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10+ Orangebits Software Technologies Interview Questions and Answers

Updated 19 Dec 2024

Q1. What are the differences between working in a FMCG (Fast-Moving Consumer Goods) manufacturing department and in other manufacturing companies?

Ans.

FMCG manufacturing departments focus on high volume production of consumer goods with short shelf life, while other manufacturing companies may have different production processes and target markets.

  • FMCG manufacturing departments prioritize efficiency and speed due to the perishable nature of the products.

  • Other manufacturing companies may focus on quality control and customization of products.

  • FMCG companies often have strict regulations and standards to meet due to the nature...read more

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Q2. What are some key bullet points outlining the manufacturing procedures of products in which you have experience?

Ans.

Key bullet points outlining manufacturing procedures of products

  • Implementing lean manufacturing principles to optimize production processes

  • Utilizing Six Sigma methodologies to improve quality and reduce defects

  • Ensuring compliance with industry regulations and standards such as ISO 9001

  • Implementing continuous improvement initiatives to enhance efficiency and productivity

  • Utilizing advanced manufacturing technologies such as robotics and automation

  • Collaborating with cross-functi...read more

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Q3. What are the Critical Control Points (CCPs) that should be followed in the manufacturing section?

Ans.

Critical Control Points (CCPs) are specific points in the manufacturing process where control measures can be applied to prevent, eliminate, or reduce hazards.

  • Identify potential hazards in the manufacturing process

  • Establish critical limits for each CCP

  • Monitor CCPs to ensure they are within critical limits

  • Implement corrective actions if a deviation occurs

  • Verify the effectiveness of the CCPs through regular testing and validation

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Q4. What is your understanding of ISO 14001 and Environmental Management Systems (EMS)?

Ans.

ISO 14001 is a standard for Environmental Management Systems (EMS) that helps organizations minimize their environmental impact.

  • ISO 14001 sets out the criteria for an environmental management system that a company can follow to improve their environmental performance.

  • EMS helps organizations identify, manage, monitor, and control their environmental issues in a systematic way.

  • It involves establishing policies, setting objectives, implementing processes to achieve those objecti...read more

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Q5. What do you know about validation and qualification, and what are their different types?

Ans.

Validation and qualification are important processes in manufacturing to ensure products meet quality standards.

  • Validation is the process of establishing documented evidence that a system or process consistently produces a result meeting predetermined specifications.

  • Qualification is the process of demonstrating that equipment or systems are suitable for their intended use.

  • Types of validation include process validation, cleaning validation, and analytical method validation.

  • Typ...read more

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Q6. What is your understanding of Current Good Manufacturing Practices (cGMP)?

Ans.

cGMP are regulations ensuring quality, safety, and consistency in manufacturing processes.

  • cGMP are regulations set by the FDA to ensure quality, safety, and consistency in the manufacturing of pharmaceuticals, food, and other products.

  • They cover areas such as facility design, equipment maintenance, personnel training, record-keeping, and product testing.

  • Adherence to cGMP helps prevent contamination, mix-ups, and errors in the manufacturing process.

  • Examples of cGMP requirement...read more

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Q7. What do you know about GDP and ALCOA or ALCOA++?

Ans.

GDP stands for Gross Domestic Product, while ALCOA or ALCOA++ are quality management systems used in manufacturing.

  • GDP is a measure of a country's economic performance, representing the total value of all goods and services produced over a specific time period.

  • ALCOA is a quality management system focusing on ensuring data integrity in pharmaceutical manufacturing.

  • ALCOA++ expands on ALCOA by adding attributes like Complete, Consistent, Enduring, and Available to ensure data re...read more

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Q8. What is a Quality Management System (QMS)?

Ans.

A QMS is a set of policies, processes, and procedures required for planning and execution in the core business area of an organization.

  • QMS helps ensure products meet customer requirements and comply with regulations

  • It involves quality planning, control, assurance, and improvement

  • Examples of QMS include ISO 9001 certification and Six Sigma methodologies

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Q9. What is your understanding of ISO 22715?

Ans.

ISO 22715 is a standard that specifies requirements for packaging and labeling of cosmetic products.

  • ISO 22715 sets guidelines for the packaging and labeling of cosmetic products to ensure consumer safety and product quality.

  • It covers aspects such as labeling requirements, packaging materials, and information that must be included on the product packaging.

  • Compliance with ISO 22715 helps cosmetic manufacturers meet regulatory requirements and maintain consistency in product pre...read more

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Q10. What are Six Sigma, 5S, and HIRA?

Ans.

Six Sigma, 5S, and HIRA are methodologies used in manufacturing for process improvement, workplace organization, and risk assessment.

  • Six Sigma is a data-driven methodology aimed at reducing defects and improving quality in processes.

  • 5S is a workplace organization method focusing on Sort, Set in order, Shine, Standardize, and Sustain.

  • HIRA stands for Hazard Identification and Risk Assessment, used to identify and mitigate potential risks in manufacturing processes.

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