Strides Pharma Asset Coordinator Interview Questions and Answers

Q1. Technical and Managerial skill
Add your answer

Through investigation case

Q1. About salary only
Add your answer
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
Answered by AI
Add your answer

Q1. About your self location environment
Add your answer

Q1. Type of Equipment Equipment cleaning contamination batch changing tipys of document data integrity ICH Q7 safety
Add your answer
Q2. Type of equipment cleaning
Ans. 
Equipment cleaning involves thorough disinfection and sterilization to prevent contamination.
• Use appropriate cleaning agents and disinfectants recommended for the specific equipment

• Follow manufacturer's instructions for cleaning and maintenance

• Regularly inspect equipment for any signs of wear or damage

• Implement proper storage practices to prevent contamination

• Train staff on proper cleaning procedures and protocols
Answered by AI
Add your answer
Q3. Batch charging process
Add your answer
Q4. Tipe of contamination
Ans. 
Contamination can be classified into three main types: chemical, biological, and physical.
• Chemical contamination involves the presence of harmful chemicals in a substance or environment.

• Biological contamination refers to the presence of harmful microorganisms such as bacteria, viruses, or fungi.

• Physical contamination occurs when foreign objects like glass, metal, or plastic are present in a substance.
Answered by AI
Add your answer

It's was based on vigilance

Q1. How do u manage ur work and life
Add your answer

Q1. Process Validation related.
Ans. Description of process validation and impact
Answered Anonymously
Add your answer
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
Answered by AI
View 1 more answer
Q3. Stability studies for pharmaceutical products.
Add your answer
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
Answered by AI
Add your answer

Q1. Reason for leaving the job
Ans. For better opportunity and diversity in my career.
Answered Anonymously
Add your answer

Q1. What is gmp and ngmp
Ans. 
GMP stands for Good Manufacturing Practice, which ensures products are consistently produced and controlled according to quality standards. NGMP is not a recognized term in this context.
• GMP is a set of guidelines for ensuring the quality and safety of products during manufacturing.

• GMP covers aspects such as personnel, premises, equipment, documentation, production, quality control, and more.

• Examples of industries that ...read more
Answered by AI
Add your answer
Q2. Solvent boiling point
Add your answer