Pfizer MSc Chemistry Associate Scientist Vacancy - Apply Online

Pfizer MSc Chemistry Associate Scientist Vacancy – Apply Online

Dont forget to check out possible interview questions for this job below

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Job Title: Associate Scientist – API/Intermediate Process Development

Location: India – Chennai

Id: 4878281

Eligbility Criteria:

M.Sc Chemistry – 1 – 3 years relevant experience , freshers also welcome

Basic computer literacy, Experience in Pharmaceutical industry

Planning and executing the experiments

• Interpretation of experimental results and propose process improvements

• Preparing reports on project status and updating regularly

• Support for documentation and involvement in lab activities

• Time management and Good Documentation practices

• Training and adhering to cGMP procedures

• Training and adhering to Safety procedure

Literature search for alternative route of synthesis for intermediates, API and impurities (Safe, Cost effective and robust – process).

Supporting KGL/TT/MS&T departments for Technology transfer at manufacturing scale in plant and in resolving all the issues during scale up and suggest modifications in order to develop a scalable and robust process

Apply Online

Important Interview Questions and Answers for the above job role:

  1. What experience do you have in the Pharmaceutical industry?

Answer: I have a total of 2 years of experience in the Pharmaceutical industry, where I have worked on process development and optimization for small molecule drug substances. I have also worked on technology transfer projects, where I have supported manufacturing scale-up activities.

2. Can you explain your experience in literature search for alternative routes of synthesis for intermediates, API, and impurities?

Answer: In my previous role, I have conducted extensive literature searches for alternative routes of synthesis for intermediates and API. I focused on finding safe, cost-effective, and robust processes that can be easily scaled up to the manufacturing level. During this process, I analyzed a wide range of published research papers, patents, and other scientific literature.

3. How do you approach planning and executing experiments?

Answer: My approach to planning and executing experiments involves breaking down the experiment into smaller, manageable tasks, and ensuring that I have all the necessary equipment, reagents, and protocols before beginning. I also keep detailed notes and documentation of the experiment, including the experimental design, raw data, and any observations or results. This approach helps me stay organized, efficient, and focused.

4. What is your experience in adhering to cGMP procedures and Safety procedures?

Answer: As a scientist in the pharmaceutical industry, I have received extensive training on cGMP procedures and safety protocols. I have experience working in a cGMP compliant laboratory environment, adhering to good documentation practices, and ensuring that my work is compliant with regulatory standards. I also have experience working with hazardous materials and following all safety procedures to ensure a safe work environment for myself and my colleagues.

5. Can you explain your experience in supporting technology transfer at manufacturing scale in the plant?

Answer: In my previous role, I have supported technology transfer projects by providing technical expertise and guidance during manufacturing scale-up activities. This included troubleshooting and resolving any issues that arose during the scale-up process, suggesting modifications to the process to improve scalability and robustness, and ensuring that the process met the necessary regulatory and quality standards. I also assisted in preparing the necessary documentation and reports to support technology transfer and regulatory submissions.

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