Aurobindo Pharma Interview Questions and Answers

Q1. Asked regarding quality control tests for tablets and capsules?
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Q2. Disintegration and dissolution
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Q1. Introduction on myself.
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Q2. Work experience
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Group discussion for pm and rm cheak it

Q1. How did you work in printing packaging experience
Ans. 
I have 5 years of experience working in printing packaging, managing vendor relationships and ensuring timely delivery of materials.
• Managed vendor relationships to negotiate pricing and ensure quality standards were met

• Coordinated with production team to meet deadlines and maintain inventory levels

• Implemented cost-saving measures by optimizing packaging designs

• Utilized ERP systems to track orders and manage inventory

• Re...read more
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Q2. How did you work in pharma industry ex4
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I have extensive experience working in the pharma industry, specifically in procurement and sourcing.
• Managed supplier relationships to ensure timely delivery of pharmaceutical products

• Negotiated contracts with vendors to secure competitive pricing

• Implemented cost-saving strategies while maintaining quality standards

• Stayed updated on industry trends and regulations to make informed purchasing decisions
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Q1. What action you take when Media Fail ?
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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
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Q2. Difference between API, BULK, and Formulation ?
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Q3. Why always c letter small in cGMP Guidelines ?
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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.
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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 ...read more
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Q1. Brief regarding aseptic practice?
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Q2. What is your goals about your professional groth?
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Q3. Explane the hyoploan glves intergity
Ans. 
Hypalon gloves provide integrity by offering high chemical resistance, durability, and protection against cuts and punctures.
• Hypalon gloves are made from a synthetic rubber material known for its resistance to chemicals, oils, and extreme temperatures.

• They are durable and provide excellent protection against cuts, punctures, and abrasions.

• These gloves maintain their integrity even in harsh working environments, making ...read more
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Q4. As an AI language model, my primary goal is to provide accurate and helpful information to assist users with their questions and tasks. My development focuses on improving natural language understanding, c...read more
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Q5. Aseptic practice refers to a set of techniques and procedures designed to prevent the contamination of sterile environments, surfaces, or substances. It's crucial in healthcare settings, pharmaceutical man...read more
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Q6. Sure, feel free to ask!
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Q7. What would you like to know?
Ans. 
I would like to know about the team's current projects, challenges, and opportunities for growth within the role.
• What are the key projects the team is currently working on?

• What challenges does the team face that I could help address?

• Are there opportunities for professional development and training?

• How does the team measure success and performance?

• What tools and technologies are being used in the projects?
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Q1. What is the Wruster principle?
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The Wruster principle is a concept in fluid dynamics that explains the behavior of fluid flow around a moving object.
• The Wruster principle states that when a fluid flows around a moving object, the pressure on the front side of the object decreases, causing the fluid to accelerate and create a low-pressure zone.

• This low-pressure zone then pulls the object forward, creating thrust in the direction of the fluid flow.

• The ...read more
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Q2. What is the combination of a wruster plate?
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A wruster plate is a combination of a thruster and a rudder plate used in marine propulsion systems.
• A wruster plate combines the functions of a thruster (for lateral movement) and a rudder plate (for steering).

• It is commonly used in marine propulsion systems to improve maneuverability.

• The wruster plate allows for more precise control and easier handling of large vessels in tight spaces.
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Q3. Which product you are handle?
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I handle a variety of electronic products, including smartphones, laptops, and tablets.
• Smartphones

• Laptops

• Tablets
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Q4. How many types off pellet coating?
Ans. 
There are several types of pellet coating used in various industries.
• Sugar coating

• Film coating

• Enteric coating

• Controlled release coating

• Functional coating
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Q5. What is data integrity
Ans. 
Data integrity refers to the accuracy, consistency, and reliability of data throughout its lifecycle.
• Ensuring data is accurate and consistent

• Preventing unauthorized access or modifications

• Implementing data validation processes

• Regularly backing up data to prevent loss

• Examples: checksums, encryption, access controls
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Q1. Anyone question
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Q2. CVC coating and fbd
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Q3. Pmp and meantenance
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Q4. Compression Blander
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Q5. Shifter and comail and. OCG
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Q6. LTD LPD
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Q1. Key role of apqr and how handling of stabilities
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Q2. Production plan of monitoring of QC Everything is key role if prices
Ans. 
Effective QC monitoring is crucial for maintaining production quality and controlling costs.
• Establish clear QC metrics to assess product quality, such as defect rates and compliance with specifications.

• Implement regular audits and inspections to ensure adherence to QC standards, e.g., weekly checks on production lines.

• Utilize statistical process control (SPC) to monitor production processes in real-time, allowing for i...read more
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Q3. Audits levrl change control s documentation and deviation and profuct recalls
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Q4. Reworking and reprocessing
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