Syngene MSc Biological Sciences & Biochem Research Job Opening, Apply Online
Syngene MSc Biological Sciences & Biochem Research Job Opening, Apply Online. MSc Biological Sciences Job in Syngene, Bangalore. Syngene is hiring MSc Biological Sciences candidates for a Senior Research Associate – Pharmacokinetics and Immunogenicity Assays job.
Don’t forget to check out possible interview questions for this job below
Designation: Senior Research Associate – Pharmacokinetics and Immunogenicity Assays
Job ID: 53986
Job Location: Bangalore
Department: Immunogenicity Research Laboratory
Job Purpose: The position holder is responsible for performing bioanalysis which includes performing ligand binding assays related to Pharmacokinetics and Immunogenicity.
Key Responsibilities:
- Ensure activities conducted in the bioanalytical lab are in compliance with established SOPs, procedures, systems, regulatory guidance without deviating from established procedures.
- Regular interaction and participation with Study director, Quality Control (QC) and Quality Assurance (QA) during raw data and reports review, closure of observations and archival.
• Ensure to complete the assigned tasks in timely manner.
• Prepare reagents, buffers and maintain log book for assigned assays
• Interpret results – anticipate and understand the issues related to the assay.
• Participate in, and present data for discussions.
• Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety.
• Attend training on environment, health, and safety (EHS) measures imparted company
Educational Qualification:
- Master’s degree in Biological Sciences (Preferably Biochemistry background) or a related field.
Technical/Functional Skills:
- Should have a strong background in immunoassay and bioanalytical Pharmacokinetics and Immunogenicity Assays with a good understanding as per regulatory guidance/ industry practices/internal Standard Operating Protocols.
- Should have hands-on experience in Ligand Binding Assay (LBA) development, validation and Sample analysis. Knowledge of ELISA and MSD assays are highly desirable.
- Knowledge and experience with regulatory requirements e.g. Organization for Economic Co-operation and Development (OECD), GXP, 21 CFR Part 11, European Medicines Agency (EMA) and Food and Drug Administration (FDA) guidelines.
Experience:
- 3-6 years of total experience in Pharmacokinetics and Immunogenicity Assays
Behavioural Skills:
- Should be independent.
- Excellent communication skills – written and oral in English
- Should have good interpersonal skills
- Large degree of flexibility and ability to work under strong time pressure
💡 Here are a few possible interview questions for the above job posting and their answers.
👍We hope this helps in giving you a rough idea as to how to prepare for the interview for this specific role. Good luck!
- Can you describe your experience with Ligand Binding Assay (LBA) development, validation, and sample analysis?
Answer: Yes, I have hands-on experience in LBA development, validation, and sample analysis. I have worked on a variety of LBA techniques and have a good understanding of regulatory guidance, industry practices, and internal Standard Operating Protocols.
- What is your experience with interpreting results and anticipating and understanding issues related to the assay?
Answer: I have extensive experience interpreting results and anticipating and understanding issues related to the assay. I have a strong background in immunoassay and bioanalytical Pharmacokinetics and Immunogenicity Assays, which has given me the necessary expertise to understand the various issues that may arise during the process.
- How do you ensure that activities conducted in the bioanalytical lab are in compliance with established SOPs, procedures, systems, regulatory guidance without deviating from established procedures?
Answer: I ensure that activities conducted in the bioanalytical lab are in compliance with established SOPs, procedures, systems, regulatory guidance without deviating from established procedures by regularly interacting and participating with Study director, Quality Control (QC) and Quality Assurance (QA) during raw data and reports review, closure of observations and archival.
- Can you describe your experience working with regulatory requirements such as Organization for Economic Co-operation and Development (OECD), GXP, 21 CFR Part 11, European Medicines Agency (EMA), and Food and Drug Administration (FDA) guidelines?
Answer: Yes, I have extensive knowledge and experience working with regulatory requirements such as OECD, GXP, 21 CFR Part 11, EMA, and FDA guidelines. I have worked on various projects that required strict adherence to these regulations, and I have the necessary expertise to ensure compliance with them.
- Can you describe a time when you had to work under strong time pressure?
Answer: Yes, I have worked under strong time pressure in the past. During one of my previous projects, we had to complete the analysis within a tight deadline. I prioritized the tasks and ensured that all the activities were completed on time while maintaining the quality standards. I have good interpersonal skills and can work well under pressure.
About Syngene
Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market, and lower the cost of innovation.
Equal Opportunity Employer:
It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status about public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
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