RPG Life Sciences Product Management Trainee Interview Questions and Answers

Q1. Related to experience
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Q1. Package discussion and position
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Q1. About the job knowledge
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Q2. How we are suitable for position
Ans. 
I have extensive experience in leadership roles and a proven track record of successfully managing teams and achieving targets.
• Strong leadership skills demonstrated through previous roles

• Proven track record of meeting and exceeding targets

• Excellent communication and interpersonal skills

• Ability to motivate and inspire team members

• Experience in strategic planning and decision-making
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Q3. How you manage the team
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Q4. How many audits you faced
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I have faced audits in my previous role as a Deputy Manager.
• I have faced audits from both internal and external auditors.

• I have experience in preparing for audits, gathering necessary documentation, and participating in audit meetings.

• I have successfully addressed audit findings and implemented corrective actions to improve processes.

• I have been involved in audits related to financial records, compliance with regulatio
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Q5. What recent audit observations
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I recently observed discrepancies in inventory management during an audit.
• Identified inconsistencies in inventory records vs physical count

• Noted lack of proper documentation for inventory transactions

• Discovered expired or damaged inventory items not properly accounted for
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Handling of equipment manpower handling product process

Q1. Analytical mechanical
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Q2. Product process improvement yeild
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Q1. Problem solving skills,
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Q2. Leadership qualities, techical skills, subject knowledge
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Q1. Explain about cleaning validation
Ans. 
Cleaning validation is the process of ensuring that cleaning procedures effectively remove residues from equipment to prevent cross-contamination.
• Cleaning validation is essential in industries like pharmaceuticals, food production, and cosmetics to ensure product quality and safety.

• It involves establishing cleaning procedures, setting acceptance criteria, and conducting tests to verify cleanliness.

• Analytical techniques...read more
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Q2. Explain about maco calculation
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MACO calculation is used to determine the maximum allowable carryover of a substance in a cleaning process.
• MACO stands for Maximum Allowable Carryover

• It is calculated based on the acceptable daily intake (ADI) of the substance and the worst-case scenario for residue on equipment

• MACO calculation helps ensure that cleaning processes are effective in removing residues to prevent cross-contamination

• Example: If the ADI of a...read more
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Q3. Explain about gmp
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GMP stands for Good Manufacturing Practices, which are guidelines and regulations set by regulatory agencies to ensure the quality and safety of products.
• GMP is a set of guidelines and regulations that ensure products are consistently produced and controlled according to quality standards.

• It covers all aspects of production, including the facilities, equipment, personnel, and processes.

• Examples of GMP requirements incl...read more
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Q4. Explain about heat load
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Heat load refers to the amount of heat energy that needs to be removed or added to a space to maintain a desired temperature.
• Heat load is calculated based on factors such as the size of the space, insulation, number of occupants, equipment, and climate conditions.

• Examples of heat load include solar heat gain through windows, heat generated by lighting and equipment, and heat loss through walls and roofs.

• Understanding h...read more
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Q5. What are all QMS tool used , ple explain briefly,and what are all documents mainten during production
Ans. 
Various QMS tools such as FMEA, Control Charts, and 5S are used in production. Documents maintained include SOPs, work instructions, and production logs.
• QMS tools used in production include Failure Mode and Effects Analysis (FMEA), Control Charts, and 5S methodology

• Documents maintained during production may include Standard Operating Procedures (SOPs), work instructions, production logs, and quality records

• FMEA is used...read more
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Q6. What is your achievements,u r involved any oos investigation if yes ple explain
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Q1. What was your work profile and did you have exposure to multiple locations
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Q2. What is your exposure to quality systems and CSV
Ans. 
I have extensive exposure to quality systems and CSV.
• I have implemented and maintained quality systems such as ISO 9001 and GMP.

• I have experience in Computer System Validation (CSV) for regulated industries.

• I have conducted CSV audits and ensured compliance with regulatory requirements.

• I have trained teams on quality systems and CSV best practices.

• I have worked with cross-functional teams to ensure quality and complian
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Q1. Which was the toughest task handled by you
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Q2. What you feel is unique achievement
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Q1. Experience in training technology implementation and compliance
Ans. 
I have extensive experience in implementing training technology and ensuring compliance.
• Developed and implemented training programs for new software systems at previous company

• Ensured compliance with industry regulations and company policies through regular audits and training sessions

• Collaborated with IT department to troubleshoot any technical issues during implementation

• Trained and coached team members on new techno
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Q1. Details of experience
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Q1. What is it you will do differently in your current company
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Q1. How will you upskill yourself
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