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10+ Synergy Maritime Interview Questions and Answers

Updated 4 Oct 2024

Q1. What is basic of spectroscopy, organic naming reactions with mechanism, hplc, ir, uv , mass spectroscopy, nmr spectroscopy

Ans.

Spectroscopy, organic naming reactions, and various spectroscopic techniques are important in chemistry.

  • Spectroscopy is the study of the interaction between matter and electromagnetic radiation.

  • Organic naming reactions involve the naming of organic compounds based on their functional groups and substituents.

  • HPLC (High Performance Liquid Chromatography) is a technique used to separate and analyze components in a mixture.

  • IR (Infrared) spectroscopy is used to identify functional...read more

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Q2. What is Data integrity?

Ans.

Data integrity refers to the accuracy, consistency, and reliability of data throughout its lifecycle.

  • Data must be complete, accurate, and consistent

  • Data must be protected from unauthorized access or modification

  • Data must be available when needed

  • Examples include financial records, medical records, and scientific research data

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Q3. Tell us about GLP

Ans.

GLP stands for Good Laboratory Practice and is a set of guidelines for ensuring quality and reliability in non-clinical laboratory studies.

  • GLP is a regulatory requirement for non-clinical studies conducted for the development of pharmaceuticals, chemicals, and other products.

  • It covers all aspects of the study, including the study design, conduct, data collection, analysis, and reporting.

  • GLP ensures that the study is conducted in a consistent and reliable manner, and that the ...read more

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Q4. What is alcoa plus

Ans.

Alcoa Plus is a brand of aluminum composite material used in construction.

  • Alcoa Plus is a type of aluminum composite material (ACM) used in building facades and cladding.

  • It is known for its durability, lightweight, and fire-resistant properties.

  • Alcoa Plus panels consist of two aluminum sheets bonded to a non-aluminum core, such as polyethylene.

  • The panels come in a variety of colors and finishes, including metallic and wood grain.

  • Alcoa Plus has been used in many high-profile b...read more

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Q5. Tell us about GMP

Ans.

GMP stands for Good Manufacturing Practice, a set of guidelines ensuring the quality and safety of pharmaceutical products.

  • GMP is a regulatory framework that governs the production, testing, and distribution of pharmaceutical products.

  • It ensures that pharmaceutical companies follow standardized procedures to maintain product quality and safety.

  • GMP covers various aspects such as facility design, equipment validation, personnel training, documentation, and quality control.

  • Adher...read more

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Q6. Calibration of Gc and HPLC

Ans.

Calibration of GC and HPLC is essential for accurate and reliable results.

  • Calibration involves adjusting the instrument to ensure accurate measurements.

  • It is important to use certified reference materials for calibration.

  • Calibration should be performed regularly to maintain instrument accuracy.

  • Documentation of calibration procedures and results is necessary for quality control.

  • Examples of calibration parameters include retention time, peak area, and resolution.

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Q7. What is the validation

Ans.

Validation is the process of ensuring that data or results are accurate and reliable.

  • Validation involves checking and verifying data or results through various methods.

  • It helps to ensure that the data or results are free from errors, inconsistencies, and biases.

  • Validation can be done through manual checks, automated tests, or statistical analysis.

  • Examples of validation include checking the accuracy of survey responses, verifying the results of a scientific experiment, or test...read more

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Q8. Different types of QMS documents

Ans.

Different types of QMS documents include policies, procedures, work instructions, forms, records, and manuals.

  • Policies: high-level statements of intent and direction

  • Procedures: step-by-step instructions for carrying out processes

  • Work instructions: detailed instructions for specific tasks

  • Forms: templates for documenting information

  • Records: documented evidence of activities or results

  • Manuals: comprehensive guides to the QMS

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Q9. Plant Process and Experience

Ans.

I have over 10 years of experience in plant process optimization, including implementing new technologies and improving efficiency.

  • Implemented new technologies to improve plant efficiency

  • Optimized plant processes to reduce waste and increase productivity

  • Led teams in troubleshooting and resolving plant process issues

  • Developed and implemented training programs for plant staff

  • Collaborated with cross-functional teams to drive continuous improvement initiatives

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Q10. Type of validation

Ans.

Validation is the process of ensuring that data is accurate and reliable.

  • Validation can be done through data entry controls, such as range checks and format checks.

  • Validation can also involve cross-referencing data with external sources or previous records.

  • Examples of validation include verifying email addresses, checking for duplicate entries, and confirming payment details.

  • Validation helps to prevent errors and ensure the integrity of data.

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