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J B Chemicals And Pharmaceuticals Executive Interview Questions and Answers
J B Chemicals And Pharmaceuticals Executive Interview Experiences
2 interviews found
(2 Questions)
- Q1. Formulation development process
- Ans.
The formulation development process involves creating and optimizing the composition of a product.
Identify the desired characteristics of the product
Select appropriate ingredients and their quantities
Conduct experiments to optimize the formulation
Test the stability and efficacy of the final product
Iterate on the formulation based on results
- Q2. ICH guidelines and stability study
Interview Preparation Tips
I applied via Company Website and was interviewed in Mar 2024. There was 1 interview round.
(1 Question)
- Q1. What is change control and its types.
- Ans.
Change control is the process of managing changes to a project or system in a controlled and systematic manner.
Change control involves documenting, evaluating, approving, and implementing changes to a project or system.
Types of change control include preventive, detective, and corrective.
Preventive change control aims to prevent issues before they occur, such as implementing quality assurance processes.
Detective change...
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(4 Questions)
- Q1. What action you take when Media Fail ?
- Ans.
When media fails, I assess the situation, communicate with stakeholders, and take appropriate corrective actions.
Assess the impact of the media failure on the organization
Communicate transparently with stakeholders about the situation
Identify the root cause of the failure and take corrective actions
Implement measures to prevent similar failures in the future
- Q2. Difference between API, BULK, and Formulation ?
- Q3. Why always c letter small in cGMP Guidelines ?
- Ans.
The 'c' in cGMP guidelines is always lowercase because it stands for 'current', not a proper noun.
The 'c' in cGMP stands for 'current', not a proper noun.
Lowercase 'c' emphasizes that the guidelines are constantly evolving and being updated.
It distinguishes cGMP guidelines from other specific guidelines or regulations.
Example: cGMP guidelines are designed to ensure the quality and safety of pharmaceutical products.
- Q4. Explain about ALCOA ++. and GDP.?
- Ans.
ALCOA++ is a data integrity framework used in regulated industries, while GDP refers to Gross Domestic Product.
ALCOA++ is a framework used in regulated industries to ensure data integrity, standing for Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, and Enduring.
GDP is a measure of a country's economic performance, representing the total value of all goods and services produced over a ...
Skills evaluated in this interview
(2 Questions)
- Q1. Inprocess checks in shop floor
- Q2. About change controls and Deviations
(2 Questions)
- Q1. What about previous experience
- Q2. Any achievements
Interview Preparation Tips
After compare with your previous organization and any other organization.
Don't join foolish way, think once.
(2 Questions)
- Q1. Detailed biodata of employee with previous organisations work
- Ans.
Employee has a diverse background with experience in multiple organizations.
Worked at ABC Company as a marketing manager for 5 years
Prior to that, worked at XYZ Corporation as a sales executive for 3 years
Has experience in both marketing and sales roles
- Q2. Subject matter matter expert for related all topics
(2 Questions)
- Q1. Tell me About yourself
- Ans.
I am a highly motivated and experienced executive with a proven track record of driving business growth and leading successful teams.
Over 10 years of experience in executive leadership roles
Strong strategic planning and decision-making skills
Proven ability to drive revenue growth and increase profitability
Effective team leader with a focus on collaboration and communication
- Q2. Explain Quality Risk Assessment
- Ans.
Quality risk assessment is a process used to identify, analyze, and evaluate potential risks that could impact the quality of a product or process.
Identify potential risks that could affect quality
Analyze the likelihood and impact of each risk
Evaluate the overall risk level and prioritize actions to mitigate
Implement risk mitigation strategies to reduce or eliminate identified risks
Monitor and review the effectiveness
Selected
I was interviewed in Dec 2024.
(1 Question)
- Q1. Can you tell me about yourself?
Abinash Bisoyi
Selected
I applied via Company Website and was interviewed in May 2024. There were 2 interview rounds.
(2 Questions)
- Q1. Abou working related
- Q2. Analysis related questions
(2 Questions)
- Q1. Introduction about self
- Q2. Salary discussion and Documents verification and qualification
Interview Preparation Tips
- Quality Control
- Section
Dablu Das
(3 Questions)
- Q1. Machine related questions and study related
- Q2. FFs hydraulic system related
- Q3. And aseptic behevior
Executive Interview Questions & Answers
Sun Pharmaceutical Industries
Anonymous
posted on 19 Feb 2024
(2 Questions)
- Q1. Related machine breakdown and performance
- Q2. Blister Packing machine
(1 Question)
- Q1. Ask for proper designation
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J B Chemicals And Pharmaceuticals Interviews By Designations
- J B Chemicals And Pharmaceuticals Medical Representative Interview Questions
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J B Chemicals And Pharmaceuticals Executive Interview Process
based on 2 interviews
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J B Chemicals And Pharmaceuticals Executive Reviews and Ratings
based on 18 reviews
Rating in categories
|
Medical Representative
154
salaries
|  ₹1.5 L/yr - ₹6 L/yr |
|
Officer
152
salaries
| ₹1.9 L/yr - ₹5.5 L/yr |
|
QC Officer
137
salaries
| ₹2 L/yr - ₹6 L/yr |
|
Executive
109
salaries
| ₹3 L/yr - ₹9.4 L/yr |
|
Production Officer
105
salaries
| ₹1.9 L/yr - ₹4.8 L/yr |
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