storage, and tracking of materials used in client projects.
- Data Entry: Enter test results and other relevant data into project-specific databases or laboratory information management systems (LIMS) following appropriate protocols.
- Collaboration with Scientists: Work collaboratively and closely with project teams to support the efficient execution of client projects and provide any additional support required for project progression.
- GMP Compliance: Ensure all tasks are completed in strict adherence to GMP guidelines, following standard operating procedures (SOPs) and ensuring proper documentation of activities.
- Documentation and Reporting: Maintain accurate records of analytical processes, results, and materials used. Assist in the preparation of project documentation and analytical reports for clients.
What you need to succeed
- Technical training (e.g., CTA, PTA, MTA, or similar qualification).
- Ideally, 3-5 years of experience in a laboratory environment, preferably in a GMP-regulated setting. Experience in the biopharmaceutical industry is a plus.
- Basic understanding of GMP guidelines and regulatory requirements in the pharmaceutical industry.
- Ability to perform repetitive tasks with high attention to detail, ensuring accuracy in all steps of the analytical process.
- Strong organizational skills and the ability to manage multiple tasks and priorities efficiently.
- Basic knowledge of laboratory instruments and analytical techniques.
- Strong communication skills in English (German is a plus) and the ability to work effectively in a team environment.
- Proficient in Microsoft Office Suite; experience with laboratory information management systems (LIMS) is an advantage.
Your Contact
Dominik Schwemmer
Senior Business Partner – Talent & Development
People, Organization & Culture Unit
Coriolis Pharma Research GmbH
Phone: +49 (0) 89 – 417760 – 0
Fraunhoferstraße 18 b, 82152 Martinsried
#J-18808-Ljbffr
Technical Assistant – GMP Group (f/m/d) Arbeitgeber: Coriolis Pharma
Kontaktperson:
Coriolis Pharma HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Technical Assistant – GMP Group (f/m/d)
✨Tip Number 1
Familiarize yourself with GMP regulations and guidelines. Understanding these standards is crucial for the Technical Assistant role, as you'll be working in a regulated laboratory environment. This knowledge will not only help you during the interview but also demonstrate your commitment to compliance.
✨Tip Number 2
Gain hands-on experience with analytical techniques like chromatography and spectroscopy. If you can showcase any practical experience or projects where you've used these methods, it will significantly strengthen your application and show that you're ready to hit the ground running.
✨Tip Number 3
Highlight your organizational skills and ability to manage multiple tasks. In this role, you'll need to juggle various responsibilities, so providing examples of how you've successfully managed similar situations in the past will make you stand out.
✨Tip Number 4
Brush up on your communication skills, especially in English. Since you'll be collaborating with an international team, being able to communicate effectively is key. Consider practicing common scientific terminology and phrases that might come up in discussions.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Technical Assistant – GMP Group (f/m/d)
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Technical Assistant position. Highlight key responsibilities and required qualifications that align with your experience.
Tailor Your CV: Customize your CV to emphasize relevant technical training and laboratory experience, particularly in GMP-regulated environments. Include specific examples of analytical techniques you have used.
Craft a Strong Cover Letter: Write a cover letter that showcases your motivation for applying to Coriolis Pharma. Mention your attention to detail, organizational skills, and ability to work collaboratively in a team setting.
Highlight Relevant Skills: In your application, make sure to highlight your understanding of GMP guidelines, experience with laboratory instruments, and proficiency in Microsoft Office Suite. If applicable, mention any experience with LIMS.
Wie du dich auf ein Vorstellungsgespräch bei Coriolis Pharma vorbereitest
✨Understand GMP Regulations
Make sure you have a solid understanding of Good Manufacturing Practice (GMP) regulations. Be prepared to discuss how you have adhered to these guidelines in your previous roles, as this will demonstrate your commitment to quality and compliance.
✨Showcase Your Technical Skills
Highlight your technical training and any relevant laboratory experience. Be ready to talk about specific analytical techniques you are familiar with, such as chromatography or spectroscopy, and how you've applied them in a lab setting.
✨Emphasize Attention to Detail
Since the role requires high attention to detail, prepare examples from your past work where your meticulousness made a difference. Discuss how you ensure accuracy in data entry and sample handling, which are crucial for GMP compliance.
✨Demonstrate Team Collaboration
This position involves working closely with scientists and project teams. Be prepared to share experiences that showcase your ability to collaborate effectively, manage multiple tasks, and communicate clearly within a team environment.
