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Zydus Lifesciences Executive Production Supervisor Interview Questions and Answers
Zydus Lifesciences Executive Production Supervisor Interview Experiences
1 interview found
I applied via Walk-in and was interviewed before Jul 2021. There were 3 interview rounds.
Leak test inprocess missing during batch manufacturing.
(2 Questions)
- Q1. Aseptic practices and behaviour
- Ans. Maintain the Aseptic conditions by controlling the man, material and movement in Aseptic area.
- Q2. How to handle the intervention during Aseptic filling
- Ans.
Interventions during aseptic filling can be handled by following strict protocols, training staff, and implementing quality control measures.
Establish strict protocols for aseptic filling procedures
Train staff on proper aseptic techniques and interventions
Implement quality control measures to ensure compliance
Regularly monitor and evaluate interventions to identify areas for improvement
Maintain a clean and sterile envi...
Interview Preparation Tips
To help Improved my technical as well as compliance skill
Interview questions from similar companies
(6 Questions)
- Q1. Handling of Validation
- Ans.
Validation in production involves ensuring that processes and products meet quality standards.
Validation involves verifying that equipment, processes, and systems are operating correctly and consistently.
Validation also includes confirming that products meet specifications and quality standards.
Documentation of validation activities is essential for regulatory compliance and continuous improvement.
Examples of validatio...
- Q2. Operations of reactors, centrifuge, sparker filters, anfds, ejectors.
- Q3. Handling of Qualifications
- Q4. Handling of Safety permits
- Ans.
Safety permits are essential for ensuring compliance with regulations and maintaining a safe work environment.
Safety permits are required for certain activities or equipment to ensure they meet safety standards.
Production officers must be familiar with the types of safety permits needed in their industry.
They are responsible for obtaining and renewing safety permits as needed.
Failure to comply with safety permit requir...
- Q5. Operation of Distillation
- Ans.
Distillation is a process used to separate components of a liquid mixture based on differences in boiling points.
Distillation involves heating the liquid mixture to create vapor, then cooling the vapor to condense it back into liquid form.
The components with lower boiling points will vaporize first and be collected as the distillate, while the components with higher boiling points remain in the original container.
Commo...
- Q6. Handling of Deviations
- Ans.
Deviations in production processes must be promptly identified, investigated, and documented to ensure product quality and compliance.
Deviation should be reported immediately to the appropriate personnel
Investigate the root cause of the deviation
Document all findings and actions taken
Implement corrective and preventive actions to prevent recurrence
Review and approve deviation reports before closure
(5 Questions)
- Q1. Handling of CAPA
- Ans.
CAPA refers to Corrective and Preventive Actions taken to address non-conformities and prevent recurrence.
Identify the root cause of the issue
Develop a corrective action plan to address the issue
Implement the corrective action plan
Monitor the effectiveness of the corrective action
Implement preventive actions to prevent recurrence
- Q2. What is DATA INTIGRIY
- Ans.
Data integrity refers to the accuracy, consistency, and reliability of data throughout its lifecycle.
Ensuring data is accurate and reliable
Maintaining consistency of data
Preventing unauthorized access or modifications
Implementing data validation processes
Regularly backing up data to prevent loss
- Q3. Handling Solvents
- Q4. Handling of Batch failures
- Ans.
Batch failures should be analyzed to identify root causes and prevent future occurrences.
Investigate the root cause of the batch failure
Implement corrective actions to prevent future failures
Document the findings and actions taken for future reference
Communicate with relevant stakeholders about the batch failure and resolution
Conduct a review of the production process to identify potential areas for improvement
- Q5. Handling of Deviations
- Ans.
Handling of deviations involves identifying, investigating, and resolving any deviations from standard procedures or specifications.
Deviation should be documented and reported immediately
Investigate root cause of deviation
Implement corrective and preventive actions
Review and update procedures to prevent future deviations
(3 Questions)
- Q1. Current Role and responsibilities
- Q2. Personal information
- Q3. Salary discussion
Interview Preparation Tips
2. Safety and MSD
3.why shifting is required
4.What is the importance of blending
5 type of GMP practices you are following
6. Information from BMR
How dis lation happen
7. About MSDS
8. Why work permit system is required
9. Difference between incident and accident:
10.Work permits
*1)* What is GMP/cGMP as per your understanding? OR What do you know about GMP/cGMP?
*2)* What is Data Integrity?
Explain it with Examples.
*3)* What is Data Manipulation?
Explain with Examples.
*4)* What is meaning of Plant Capacity / Bottleneck / Equipment / Stage..?
*5)* Safety or Process Safety related to your Products.
What/Which kind of Safety Policy do you have in your current company?
*6)* ALCOA
PPE
PH
Chilled water temp
Deviation
GMP
EHS
Process
Operations
Current role and responsibilities
Solvent
Batch fail
CAPA
Validation, qualifications
Skills evaluated in this interview
Production Manager Interview Questions & Answers
Sun Pharmaceutical Industries
Anonymous
posted on 16 Jul 2024
(5 Questions)
- Q1. Tell me about DCS HMI
- Q2. How to manage manpower &cost reduction
- Ans.
Manpower can be managed by proper planning, training, and delegation. Cost reduction can be achieved through efficiency improvements, waste reduction, and negotiation with suppliers.
Develop a detailed manpower plan based on workload and skill requirements
Invest in training and development programs to upskill existing employees
Delegate tasks effectively to ensure optimal use of manpower
Implement efficiency improvements ...
- Q3. About documentation
- Q4. Production planning
- Q5. Batchprocess with safety
- Ans.
Batch process with safety involves ensuring that production processes are carried out in a safe and controlled manner.
Implementing safety protocols and procedures for each step of the batch process
Regularly conducting safety audits and inspections to identify potential hazards
Providing proper training to employees on safety measures and emergency procedures
Using appropriate personal protective equipment (PPE) when hand...
(2 Questions)
- Q1. Area qualifications
- Q2. Equipment validation
(2 Questions)
- Q1. Manufacturing process
- Q2. Trouble shooting
Production Officer Interview Questions & Answers
Torrent Pharmaceuticals
Anonymous
posted on 13 Aug 2024
Selected
I applied via Campus Placement
(2 Questions)
- Q1. What is the disintegration time of uncoated table
- Q2. What is the role of vent filter in rmg
- Ans.
Vent filter in RMG plays a crucial role in preventing contamination and maintaining the required air flow.
Vent filter helps in maintaining the required air flow in the RMG machine.
It prevents contamination by filtering out dust, particles, and other impurities from entering the machine.
Regular maintenance and replacement of vent filters are necessary to ensure optimal performance.
Vent filter also helps in maintaining t...
Interview Preparation Tips
(2 Questions)
- Q1. What is Granulation
- Ans.
Granulation is a process in which small particles are formed by agglomerating powder particles.
Granulation involves the binding of powder particles to form larger particles.
It is commonly used in pharmaceutical manufacturing to improve flow properties and reduce dust.
There are different methods of granulation such as wet granulation and dry granulation.
- Q2. Expalin 6M in deviation
- Ans.
6M in deviation refers to the factors that can cause a process to deviate from its intended outcome.
6M stands for Man, Machine, Material, Method, Measurement, and Mother Nature.
These factors can contribute to variations in production processes.
For example, a machine malfunction (Machine) can lead to deviations in product quality.
Addressing each of the 6M factors can help minimize deviations and improve overall producti
Interview Preparation Tips
I applied via Campus Placement and was interviewed in Jun 2024. There was 1 interview round.
(2 Questions)
- Q1. What is your project
- Q2. What is molarity
Interview Preparation Tips
(4 Questions)
- Q1. Give me information about your company
- Q2. What is benifit for employees?
- Ans.
Employee benefits include health insurance, retirement plans, paid time off, and professional development opportunities.
Health insurance coverage for employees and their families
Retirement plans such as 401(k) matching contributions
Paid time off for vacation, sick leave, and holidays
Professional development opportunities like training programs and tuition reimbursement
Employee discounts on company products or services
- Q3. Why are you not selecting every peoples?
- Q4. What is your selection process?
(2 Questions)
- Q1. Appearance of interviewer
- Q2. Self introduction
Interview Preparation Tips
Production Officer Interview Questions & Answers
Cadila Pharmaceuticals
Anonymous
posted on 15 Dec 2023
I applied via Walk-in and was interviewed in Nov 2023. There were 4 interview rounds.
Ok ok ok ok aptitude test
(2 Questions)
- Q1. About daily Process work
- Q2. Process handlled,
(2 Questions)
- Q1. Daily process ok
- Q2. Daily process ok ok
Interview Preparation Tips
Production Officer Interview Questions & Answers
Glenmark Pharmaceuticals
Anonymous
posted on 31 May 2024
Selected
I applied via Walk-in and was interviewed in Dec 2023. There was 1 interview round.
(2 Questions)
- Q1. How do you handle operation of reactor, centrifuge etc
- Ans.
I handle operation of reactor, centrifuge etc by closely monitoring parameters, following standard operating procedures, and troubleshooting any issues.
Monitor parameters such as temperature, pressure, and flow rates regularly
Follow standard operating procedures for starting up, operating, and shutting down equipment
Troubleshoot any issues that arise during operation, such as leaks or malfunctions
Ensure proper maintena...
- Q2. How do you handle documents in pharma area
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Zydus Lifesciences Executive Production Supervisor Reviews and Ratings
based on 2 reviews
Rating in categories
|
Senior Executive
1.8k
salaries
|  ₹2.3 L/yr - ₹11.5 L/yr |
|
Assistant Manager
1.7k
salaries
| ₹4.1 L/yr - ₹16.5 L/yr |
|
Executive
1.2k
salaries
| ₹2.3 L/yr - ₹8.8 L/yr |
|
Deputy Manager
885
salaries
| ₹5.8 L/yr - ₹18.5 L/yr |
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Officer
826
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| ₹1.5 L/yr - ₹6 L/yr |
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