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Unichem Laboratories
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I applied via Approached by Company and was interviewed before Aug 2022. There were 3 interview rounds.
IPQA stands for In-Process Quality Assurance. It involves monitoring and inspecting the quality of products during the manufacturing process.
IPQA ensures that products meet quality standards at every stage of production
It involves conducting inspections, tests, and audits to identify and address any quality issues
IPQA helps in preventing defects and ensuring compliance with regulations and standards
Examples include che...
ECR/BPR/BCR stands for Engineering Change Request/Business Process Reengineering/Business Case Reengineering.
ECR (Engineering Change Request) is a formal proposal to make a change to a product's design or manufacturing process.
BPR (Business Process Reengineering) is the analysis and redesign of workflows within and between enterprises to optimize end-to-end processes and eliminate non-value-added tasks.
BCR (Business Ca...
Area or equipment clearance involves thorough cleaning and inspection to ensure safety and quality standards are met.
Start by removing all items from the area or equipment being cleared.
Clean the area or equipment using appropriate cleaning agents and tools.
Inspect the area or equipment for any damage, wear and tear, or contamination.
Document the clearance process and any findings for record-keeping purposes.
Ensure pro...
BPR/BCR/ECR are review points in business process management.
BPR stands for Business Process Reengineering, involves radical redesign of processes for improvement.
BCR stands for Business Continuity Review, ensures processes are in place to maintain operations during disruptions.
ECR stands for Engineering Change Review, evaluates proposed changes to products or processes for impact.
Review points help ensure efficiency,
posted on 30 Oct 2024
I applied via Walk-in and was interviewed in Sep 2024. There was 1 interview round.
My daily activities as an In-Process Quality Assurance (IPQA) officer involve monitoring and ensuring quality standards are met during production.
Conducting in-process inspections to verify product quality
Reviewing production documentation for accuracy and compliance
Identifying and addressing any quality issues or deviations
Collaborating with production team to implement corrective actions
Maintaining records of inspect
posted on 27 Jun 2024
I applied via Company Website and was interviewed in May 2024. There was 1 interview round.
posted on 11 Feb 2024
I applied via Approached by Company and was interviewed in Aug 2023. There were 3 interview rounds.
Change control is a process used to manage and document changes to a system or process.
Change control ensures that changes are properly reviewed, approved, and implemented.
It helps to minimize risks and ensure that changes do not negatively impact the quality or functionality of the system.
Change control typically involves documenting the change request, assessing its impact, obtaining necessary approvals, implementing...
Process validation is the process of establishing documented evidence that a process consistently produces a product meeting predetermined specifications.
There are three types of process validation: prospective validation, concurrent validation, and retrospective validation.
Prospective validation is conducted before the process is put into routine use.
Concurrent validation is performed during routine production.
Retrosp...
Audit trail is maintained by documenting and tracking all activities and changes made to a system or process.
Audit trail is created by recording all actions, events, and transactions that occur within a system.
It helps in ensuring accountability, traceability, and compliance with regulations.
Audit trail can be established through the use of logs, timestamps, and version control.
It is important to capture relevant infor...
Yes, I am interested in Microbiology analytical review.
I have a strong background in microbiology and enjoy analyzing data in this field.
I have experience conducting microbiological tests and interpreting the results.
I am familiar with various microbiological techniques and methodologies.
I am interested in staying updated with the latest advancements in microbiology research.
I believe that my knowledge and skills in mi...
Purified water specification refers to the set of requirements and standards that purified water must meet.
Purified water should have a low level of impurities, such as minerals, chemicals, and microorganisms.
It should meet the specifications outlined by regulatory bodies, such as the United States Pharmacopeia (USP) or European Pharmacopoeia (EP).
The pH level of purified water should be within a specific range, typica...
The purified water specification for microbial quality assurance.
Microbial specification for purified water is crucial to ensure its safety and suitability for use.
The specification typically includes limits for various microorganisms, such as bacteria, fungi, and endotoxins.
Commonly used tests for microbial quality assessment include total viable count, microbial identification, and endotoxin testing.
The specification...
Validation is the process of evaluating a system or component during or at the end of the development process to determine whether it satisfies specified requirements.
Functional Validation: Ensuring that the system meets the functional requirements.
Performance Validation: Verifying that the system performs as expected under different load conditions.
Security Validation: Checking the system for vulnerabilities and ensur...
posted on 5 Oct 2023
I applied via Approached by Company and was interviewed before Oct 2022. There were 3 interview rounds.
posted on 15 Sep 2022
I applied via Campus Placement and was interviewed before Sep 2021. There was 1 interview round.
I applied via Walk-in and was interviewed in Aug 2024. There was 1 interview round.
PCR stands for Polymerase Chain Reaction, a technique used in molecular biology to amplify a single or a few copies of a piece of DNA.
PCR is a common technique used in molecular biology to make multiple copies of a specific DNA segment.
It involves a series of temperature changes to denature, anneal, and extend DNA strands.
PCR is used in various applications such as DNA sequencing, gene cloning, and genetic testing.
Exam...
Buffer preparation involves mixing a weak acid and its conjugate base to maintain a stable pH.
Dissolve the weak acid in water
Add the conjugate base to the solution
Adjust the pH as needed with a strong acid or base
Use a pH meter to ensure the desired pH is achieved
Common buffers include phosphate buffer, acetate buffer, and Tris buffer
I applied via Walk-in and was interviewed in Dec 2023. There was 1 interview round.
Reviews of PVR and PQRS can be conducted through a systematic process involving data analysis and evaluation.
Collect and analyze data related to PVR and PQRS
Evaluate the performance and quality based on established criteria
Identify areas of improvement and develop action plans
Implement changes and monitor the impact
Continuously review and update the process to ensure ongoing quality assurance
posted on 1 Sep 2022
Antiviral drugs, Company products
posted on 9 Apr 2022
I applied via Referral and was interviewed in Mar 2022. There was 1 interview round.
based on 6 reviews
Rating in categories
Officer
494
salaries
| ₹1.8 L/yr - ₹5.9 L/yr |
Senior Officer
302
salaries
| ₹2.8 L/yr - ₹7.2 L/yr |
Executive
209
salaries
| ₹3.7 L/yr - ₹9.6 L/yr |
Research Associate
156
salaries
| ₹2.4 L/yr - ₹5.2 L/yr |
Production Officer
147
salaries
| ₹1.8 L/yr - ₹5.9 L/yr |
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