Chemistry and Mpharm job as Scientist

Chemistry and Mpharm job as Scientist at Zoetis. Interested candidates can apply now.

Job ID – 06132023

Job role – Sr. Associate Scientist / Scientist – Analytical R&D

Job Location – Navi Mumbai, India

About the Job provider –

Zoetis is a global animal health company dedicated to supporting customers and their businesses. Building on more than 60 years of experience, they deliver quality medicines, biopharmaceuticals and vaccines, complemented by diagnostic products and genetic tests and supported by a range of services. They are working every day to better understand and address the real-world challenges faced by those who raise and care for animals in ways they find truly relevant.


The incumbent will be responsible for supporting analytical research and development activities (method development, validations, transfers, documentation, stability, etc.) for drug products. The candidate will be responsible for supporting multiple projects and will work in close collaboration with partner groups across the organization such as global development teams (formulation, chemistry, safety sciences, etc.), regulatory, quality, manufacturing and clinical organizations as well as manage analytical activities outsourced to vendors. The candidate will be responsible for authoring, reviewing, and archival of various documentation such as specifications, test procedures, method validation plans

, protocols, reports, stability data, SOPs, and CMC technical sections for regulatory submission.

Essential skills/competencies

  • Good understanding, knowledge, and experience with various modern analytical tools and technologies used in the pharmaceutical industry (e.g., U/HPLC, GC, NMR, MS, Karl Fischer, dissolution, particle size, etc).
  • Practical analytical experience working with dosage forms including solids and liquids for oral, topical and parenteral administration. This includes demonstrated experience in the technical areas of stability, characterization/isolation of impurities, and a track record of analytical problem-solving.
  • Basic knowledge of degradation pathways stress stability designs, stabilization techniques, and biopharmaceutical aspects of drug products.
    Basic understanding of analytical quality requirements for clinical supplies and technology transfer activities.
  • Fair understanding of the pharmaceutical development process.
  • Basic knowledge of Quality by Design (QbD) principles and optimization techniques.
    Good interpersonal, communication and presentation skills are essential for contributing to project teams and influencing decisions.
  • Good documentation skills for recording research and ability to summarize results and data in concise memos, development reports, summaries etc.; experience in writing and supporting regulatory documents (e.g., validation reports, specifications, stability reports, development summaries, CMC technical sections).

Other attributes desirable for Chemistry and Mpharm job as Scientist –

  • Stay current with new developments in analytical chemistry and their application to development projects.
  • Use knowledge and experience to design, conduct and interpret data from experiments. Plan work independently based on specific objectives. Prioritize tasks; keep management/team informed of progress and adjust work accordingly. Display an understanding of project goals.
  • Demonstrate the ability to identify and recommend solutions for problems that arise in the course of experimentation.
  • Understand safety. Consider safety as an integral part of planning for and performing daily activities.
  • Communicate technical information efficiently and accurately. Practice active listening skills to understand the information being communicated by others. Deliver articulate presentations in a team environment. Write clearly and concisely. Maintain laboratory notebook meeting corporate standards.
  • Continuously improve techniques and work processes by introducing imaginative approaches and championing new technologies to improve group/team performance.
  • Recognize the importance of relationships within the work group. Build a sense of partnership with others in the workgroup to achieve results. Build and maintain a strong network with people from other departments to enhance collaboration on assignments.
  • Work as part of international teams, work with contract research organizations and have familiarity with the Animal Health industry.


M Pharm / M Sc in Analytical / Pharmaceutical Chemistry, or other related discipline with 4+ years of analytical research experience in Pharmaceutical R&D

Apply now

Hello there, We are providing some expected interview questions and answers for your reference. Please go through it during your preparation for Chemistry and Mpharm job as Scientist. Prepare and do well for your interview. All the very best!!!

Can you describe your experience with modern analytical tools and technologies used in the pharmaceutical industry?
Answer: Yes, I have extensive experience working with various analytical tools such as U/HPLC, GC, NMR, MS, Karl Fischer, dissolution, and particle size analyzers. I have utilized these technologies for method development, validation, and characterization of drug products in my previous roles. I stay updated with the latest advancements in analytical chemistry to ensure the application of the most suitable techniques for the projects I work on.

How have you applied your knowledge of stability studies and impurity characterization in your previous analytical research projects?
Answer: In my previous roles, I have designed and conducted stability studies to evaluate the degradation pathways and stability profiles of drug products. I have also focused on the isolation and characterization of impurities to ensure product quality and safety. By leveraging my analytical problem-solving skills, I have successfully identified and resolved any issues related to stability and impurity profiles during the development process.

Have you been involved in the authoring and reviewing of regulatory documents for pharmaceutical submissions?
Answer: Yes, I have extensive experience in writing and supporting regulatory documents such as method validation reports, specifications, stability reports, development summaries, and CMC technical sections. I understand the importance of regulatory compliance and have a strong grasp of the necessary documentation required for successful submissions. I ensure that all documents are accurate, concise, and in compliance with regulatory guidelines.

How do you prioritize tasks and manage multiple projects effectively?
Answer: Prioritizing tasks and managing multiple projects is crucial for successful project execution. I employ effective time management techniques such as creating project timelines, setting clear objectives, and breaking down tasks into manageable steps. By regularly communicating with stakeholders and team members, I stay informed of project progress and adjust work accordingly to meet deadlines. I am adaptable and can efficiently shift focus between projects based on their priority and urgency.

Can you provide an example of a time when you utilized your analytical skills to recommend innovative solutions to a complex problem?
Answer: In a previous project, we encountered challenges in the analysis of a novel drug formulation due to its complex matrix. I conducted extensive research on alternative analytical techniques and identified a new approach that involved modifying the sample preparation procedure and utilizing advanced spectroscopic methods. By implementing this innovative solution, we were able to overcome the analytical limitations and obtain accurate results. This experience showcases my ability to think critically, explore new technologies, and recommend effective solutions to complex problems.


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