Finde einen Job 
Finde eine Ausbildung 
Top Arbeitgeber 
Top Universitäten 
Für Unternehmen Auf einen Blick
- Aufgaben: Join our team as an Analyst focusing on GMP and analytical tasks.
- Arbeitgeber: Eurofins Scientific is a global leader in analytical testing services for various industries.
- Mitarbeitervorteile: Enjoy extensive training, a dynamic work environment, and an attractive salary package.
- Warum dieser Job: Be part of impactful projects that ensure product safety and authenticity while growing your skills.
- Gewünschte Qualifikationen: Bachelor/Master/PhD in relevant fields with 2+ years lab experience and knowledge of ELISA methods.
- Andere Informationen: This is a limited 1-year contract with opportunities for personal development.
Das voraussichtliche Gehalt liegt zwischen 36000 - 60000 € pro Jahr.
BIOPHARMA SERVICES Method Validation- Analyst (M/W/D)
2 days ago Be among the first 25 applicants
Company Description
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services.
Job Description
For one of our teams based in Heidelberg we are currently looking to hire an Analyst with a focus on GMP, and to support technical and Analytical tasks. Your main responsibilities will include, but are not limited to:
- Responsible for analytical investigations and problem-solving activities
- Performance of classical ELISA methods
- Writing of analytical documents linked to the method validation
- Support of Validation / qualification of analytical equipment
- Knowledge of HPLC and chromatography methods
- Writing of analytical documents like method validation protocols and reports for standard analytical methods in English
- Ensuring that clients\‘ requirements are fully met.
Qualifications
- Bachelor / Master degree or PhD in analytical or pharmaceutical science or biochemistry/food chemistry
- 2+ years’ experience in a laboratory environment
- Must understand the ELISA methods and additional analytical methods
- Professional Experience in working on GMP
- Excellent communication (oral and written) and attention to detail
- Familiarity with pharmaceutical and/or laboratory operations (spectrophotometers, electrophoresis equipment, ELISA plate readers, and other laboratory equipment)
- Good planning, organizational and troubleshooting skills
Additional Information
We are offering you an interesting position within a truly global company. After several onboarding trainings, to make sure you have the experience you need, you will be working independently in our team.
- Limited 1 year contract with Eurofins PSS
- Integration in a fast-growing international company with a dynamic working environment and a good team spirit where personal development and growth are encouraged
- Extensive on-the-job coaching & training with clear areas of responsibility
- An attractive salary package
- Interesting client projects
If this position could be of interest to you or if you have any questions regarding this position, please feel free to reach out to Dhivi Sanghi ( ), Talent Attraction specialist Eurofins PSS Germany and Austria.
Please note that as per Eurofins policy, we do not accept unsolicited resumes from third-party recruiters unless such recruiters were engaged to provide candidates for a specified opening.
Seniority level
- Entry level
Employment type
- Full-time
Job function
- Quality Assurance
- Research
#J-18808-Ljbffr
BIOPHARMA SERVICESMethod Validation- Analyst (M/W/D) Arbeitgeber: Eurofins Optimed Clinical Research
Kontaktperson:
Eurofins Optimed Clinical Research HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: BIOPHARMA SERVICESMethod Validation- Analyst (M/W/D)
✨Tip Nummer 1
Nutze dein Netzwerk! Sprich mit ehemaligen Kollegen oder Kommilitonen, die bereits in der Biopharma-Branche arbeiten. Sie können dir wertvolle Einblicke geben und möglicherweise sogar eine Empfehlung aussprechen.
✨Tip Nummer 2
Informiere dich über Eurofins Scientific und deren spezifische Projekte im Bereich der Method Validation. Zeige in deinem Gespräch, dass du ein echtes Interesse an ihren Dienstleistungen und Werten hast.
✨Tip Nummer 3
Bereite dich auf technische Fragen vor, insbesondere zu ELISA-Methoden und HPLC. Du solltest in der Lage sein, deine Erfahrungen und Kenntnisse in diesen Bereichen klar und präzise zu erläutern.
✨Tip Nummer 4
Zeige deine Teamfähigkeit und Kommunikationsfähigkeiten während des gesamten Bewerbungsprozesses. Eurofins legt großen Wert auf gute Zusammenarbeit, also sei bereit, Beispiele für erfolgreiche Teamprojekte zu teilen.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: BIOPHARMA SERVICESMethod Validation- Analyst (M/W/D)
Tipps für deine Bewerbung 🫡
Understand the Job Requirements: Carefully read the job description to understand the specific qualifications and responsibilities. Highlight your relevant experience in analytical methods, especially ELISA and HPLC, in your application.
Tailor Your CV: Customize your CV to reflect your educational background and professional experience that aligns with the role. Emphasize your laboratory experience and any GMP knowledge you possess.
Craft a Strong Cover Letter: Write a cover letter that showcases your passion for biopharma services and your problem-solving skills. Mention specific examples of your work with analytical methods and how you can contribute to Eurofins.
Proofread Your Application: Before submitting, thoroughly proofread your CV and cover letter for any grammatical errors or typos. Ensure that all information is clear and professionally presented, as attention to detail is crucial in this field.
Wie du dich auf ein Vorstellungsgespräch bei Eurofins Optimed Clinical Research vorbereitest
✨Understand ELISA and Analytical Methods
Make sure you have a solid understanding of ELISA methods and other analytical techniques. Be prepared to discuss your experience with these methods in detail, as they are crucial for the role.
✨Showcase Your GMP Knowledge
Since the position emphasizes working under Good Manufacturing Practices (GMP), be ready to explain how you've applied GMP principles in your previous roles. Highlight any specific experiences that demonstrate your compliance with these standards.
✨Prepare for Technical Questions
Expect technical questions related to method validation and analytical investigations. Brush up on your knowledge of HPLC and chromatography methods, and be ready to discuss how you've used them in past projects.
✨Communicate Clearly and Effectively
Strong communication skills are essential for this role. Practice articulating your thoughts clearly, both verbally and in writing. Be prepared to provide examples of how you've effectively communicated complex information in previous positions.
