MPharma Associate Scientist Job at Syngene, Apply Online
We are hiring! If you wish to be part of a dynamic, high-performing team for bringing new solutions to drug discovery and changing people’s lives for the better, please read more. We are looking for Associate Scientist: In vitro Bioanalytical, for our DMPK team (Discovery Biology).
The five possible interview questions that can be asked in the technical round for the Associate Scientist: In vitro Bioanalytical job are posted below
◆Qualifications and Experience:
⦿MPharma with 3-8 years of experience/ MSc with 5-8 years of experience
⦿Looking for experience only in invitro Bioanalytical and method development& validation.
⦿Excellent communication and stakeholder management skills are a must.
⦿The candidate should have an excellent understanding of the fundamentals in handling, and troubleshooting LCMS/MS, LCHRMS/MS, and supporting ADME screening assays bioanalysis.
◆Job Location: Hyderabad
◆Last date to apply: 29th June 2023
◆Interested candidates may please visit: https://lnkd.in/dqtPQ375 or share your resume to [email protected].
Here are five possible interview questions that can be asked in the technical round for the Associate Scientist: In vitro Bioanalytical job:
- Question: Can you describe your experience in in vitro bioanalytical method development and validation? Answer: I have a Master’s degree in Pharmacy with 3-8 years of experience in in vitro bioanalytical methods. Throughout my career, I have been involved in developing and validating methods for analyzing drugs and their metabolites using LCMS/MS and LCHRMS/MS techniques. I have a strong understanding of the fundamentals and have successfully applied these techniques in ADME screening assays bioanalysis.
- Question: How do you handle and troubleshoot LCMS/MS and LCHRMS/MS instruments in a laboratory setting? Answer: I have extensive experience in handling LCMS/MS and LCHRMS/MS instruments. I ensure proper maintenance, calibration, and troubleshooting of these instruments to obtain accurate and reliable results. I am familiar with routine instrument checks, troubleshooting common issues, and collaborating with technical support if needed to resolve any complex problems.
- Question: Can you discuss your stakeholder management skills and how they have contributed to successful bioanalytical projects? Answer: Stakeholder management is crucial for effective collaboration and project success. I have excellent communication skills, which enable me to effectively interact with cross-functional teams, clients, and external partners. I prioritize clear and regular communication, actively listen to stakeholders’ requirements, and ensure their expectations are met. This approach has helped foster strong working relationships and contributed to successful bioanalytical projects.
- Question: How do you ensure compliance with regulatory guidelines and quality standards in in vitro bioanalysis? Answer: Compliance with regulatory guidelines and quality standards is of utmost importance in bioanalysis. I stay updated with the latest regulatory requirements, such as GLP and GCP, and ensure our laboratory practices and documentation adhere to these standards. I maintain accurate records, follow standard operating procedures, perform regular quality control checks, and participate in internal and external audits to ensure compliance and data integrity.
- Question: Can you provide an example of a challenging bioanalytical project you have worked on and how you overcame obstacles to achieve successful outcomes? Answer: Certainly. In a previous project, we were tasked with developing a sensitive LCMS/MS method for quantifying a low-abundance drug metabolite in complex biological matrices. We encountered challenges related to matrix interference and analyte stability. To overcome these obstacles, I collaborated with colleagues to optimize sample preparation techniques, implement suitable extraction strategies, and validate the method according to industry standards. By employing a systematic approach and troubleshooting at each step, we successfully achieved accurate and reliable quantification of the target metabolite.
Remember to provide specific examples from your experience and emphasize your ability to handle instruments, adhere to regulations, and effectively communicate with stakeholders. Good luck with your interview!
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