Intas Pharmaceuticals Production Manager Interview Questions and Answers

Handling of trouble shooting, block maintain capabilities, processes related documents, and forms which are handled in manufacturing

Q1. Process related impurities,
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Q2. Safety precautions at manufacturing
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Safety precautions at manufacturing include proper training, use of personal protective equipment, regular equipment maintenance, and emergency response plans.
• Provide comprehensive safety training to all employees

• Ensure proper use of personal protective equipment (PPE)

• Regularly inspect and maintain equipment to prevent accidents

• Develop and implement emergency response plans for various scenarios
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Q3. Achievement at career
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Q1. What is your education and experience?
Ans. 
I have a Bachelor's degree in Industrial Engineering and 5 years of experience in production management.
• Bachelor's degree in Industrial Engineering

• 5 years of experience in production management
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Q2. What is your family background?
Ans. 
My family background is diverse and includes a mix of professions and cultural backgrounds.
• My parents come from different cultural backgrounds, enriching our family with diverse traditions and perspectives.

• Several members of my family work in various industries, including healthcare, education, and business.

• I have siblings who are pursuing careers in engineering and the arts, showcasing our range of interests and talen
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Q1. What is product changeover cleaning procedure?
Ans. 
Product changeover cleaning procedure involves thorough cleaning and sanitizing of equipment and work areas to prevent cross-contamination.
• Start by removing any remaining product from equipment and surfaces

• Use appropriate cleaning agents and sanitizers to clean all surfaces thoroughly

• Follow specific cleaning procedures outlined in the company's standard operating procedures (SOPs)

• Ensure all equipment is properly disass...read more
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Q2. What safety precautions to be taken while handling hazardous chemicals?
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Safety precautions include wearing appropriate personal protective equipment, proper ventilation, labeling containers, and storing chemicals properly.
• Always wear appropriate personal protective equipment such as gloves, goggles, and lab coats

• Ensure proper ventilation in the area where chemicals are being handled

• Label all containers with the name of the chemical and any hazard warnings

• Store chemicals in a secure locatio...read more
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Q1. What is production planning?
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Production planning is the process of organizing resources, scheduling tasks, and coordinating activities to ensure efficient and timely production of goods.
• Forecasting demand to determine production requirements

• Creating production schedules to optimize resources and meet deadlines

• Coordinating with suppliers to ensure timely delivery of materials

• Monitoring production processes to identify and address any issues

• Adjustin...read more
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Q2. What is clean room and it's classification?
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A clean room is a controlled environment with low levels of pollutants such as dust, airborne microbes, aerosol particles, and chemical vapors.
• Clean rooms are classified based on the number of particles allowed per cubic meter at a specified particle size.

• The classification is typically done according to international standards such as ISO 14644-1.

• Examples of clean room classifications include ISO Class 5, ISO Class 7,
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Q1. What is Granulation
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Granulation is a process in which small particles are formed by agglomerating powder particles.
• Granulation involves the binding of powder particles to form larger particles.

• It is commonly used in pharmaceutical manufacturing to improve flow properties and reduce dust.

• There are different methods of granulation such as wet granulation and dry granulation.
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Q2. Expalin 6M in deviation
Ans. 
6M in deviation refers to the factors that can cause a process to deviate from its intended outcome.
• 6M stands for Man, Machine, Material, Method, Measurement, and Mother Nature.

• These factors can contribute to variations in production processes.

• For example, a machine malfunction (Machine) can lead to deviations in product quality.

• Addressing each of the 6M factors can help minimize deviations and improve overall producti
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Q1. What is qualification
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Qualifications refer to the skills, knowledge, experience, or credentials required for a specific job or role.
• Qualifications can include educational degrees or certifications relevant to the field.

• Work experience in a similar role may also be a qualification.

• Specific skills such as technical abilities or language proficiency can be qualifications.

• Some positions may require specific licenses or accreditations.

• Soft skill...read more
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Q2. Degree B.com Cas
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Q3. What is technical qualification
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Technical qualification refers to the specific knowledge and skills required for a particular technical job or field.
• It includes formal education, certifications, training programs, and hands-on experience.

• Examples of technical qualifications include a degree in engineering, certification in project management, proficiency in programming languages, and experience with specific software or machinery.

• Technical qualificat...read more
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Q4. Tally prime in the withGST
Ans. 
Tally Prime is a software that includes GST features for managing production operations.
• Tally Prime is a popular accounting software used by businesses for managing various operations including production.

• It includes features for handling GST (Goods and Services Tax) calculations and compliance.

• With Tally Prime, production managers can easily track inventory, manage orders, and generate reports for decision-making.

• The ...read more
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Q5. What is your name.Tangi . Raghu
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Only some time in the. Finance in group dissection

Q1. Over all process
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Q2. About your personal skills
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Coordination well all concerns respectively

Using pharma and erp software

Maintain as per reviews, weekly and monthly training schedules

Assigned as per data and process as per cGMP

Investigate roote causes and made corrective and preventive actions

Q1. Well maintain with training schedules safety measures
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Q1. Ensures all activities and processes flow without failure of production as per planning
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Q1. Tecnical skills, gmp knowledge, guidelines.equipment and manpower handling.
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Q2. Team size and failure encountered.
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Q3. QMS knowledge and workflow for cc deviation in QMS software.
Ans. 
Understanding QMS knowledge and workflow for cc deviation in QMS software is essential for managing production processes effectively.
• QMS knowledge involves understanding quality management systems and their implementation in the production process.

• Workflow for cc deviation in QMS software includes identifying and documenting any deviations from the established quality control standards.

• Effective management of cc deviat...read more
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Q4. Qualification flow.
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Q5. Audit experience and exposure.
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