ACG Worldwide Assistant Manager Interview Questions and Answers

Q1. Regarding my PhD work and industrial work
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Q1. Sallery and relocation
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Q1. QMS related questions
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Q2. Compliance related questions
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Q1. CAPA flow and effectiveness check
Ans. 
CAPA flow involves identifying root causes, implementing corrective actions, and verifying effectiveness.
• CAPA stands for Corrective and Preventive Actions

• Flow involves identifying root cause, implementing corrective actions, and verifying effectiveness

• Root cause analysis is crucial in CAPA process

• Examples of CAPA effectiveness checks include trend analysis, audit findings, and customer complaints
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Q2. Root cause tools and Investigations flow.
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Q1. Risk assessment
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Q2. Change control, deviations, incidents and regulatory guidelines.
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Q1. Personal and General information
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Q2. Salary discussion
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Q1. Tell us about yourself
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Q2. What are the tools you use
Ans. 
I use a variety of tools such as project management software, communication tools, and data analysis tools to effectively manage tasks and teams.
• Project management software (e.g. Trello, Asana)

• Communication tools (e.g. Slack, Microsoft Teams)

• Data analysis tools (e.g. Excel, Google Analytics)
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Q1. Experience on job
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Q1. Can't offer fix d component
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Q1. Technical,Salary,Family and Relocation
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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.
Ans. 
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
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Q1. Reason for leaving the job
Ans. For better opportunity and diversity in my career.
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Q1. About salary only
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Q2. Position expectation and why to change
Ans. 
I have high expectations for the Assistant Manager position and am seeking a change to further develop my leadership skills and contribute to a dynamic team.
• Seeking new challenges and opportunities for growth

• Desire to take on more responsibilities and lead a team

• Passion for driving results and making a positive impact

• Looking to apply previous experience and skills in a new environment
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