Best Job opportunity in Cadila Pharma.
Cadila Pharma Limited is conducting a walk-in drive for several departments (ADL, PERL, Synthesis, and RA) at its Dholka Plant on February 15, 2015. If you’re interested, it would be a great opportunity to apply for relevant positions.
| Table of contents |
|---|
| 1. Company Profile |
| 2. Vacancy Details |
| 3. Walk-In interview details |
| 4. Mandatory Documents |
| 5. Interview Questions Answer For Interview |
| 6. Important Link |
1. Cadila Pharma Company Profile:
Cadila Pharmaceuticals, also known as Zydus Cadila, is one of India’s leading pharmaceutical companies, with a focus on manufacturing generic drugs, biosimilars, and active pharmaceutical ingredients (APIs). The company is known for its extensive work in research and development and its commitment to improving healthcare.
As for its employees, Cadila Pharmaceuticals offers various opportunities for career growth and professional development. The company has initiatives aimed at creating a collaborative work environment and focuses on providing employees with the necessary resources for skills enhancement. Here are a few potential avenues for employees at Cadila :
- Training and Development:
- Health and Wellness Program
- Career Growth Opportunity
- Work Life balance
- Innovation and Research
2. Cadila Pharma Dholka Vacancy :
| Vacancy No : 01 | |
|---|---|
| Department | ADL |
| Position | Research Associate / Deputy manager / Principal Scientist |
| Qualification | MSC chemistry |
| Experience | 3 to 7 years |
| Vacancy No : 02 | |
|---|---|
| Department | PERL |
| Position | Trainee Scientist / Research Associate |
| Qualification | Diploma / BE / BTech (chemical) |
| Experience | 1 to 5 years |
| Vacancy No : 03 | |
|---|---|
| Department | Synthesis |
| Position | Research Associate / Sr. Research Associate |
| Qualification | MSc organic chemistry |
| Experience | 3 to 7 years |
| Vacancy No : 04 | |
|---|---|
| Department | Regulatory Affairs |
| Position | Officer / Senior officer |
| Qualification | MSc |
| Experience | 4 to 7 years ( RA API – Europe / Row) |
3. Cadila Pharma Walk-In interview Details :
Interview date : 15 -02-2025
Interview time : 9:30 to 4:00 pm
Interview location : IRM House, CG Road, Opp. Sardar Patel seva Samaj navrangpura Ahmedabad.
Contact Person : Shardulsinh Kathawadia.
Email : Shardulsinh.k@cadilapharma.com
4. Cadila Pharma Mandatory Documents during Interview :
- Updated Resume
- last 3 month salary proof
- Education proof
- One photograph
- Experience Document
5. Interview Questions Answer For Interview :
1. What are the key components of the ADL process?
Answer: The key components of the ADL process include:
Application Development: Writing, testing, and maintaining code to build the software solutions.
Application Maintenance: Ongoing support, bug fixing, performance optimization, and updating existing applications.
Documentation: Creating and maintaining technical and functional documentation for software systems.
User Support: Providing help to end-users and addressing issues in a timely manner.
Versioning: Managing and tracking different versions of the software to ensure smooth upgrades and deployments.
2. Can you describe a time when you had to resolve a high-priority issue in an application?
Answer: In one instance, a critical bug was discovered in a financial application that was causing incorrect data calculations during transactions.
The issue was flagged by users, and it needed immediate attention.
I first identified the root cause by reviewing logs and tracing the code flow. After pinpointing the problematic function, I developed a hotfix, thoroughly tested it in the development environment, and deployed it with minimal downtime.
I communicated the resolution to both the internal team and the affected users to ensure transparency and maintain trust.
3. What programming languages and tools are you proficient in?
Answer: I have worked with several programming languages and tools, including:
Languages: Java, C#, Python, and SQL.
Frameworks/Technologies: Spring Boot, ASP.NET, Angular, React.
Databases: MySQL, Oracle, PostgreSQL.
Version Control: Git, SVN.
CI/CD Tools: Jenkins, Bamboo.
Testing: JUnit, Selenium, Postman.
My experience includes both development and maintaining applications built using these technologies.
4. How do you stay updated with the latest trends in software development and maintenance?
Answer: To stay updated,
Regularly read technical blogs, research papers, and industry news websites like Stack Overflow, GitHub, and Medium.
Attend webinars, conferences, and meetups to learn from experts and network with peers.
Experiment with new tools, frameworks, and technologies in my personal projects or in a sandbox environment.
Participate in online courses and certifications to deepen my knowledge and stay ahead of new trends in the industry.
5. Tell us about your experience in regulatory affairs.
Answer: I have worked in Regulatory Affairs for the past 6 years, primarily focusing on the pharmaceutical and medical device sectors. I have been involved in the preparation and submission of INDs and NDAs, including the interaction with the FDA and EMA for product approvals. I have also managed post-market surveillance reports, ensuring that our products comply with evolving regulatory standards across multiple markets.
6. What do you consider to be the most challenging regulatory submission you have worked on, and how did you overcome the challenges?
Answer: One of the most challenging submissions was an NDA filing where we received multiple rounds of queries from the FDA about the product’s clinical trial data. It required significant collaboration between the clinical, safety, and regulatory teams to address these concerns thoroughly. I led the preparation of the responses and managed the timelines closely, ensuring that we provided comprehensive data. Ultimately, we successfully obtained approval on the second submission.
7. How do you prioritize regulatory tasks when working with multiple projects and deadlines?
Answer: I prioritize tasks by assessing the urgency and complexity of each project, making sure that I address regulatory submissions with the most immediate deadlines first. I use project management software to keep track of milestones and communicate regularly with other departments, such as clinical and manufacturing teams, to ensure that all necessary information is available and timelines are met.
8. What is your approach to risk management in regulatory affairs?
Answer: In Regulatory Affairs, I believe in identifying potential risks early in the submission process. I collaborate with cross-functional teams to anticipate any regulatory challenges, whether related to clinical data or manufacturing issues, and develop mitigation strategies. For instance, in a recent device submission, I identified a potential delay due to pending documentation, and by working with the regulatory and clinical teams, we were able to expedite the data collection and submission process.
9. How do you handle situations where a regulatory authority rejects a submission or requests a resubmission?
Answer: In the event of a rejection or request for resubmission, I carefully review the feedback provided by the regulatory agency. I work closely with the technical and clinical teams to address any concerns, whether related to data or compliance. One such case involved a clinical trial design issue raised by the FDA. After reviewing the comments, we adjusted the trial design and resubmitted it with additional supporting data, ultimately receiving approval.
10.How do you approach preparing regulatory submissions in a highly regulated market?
Answer: In highly regulated markets like the EU or the US, I ensure all regulatory requirements are fully met by carefully reviewing the guidance documents and applicable regulations. I coordinate with cross-functional teams to gather the necessary clinical, non-clinical, and manufacturing data. Additionally, I conduct thorough internal reviews to ensure that every aspect of the submission is compliant with the local regulatory framework.
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6. Important Link :
| Company Officials website | Click here |
| Latest job | Click here |
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