Pharmaceutical Product Testing Scientist

As a Pharmaceutical Product Testing Scientist at Eurofins Scientific, your key responsibilities will include performing various types of testing using advanced chromatographic systems, executing specialized analyses, troubleshooting method and instrumentation issues, documenting your work for GMP compliance, and producing detailed reports for clients. You will also be involved in developing validation plans and training technical staff, contributing to the overall efficiency of our laboratory operations.

To qualify for the Pharmaceutical Product Testing Scientist position at Eurofins Scientific, you should possess a Bachelor's or Master's degree in chemistry or a related field, along with 3-5 years of laboratory experience. Experience in a cGMP environment and using EMPOWER and HPLC is highly valued. Additionally, having authorization to work in the United States without sponsorship is essential for this role.

Candidates with 3-5 years of transferable laboratory experience are preferred for the Pharmaceutical Product Testing Scientist position at Eurofins Scientific. This experience should ideally include working in a cGMP environment, utilizing various analytical techniques, and having a solid foundation in method validation and testing procedures.

As a Pharmaceutical Product Testing Scientist at Eurofins Scientific, you will receive comprehensive training on our specific methods, protocols, and instrumentation practices. You’ll also have opportunities for professional development, mentorship from experienced team members, and continuous learning in a rapidly evolving laboratory environment.

Yes, the position of Pharmaceutical Product Testing Scientist at Eurofins Scientific is a full-time role, typically from Monday to Friday, 8 am to 4 pm. We offer excellent full-time benefits, including comprehensive medical coverage, 401(k) with company matching, and paid vacation, making it an attractive opportunity for those looking to excel in their careers.

In preparing for this question, emphasize your hands-on experience with HPLC systems—mention specific projects where you used HPLC for method development or testing. Illustrate your familiarity with troubleshooting and optimizing results, which are vital in ensuring accurate pharmaceutical testing at Eurofins Scientific.

Discuss your understanding of GMP principles and how you implement them in your daily tasks. Provide examples of how you've documented procedures, maintained accurate records, and adhered to quality control processes to ensure testing was compliant with regulatory standards.

Look for a specific instance where you faced a troubleshooting issue, whether with instrumentation or analytical methods. Discuss the steps you took to diagnose the problem, the solution you implemented, and the outcome. This will showcase your problem-solving skills and ability to work under pressure.

Explain the key components of method validation, including specificity, accuracy, precision, and robustness. Relate your past experiences with validation protocols and highlight how you would adapt or create validation plans for the unique testing methodologies at Eurofins Scientific.

Demonstrate your commitment to professional growth by mentioning specific resources you follow, such as scientific journals, webinars, or industry conferences. Discuss how you apply newfound knowledge to your work and enhance testing methodologies at Eurofins Scientific.

Detail any experience with different chromatographic methods such as TLC, IC, or GC. Explain how you’ve applied these techniques in past roles, covering the types of analyses performed and insights gained from using these systems.

Share your systematic approach to documentation, emphasizing the importance of detailed, accurate entries in laboratory notebooks, compliance with SOPs, and your role in maintaining data integrity. Explain how thorough documentation contributes to traceability and overall quality assurance.

Discuss your experience in training junior staff or peers. Emphasize your communication skills, ability to create supportive learning environments, and willingness to share knowledge about lab procedures and safety protocols to foster continuous improvement within the team.

Talk about your experience with laboratory information management systems, such as EMPOWER, and how you've utilized data analysis software for reporting and compliance purposes. Highlight how these tools improve the efficiency and accuracy of lab operations.

Convey your passion for pharmaceuticals and the desire to contribute to public health and safety. Highlight your admiration for Eurofins' commitment to quality and innovation in testing and how your skills align with the company’s mission and values.