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Ipca Laboratories Production Officer Interview Questions and Answers
Ipca Laboratories Production Officer Interview Experiences
4 interviews found
(1 Question)
- Q1. What type of packaging products are available in pharmaceutical industry?
- Ans. Bulk packing, Pouch packing, Blister Packing, Packing, vial / injectable
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Selected
I applied via Approached by Company and was interviewed before Apr 2023. There were 2 interview rounds.
(3 Questions)
- Q1. What is gmp ?
- Q2. Why you left your job??
- Q3. What is deviation ?
- Ans.
Deviation refers to the act of departing from the usual or accepted standards, especially in a production process.
Deviation can occur when a product does not meet the specified requirements or standards.
It can also refer to a change in a process or procedure that was not authorized.
Deviation must be documented and investigated to determine the root cause and prevent recurrence.
Examples of deviation include using incorr...
(1 Question)
- Q1. Tell about your self ?
Selected
I applied via Recruitment Consulltant and was interviewed before Nov 2022. There were 2 interview rounds.
(5 Questions)
- Q1. Technical regarding experience
- Q2. Basic information about the subject matter
- Q3. Brief description of experience
- Q4. Details of machine regarding experience
- Q5. What is the purpose of leaving job
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Selected
I applied via Walk-in and was interviewed before Oct 2022. There were 3 interview rounds.
(2 Questions)
- Q1. Normal about yourself.
- Q2. Regarding regular duty.
(3 Questions)
- Q1. Technical questions
- Q2. Technical questions regarding machine.
- Q3. Documents review.
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(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
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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
(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...
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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
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I applied via Walk-in and was interviewed in Sep 2023. There was 1 interview round.
(8 Questions)
- Q1. Tell me about your self
- Ans. My name is Bhosale Dhiraj Pradip .I am 22 years old and. I complete my diploma in venutai Chavan pharmacy college phaltan. I am currently working in imaec medntek ltd in Rm,Pm stores Chinchwad pune and 14 months experience
- Q2. What are your strengths
- Q3. What are your salary expectation
- Q4. Explain granulation process
- Ans.
Granulation process involves the formation of granules from powder particles.
Powder particles are agglomerated to form granules.
Granulation can be achieved through wet or dry methods.
Wet granulation involves adding a liquid binder to the powder mixture.
Dry granulation involves compacting the powder mixture without the use of liquids.
Examples of granulation equipment include fluid bed granulators and roller compactors.
- Q5. Explain type of capsule
- Ans.
Capsules are solid dosage forms in which the drug is enclosed in a hard or soft soluble container.
Capsules can be classified as hard gelatin capsules or soft gelatin capsules.
Hard gelatin capsules are made of two pieces that fit together, while soft gelatin capsules are made of a single piece.
Capsules can be filled with powder, granules, pellets, or liquids.
Examples of capsules include Tylenol capsules and Vitamin E ca
- Q6. Two types of row material
- Ans.
Two types of row material are natural materials and synthetic materials.
Natural materials come from plants, animals, or minerals (e.g. cotton, wool, wood)
Synthetic materials are man-made through chemical processes (e.g. plastic, nylon, polyester)
- Q7. What Is your hobby
- Q8. Explain row material dispensing sicvence
- Ans.
Raw material dispensing science involves the accurate measurement and distribution of materials for production.
Raw material dispensing involves measuring and distributing materials needed for production processes.
Accurate measurements are crucial to ensure the quality and consistency of the final product.
Proper labeling and storage of raw materials is essential to prevent mix-ups and contamination.
Automated dispensing ...
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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
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Ipca Laboratories Production Officer Reviews and Ratings
based on 51 reviews
Rating in categories
|
Junior Officer
625
salaries
|  ₹1.5 L/yr - ₹4.5 L/yr |
|
Officer
542
salaries
| ₹1.7 L/yr - ₹5.9 L/yr |
|
Senior Officer
452
salaries
| ₹2.8 L/yr - ₹8 L/yr |
|
Research Associate
237
salaries
| ₹1.8 L/yr - ₹6.1 L/yr |
|
Executive
234
salaries
| ₹3.8 L/yr - ₹9.6 L/yr |
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