Amneal Pharmaceuticals Assistant Manager Interview Questions, Process, and Tips

Q1. Introduce your self
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Q2. Describe your job role
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Q1. Introduce your self
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Q2. Decribe your self?
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Q3. How to develop RS method on HPLC?
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To develop RS method on HPLC, one must consider factors like column selection, mobile phase composition, and detection wavelength.
• Select an appropriate column based on the properties of the analytes being separated.

• Optimize the mobile phase composition to achieve good resolution and peak shape.

• Choose the appropriate detection wavelength for optimal sensitivity and selectivity.

• Validate the method by testing for linearit...read more
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Q4. HOW TO DO VALIDATION?, WHICH GUIDE LINE YOU FOLLOW?
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Validation is done by following guidelines and standards to ensure accuracy and reliability of data.
• Follow industry standards and best practices for validation

• Use validation tools and software to automate the process

• Perform manual checks and reviews to ensure data accuracy

• Document validation procedures and results for future reference

• Regularly update validation processes to adapt to changing requirements
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Q5. WHAT IS MACO value?, how to calculate?
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MACO value is the Minimum Acceptable Compliance Objective, used to determine the minimum level of compliance required in a system.
• MACO value is calculated based on the specific requirements and regulations of the system or industry.

• It is typically determined by assessing the potential risks and consequences of non-compliance.

• MACO value helps set a baseline for acceptable compliance levels and guides decision-making pro...read more
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Q6. What kind of instruments you have handled?
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I have handled a variety of instruments including cash registers, computer software, and office equipment.
• Cash registers

• Computer software

• Office equipment
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Q7. Are you aware about LIMS, ALCOA+, working in GMP envioronment?
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Yes, I am aware of LIMS, ALCOA+, and working in a GMP environment.
• LIMS stands for Laboratory Information Management System, used for managing laboratory data and workflows.

• ALCOA+ principles ensure data integrity in regulated environments, including GMP.

• Working in a GMP environment involves following strict guidelines to ensure product quality and safety.

• For example, in a pharmaceutical company, adherence to GMP ensures...read more
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Q8. How many people reporting to you?.
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Q9. How can you handle the work pressure?
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Q10. Have you done dissolution development?
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Q1. Introduce your self?
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Q2. Describe your job profile?
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Q3. What you have to become in next five years?
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Q4. What is zeta potential?
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Zeta potential is the electrical charge at the slipping plane of a particle in a dispersion.
• Zeta potential is a key parameter in colloidal systems, influencing stability and interactions between particles.

• It is measured in millivolts (mV) and can be positive, negative, or zero.

• Higher zeta potential values indicate greater repulsion between particles, leading to increased stability.

• For example, in pharmaceuticals, zeta ...read more
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Q5. How can you determine this technique is best one?
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The best technique can be determined by evaluating its effectiveness, efficiency, feasibility, and alignment with goals.
• Assess the success rate of the technique in achieving desired outcomes.

• Consider the cost and resources required to implement the technique.

• Evaluate the practicality and ease of implementation of the technique.

• Ensure that the technique aligns with the overall goals and objectives of the organization.

• Se...read more
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Q1. Why would you like join our organisation?
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Q2. Your expected CTC?
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Q3. Are you ready to relocate?
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Q1. About method development of peptide
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Q2. Not answered since I didn't do
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Q1. General technical knowledge and awareness of pharma portfolio management
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Evaluation of NDA, patents, competitive mapping, and designing 505b(2) strategy

Q1. One on one round about general pharmaceutical field and presentation of assignment
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