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Macleods Pharmaceuticals Senior Executive QC Interview Questions and Answers
Macleods Pharmaceuticals Senior Executive QC Interview Experiences
1 interview found
I applied via Walk-in and was interviewed before Oct 2021. There were 2 interview rounds.
(2 Questions)
- Q1. Instrument operation and calibration based questions
- Q2. Method validation for Assay by HPLC
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Senior Executive QC Interview Questions & Answers
Intas Pharmaceuticals
Raju Bhaskar Netake
posted on 14 Aug 2024
Selected
I applied via Walk-in and was interviewed in Feb 2024. There were 2 interview rounds.
(10 Questions)
- Q1. How many ICH guidelines?, and it's topics
- Q2. Dissolution criteria for extended release drug
- Q3. ALCOA++ related questions
- Q4. Type of Audit trail?
- Ans.
Audit trails are logs that track changes made to data, providing a record of who made the changes, when, and why.
Audit trails are essential for maintaining data integrity and compliance with regulations.
They help in identifying errors, fraud, or unauthorized access to data.
Examples of audit trails include logs of user actions in a software system, changes made to a document, or modifications to a database.
Audit trails ...
- Q5. What is the formula for calculating CU value or for AV
- Ans.
The formula for calculating CU value or AV is based on the number of defects found during quality control inspections.
CU value (Criticality Unit) is calculated by assigning a weight to each type of defect based on its impact on the product or process.
AV (Acceptance Value) is calculated by summing up the CU values of all defects found during inspections.
Formula: AV = Σ(CU value of all defects)
Example: If a product has 3...
- Q6. What are the check points for dissolution test?
- Ans.
Check points for dissolution test include equipment calibration, sample preparation, media selection, temperature control, and data analysis.
Calibrate equipment regularly to ensure accurate results
Properly prepare samples to ensure consistency
Select appropriate media for dissolution based on drug solubility
Maintain proper temperature control throughout the test
Analyze data accurately to determine dissolution rate
- Q7. What is UCL and LCL? And how they calculated?
- Ans.
UCL and LCL stand for Upper Control Limit and Lower Control Limit, respectively. They are statistical measures used in quality control to determine if a process is stable and in control.
UCL is the highest value that a process can reach before it is considered out of control.
LCL is the lowest value that a process can reach before it is considered out of control.
UCL and LCL are typically calculated using statistical meth...
- Q8. If any extraneous peak observe in GC analysis, then how can you handle that?
- Ans.
Extraneous peaks in GC analysis can be handled by identifying the source of contamination, adjusting parameters, and re-analyzing the sample.
Identify the source of contamination by checking sample preparation, column condition, or instrument cleanliness.
Adjust parameters such as temperature, flow rate, or injection volume to minimize extraneous peaks.
Re-analyze the sample after making necessary adjustments to ensure ac...
- Q9. Which are the stability zones, and thier conditions?
- Q10. How to handle NQI and QI or decesion power to take incident or not?
- Ans.
Handling NQI and QI incidents requires thorough evaluation and decision-making based on established protocols.
Thoroughly investigate the incident to determine if it falls under NQI (Non-Quality Incident) or QI (Quality Incident).
Refer to established guidelines, protocols, and quality standards to assess the severity and impact of the incident.
Consider the potential risks to patient safety, regulatory compliance, and ov...
(2 Questions)
- Q1. Why are you left your current organisation?
- Ans.
Seeking new challenges and opportunities for growth.
Desire for new challenges and opportunities for professional growth
Looking for a more supportive work environment
Seeking better work-life balance
Company restructuring or downsizing
Relocation to a different city or country
- Q2. How much rise you want?
- Ans.
I am open to discussing a rise based on my qualifications, experience, and the responsibilities of the role.
I am looking for a competitive salary that reflects my skills and experience.
I am open to negotiation based on the responsibilities and expectations of the role.
I would like to discuss the potential for performance-based bonuses or incentives.
I am interested in opportunities for career growth and development with
Interview Preparation Tips
Quality Control Officer Interview Questions & Answers
Ajanta Pharma
Farazahmad Nazirmahmad Rana
posted on 9 Aug 2024
Selected
I applied via Walk-in and was interviewed in Feb 2024. There were 2 interview rounds.
(2 Questions)
- Q1. Explain data integrity in pharma industry
- Q2. Explain oos and incident
- Ans.
OOS stands for Out of Specification and refers to test results that fall outside the acceptable range. Incidents are unexpected events that may impact product quality.
OOS results indicate a deviation from the specified requirements or standards.
Incidents are unexpected events that may impact product quality or safety.
OOS results may require investigation to determine the root cause and corrective actions.
Examples of in...
(2 Questions)
- Q1. What is data integrity
- Ans.
Data integrity refers to the accuracy, consistency, and reliability of data throughout its lifecycle.
Ensuring data is accurate and reliable
Preventing unauthorized access or modifications
Maintaining consistency and completeness of data
Implementing security measures to protect data integrity
- Q2. Family background why you shifting job
- Ans.
I am shifting jobs to pursue better career growth opportunities and to utilize my skills and experience in a new environment.
Seeking better career growth opportunities
Utilizing skills and experience in a new environment
Exploring new challenges and responsibilities
Skills evaluated in this interview
It is extremely tough and hard
(2 Questions)
- Q1. What is sop stands for
- Ans.
SOP stands for Standard Operating Procedure.
SOP is a set of step-by-step instructions compiled by an organization to help workers carry out routine operations.
It ensures consistency and quality in the performance of tasks.
Examples include SOPs for laboratory testing procedures, manufacturing processes, and safety protocols.
- Q2. What is GMP stands for
- Ans.
GMP stands for Good Manufacturing Practice.
GMP is a set of guidelines that ensure products are consistently produced and controlled according to quality standards.
It is important in industries such as pharmaceuticals, food, and cosmetics.
Examples of GMP requirements include proper documentation, sanitation, and quality control measures.
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Avijit Das
I applied via LinkedIn and was interviewed before Nov 2023. There were 3 interview rounds.
G O O D I N T E R V I E W
(2 Questions)
- Q1. WHY YOU JOIN QC
- Q2. WHAT IS STRENGTH AND WEAKNESS
(2 Questions)
- Q1. WHAT IS QC OR QA
- Ans.
QC (Quality Control) and QA (Quality Assurance) are processes used to ensure products meet quality standards.
QC involves testing and inspecting products to ensure they meet specific quality standards.
QA focuses on creating processes and procedures to prevent defects in products.
QC is reactive, while QA is proactive.
Examples: QC involves testing the purity of chemicals in a lab, while QA involves implementing SOPs to pr
- Q2. HPLC GC GAS CHROMATOGRAPHY
Selected
I applied via Walk-in and was interviewed in Sep 2023. There were 2 interview rounds.
(4 Questions)
- Q1. Self introduction
- Q2. Basic Subject Related
- Q3. Biochemistry and Inorganic Chemistry
- Q4. Salary package and Group discuss
Interview Preparation Tips
- Biochemistry
Selected
I applied via Campus Placement and was interviewed in Dec 2023. There were 2 interview rounds.
Range problem so i cant give to this aptitude test
(1 Question)
- Q1. All about Qc HPLC Gas C
Interview Preparation Tips
Selected
I applied via Referral and was interviewed before Jan 2023. There was 1 interview round.
(1 Question)
- Q1. About related microbiology , Environmental monitoring in specific areas and levels, water sampling.
QC Officer Interview Questions & Answers
Finecure Pharmaceuticals
Garima Bisht
posted on 22 May 2022
I applied via Naukri.com and was interviewed before May 2021. There were 3 interview rounds.
(2 Questions)
- Q1. General Introduction
- Q2. Discussion About study of pharma and subjects
(2 Questions)
- Q1. Basic of pharma and industrial training and experience
- Q2. General of pharmacutical and tablet dosage form
Interview Preparation Tips
Senior Executive QC Interview Questions & Answers
Intas Pharmaceuticals
Suraj Singh
posted on 11 Feb 2024
Selected
I applied via Referral and was interviewed before Feb 2023. There were 4 interview rounds.
(2 Questions)
- Q1. HR generally start with introduction than ask about your current profile as per their requirements and achievements
- Q2. Why candidates wants to change the organisation
(2 Questions)
- Q1. Interviewer always ask for Wht is your current profile based upon that question frequently ask by interviewer
- Q2. Calibration Guidelines Investigation tools
(2 Questions)
- Q1. Technical ability of candidate
- Q2. Communication, behaviour, Achivements
(2 Questions)
- Q1. Salary discussion, Notice period negotiation
- Q2. Joining date and onboards and company policy discussion
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Macleods Pharmaceuticals Senior Executive QC Reviews and Ratings
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| ₹2.8 L/yr - ₹8.7 L/yr |
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| ₹1.9 L/yr - ₹4.2 L/yr |
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