Baxter Pharma & Chemistry R&D Job Opening – Apply Online

ign: center;">Baxter Pharma & Chemistry R&D Job Opening – Apply Online

Baxter hiring Candidates with master’s in pharmacy and chemistry for the post of Stability R&D Scientist, VIPs job opening 2023, Stability R&D Scientist, VIPs job vacancy 2023. Pharmacy job opening 2023, Pharmacy Research job opening 2023. Baxter Pharma & Chemistry R&D Job Opening – Apply Online. Interested and eligible candidates may check out all the details

Possible interview questions for the technical round are posted below

Job Title: Stability R&D Scientist, VIPs

Req #: JR – 101534

Location: Bengaluru, Karnataka, India

Job Category: Research and Development

Summary

Baxter currently has an opening for a R&D Scientist with experience designing and leading formulation stability studies, both internally and at external contract labs. The role will also be responsible for performing product and process assessments related to stability.  The incumbent will work closely with Baxter’s Integrated Supply Chain Organization, supporting programs intended to gain efficiencies throughout Baxter’s diverse manufacturing network.

Essential Duties and Responsibilities

• Develops design strategies or research projects, which are non-routine within areas of expertise to address specific technical requirements of a project.
• Studies, designs and recommendations reflect impact by and to related disciplines.
• Displays a solid understanding of theories/practices utilized by other disciplines outside the primary area of expertise.
• Evaluate results relative to product requirements, definitions and/or program goals.
• Independently plan and execute a series of design and/or technical tasks that may not be well-defined, have multiple variables, and require advanced techniques within negotiated deadlines.
• Play a lead role in the evaluation, selection and adaptation of various techniques, which accomplish business objectives such as quality and cycle-time.
• Devise new approaches to complex problems through adaptations and modifications of standard technical principles. Incorporate new methods and technologies for improving existing or new products/processes.
• Maintain current knowledge of relevant QSRs and other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities.
• Develop budgets and activity schedules of limited scope.
• Develop an in-depth knowledge and understanding of GxP and related regulations and guidance.
• Maintain focus on meeting both external and internal customer expectations.
• Utilize appropriate statistical approaches/tools for therapeutic product expiration dating and limits verification in line with procedures and project priorities. Accurately assess results for validity and conformance to specifications.

Qualifications

• Fluent in English
• Bachelor’s degree in relevant scientific discipline (chemistry, pharmaceutical sciences) with 5-7 years’ experience or Masters degree with 3-5 years’ experience or PhD with 0-3 years’ experience.
• Possess relevant laboratory/technical, writing, and computer skills.
• A good understanding of ICH and cGxP practices.
• Effectively able to contribute on a project team.  Experience in working in global cross-functional teams and project management is a plus.
• Demonstrates flexibility and can shift gears comfortably.
• Ability to objectively assess, organize, and clearly communicate complex information.
• Interpret available information and make recommendations to resolve technical challenges.
• Appropriately prioritize assignments to meet project schedules

APPLY ONLINE

Possible interview questions for the technical round:

1. Can you describe your experience in designing and leading formulation stability studies? Share an example of a project where you successfully conducted such studies. Answer: Yes, I have extensive experience in designing and leading formulation stability studies. For instance, in my previous role, I was responsible for conducting stability studies on a new pharmaceutical product. I developed a comprehensive study design, including sample collection, storage conditions, and testing parameters. By closely monitoring the product’s stability over time, I was able to identify any potential degradation or changes in its properties.
2. How do you ensure that your product and process assessments related to stability align with the defined requirements and goals? Answer: When conducting product and process assessments related to stability, I first thoroughly review the defined requirements and goals. I then evaluate the results of my assessments against these specifications to ensure alignment. By closely analyzing the data and comparing it with the desired outcomes, I can determine if the product and process meet the stability requirements.
3. Can you provide an example of a situation where you had to devise new approaches or adapt existing techniques to solve complex stability-related problems? Answer: Certainly! In one instance, we encountered a stability issue with a pharmaceutical formulation that was affecting its shelf life. To address this problem, I researched and implemented a novel packaging solution that provided enhanced protection against environmental factors. By adapting existing packaging techniques and incorporating new methods, we were able to significantly improve the stability of the product.
4. How do you stay updated on relevant regulatory requirements and ensure compliance in your research, data collection, and reporting activities? Answer: I understand the importance of staying updated on regulatory requirements. I regularly review relevant guidelines, such as ICH and cGxP practices, to ensure compliance. Additionally, I actively participate in professional development activities, attend seminars, and engage with regulatory bodies to stay informed about any changes or updates. By incorporating these practices, I ensure that my research, data collection, and reporting activities adhere to the latest regulatory standards.
5. Can you describe your experience in working as part of global cross-functional teams and managing projects? How do you prioritize assignments to meet project schedules? Answer: Throughout my career, I have had the opportunity to work in global cross-functional teams and manage projects. In these roles, effective communication and collaboration were key. I actively contributed my expertise, coordinated with team members from various regions, and ensured that project milestones were met. To prioritize assignments, I analyze the project requirements, assess the criticality and urgency of each task, and allocate resources accordingly. By maintaining a clear understanding of project schedules and deadlines, I can effectively prioritize assignments and deliver results on time.

Note: The answers provided here are general examples and can be tailored to reflect the interviewee’s specific experiences and expertise.

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