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10+ NorthStar Ship Management Interview Questions and Answers

Updated 8 Aug 2024

Q1. why are kept in stability samples

Ans.

Stability samples are kept to ensure the quality and efficacy of a product over time.

  • To monitor the degradation of the product over time

  • To determine the shelf life of the product

  • To ensure the product remains safe and effective for use

  • To comply with regulatory requirements

  • Examples: pharmaceuticals, cosmetics, food products

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Q2. different between ws standards $ Rs standards

Ans.

WS standards are for web services while RS standards are for remote procedure calls.

  • WS standards are used for communication between different systems over the internet.

  • RS standards are used for communication between processes on the same system.

  • WS standards include SOAP, WSDL, and UDDI.

  • RS standards include CORBA, DCOM, and Java RMI.

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Q3. What are acids bases

Ans.

Acids and bases are two types of chemical substances with opposite properties.

  • Acids have a pH less than 7, while bases have a pH greater than 7.

  • Acids are sour in taste, while bases are bitter in taste.

  • Acids react with metals to produce hydrogen gas, while bases react with acids to produce salt and water.

  • Examples of acids include vinegar, lemon juice, and battery acid, while examples of bases include soap, bleach, and baking soda.

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Q4. Have you work on iso documentation

Ans.

Yes, I have experience working on ISO documentation.

  • I have worked on developing and implementing ISO 14001 Environmental Management System documentation.

  • I have experience in maintaining ISO 45001 Occupational Health and Safety Management System documentation.

  • I have conducted internal audits to ensure compliance with ISO standards.

  • I have updated ISO documentation based on changes in regulations or company policies.

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Q5. What is safety, what is risky, what is the accident

Ans.

Safety is the state of being protected from harm, risk is the likelihood of harm occurring, and an accident is an unexpected event resulting in harm.

  • Safety involves taking measures to prevent harm from occurring

  • Risk is the probability of harm occurring, and can be reduced through safety measures

  • An accident is an unexpected event that results in harm, and can be caused by unsafe conditions or behaviors

  • Examples of safety measures include wearing personal protective equipment, f...read more

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Q6. What is the lifecycle of data

Ans.

The lifecycle of data refers to the stages of data from its creation to its disposal.

  • Data creation

  • Data storage

  • Data processing and analysis

  • Data sharing and dissemination

  • Data archiving and disposal

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Q7. Your experience on audit handling briefly

Ans.

Handled audits by conducting thorough inspections, documenting findings, and implementing corrective actions.

  • Conducted regular audits to ensure compliance with EHS regulations

  • Documented audit findings and communicated them to relevant stakeholders

  • Implemented corrective actions to address any non-compliance issues

  • Maintained audit records for future reference

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Q8. Explain the definition of ph

Ans.

pH is a measure of the acidity or basicity of a solution.

  • pH stands for 'potential of hydrogen'.

  • It is measured on a scale of 0-14, with 7 being neutral.

  • Solutions with a pH less than 7 are acidic, while those with a pH greater than 7 are basic.

  • The pH of a solution can be determined using a pH meter or pH paper.

  • Examples of pH values: lemon juice (pH 2), milk (pH 6.5), baking soda (pH 9).

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Q9. Explain the normality

Ans.

Normality refers to the concentration of a solution in terms of the number of equivalents of solute per liter of solution.

  • Normality is a measure of concentration used in acid-base reactions.

  • It is defined as the number of equivalents of solute per liter of solution.

  • For example, a 1N solution of HCl contains 1 mole of H+ ions per liter of solution.

  • Normality is different from molarity, which is a measure of concentration based on the number of moles of solute per liter of soluti...read more

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Q10. What is batch procedure

Ans.

Batch procedure is a method of processing data or tasks in groups or batches rather than individually.

  • Batch procedure involves grouping similar tasks together to be executed at the same time.

  • It helps in optimizing resources and improving efficiency by reducing processing time.

  • Examples include batch processing in computer systems, where multiple jobs are executed together, and batch production in manufacturing, where products are made in batches.

  • Batch procedures are commonly u...read more

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Q11. Explain the molarity

Ans.

Molarity is a measure of the concentration of a solution in terms of the number of moles of solute per liter of solution.

  • Molarity is expressed in units of moles per liter (mol/L or M)

  • It is calculated by dividing the number of moles of solute by the volume of the solution in liters

  • For example, a solution containing 0.5 moles of solute in 1 liter of solution has a molarity of 0.5 M

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Q12. What is GMP and cGMP

Ans.

GMP stands for Good Manufacturing Practices and cGMP stands for current Good Manufacturing Practices.

  • GMP is a set of guidelines that ensure products are consistently produced and controlled according to quality standards.

  • cGMP is an updated version of GMP that incorporates current best practices and technologies.

  • Both GMP and cGMP are crucial in industries like pharmaceuticals, food, and cosmetics to ensure product safety and quality.

  • Examples of GMP/cGMP requirements include pr...read more

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Q13. What is validation

Ans.

Validation is the process of ensuring that a product, service, or system meets the requirements and specifications set forth.

  • Validation involves checking if the product meets the customer's requirements.

  • It ensures that the product is fit for its intended use.

  • Validation can include testing, inspection, and review processes.

  • Examples of validation include software testing to ensure it functions correctly and validation of medical devices to ensure they are safe and effective.

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