AstraZeneca Assistant Manager Interview Questions and Answers

Q1. About your experience
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Q1. Process Validation related.
Ans. Description of process validation and impact
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Q2. CPP parameters description and impact on which CQA
Ans. 
CPP parameters refer to Critical Process Parameters which have a significant impact on Critical Quality Attributes (CQA) in manufacturing processes.
• CPP parameters are specific process variables that must be controlled within a certain range to ensure product quality.

• Examples of CPP parameters include temperature, pressure, flow rate, and mixing speed.

• The impact of CPP parameters on CQA can be seen in the final product ...read more
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Q3. Stability studies for pharmaceutical products.
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Q4. Annual report submission procedure for usfda approved products.
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The annual report submission procedure for USFDA approved products involves compiling data on product performance, safety, and compliance with regulations.
• Compile data on product performance, safety, and compliance with USFDA regulations

• Submit the annual report to the USFDA within the specified deadline

• Include information on any changes in manufacturing processes or product labeling

• Ensure all data submitted is accurate...read more
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Q1. Reason for leaving the job
Ans. For better opportunity and diversity in my career.
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Does global warming leads the world into destruction or Scientists will find out ways and means to face this issue,?

Sudden fall of sales of a high demand product because of an article published in a world famous medical journal Lancet (example)

Q1. Sap T code
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Q2. What are your experiences with customer handling? I have 12 years Customer handling
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Q3. Logistics department
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Q4. Logistics department handling to deliver time to time with customer satisfaction.
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Q5. MIS Data handling and reporting
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Q1. What is qualification of m/c in packing. Tell me flow process, which way u did qualification in your previous company.
Ans. 
Qualification of machine in packing and flow process
• Qualification of machine in packing involves testing and validating the machine's performance and capabilities

• Flow process includes steps like installation, operational testing, performance testing, and documentation

• In my previous company, we followed a qualification protocol that included IQ, OQ, and PQ stages

• We also conducted periodic requalification to ensure the m...read more
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Q2. What is OEE, SHIFT WISE SHOW ME OEE CALCULATIONS.
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OEE (Overall Equipment Effectiveness) measures manufacturing productivity by evaluating availability, performance, and quality.
• OEE = Availability x Performance x Quality.

• Availability = (Operating Time / Planned Production Time) x 100%.

• Performance = (Actual Output / Ideal Output) x 100%.

• Quality = (Good Output / Total Output) x 100%.

• Example: If a machine runs for 8 hours (480 minutes) but is down for 1 hour, availability...read more
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Q1. How r u doing the change part validation & its process. What is action plan if leak test failed in blisters.
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Q1. Why u want to leave the company. What is your CTC & etc.
Ans. 
I seek new challenges and growth opportunities that align with my career goals and aspirations.
• Desire for professional growth: I feel that I have reached a plateau in my current role and am eager to take on new challenges.

• Alignment with career goals: The new position aligns better with my long-term career aspirations in management.

• Company culture: I am looking for a work environment that fosters innovation and collabor...read more
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Q1. Regarding my PhD work and industrial work
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Q1. Sallery and relocation
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