pharma qc interview questions and answers pdf

Pharma Qc Interview Questions And Answers Pdf

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At the same time those who are able to overcome the fear of exposure, are certain to be successful in any case.

Filming is a slow form of sticking and is largely due to excess moisture in the granulation. Q What is the standard number of rotations used for friability test? Q What is the fall height of the tablets in the friabilator during friability testing?

Quality Control. Quality Control is used for testing the software products. Making big decisions is a large part of being a QC Inspector. Strong Answers to Top 10 Interview Questions: The sooner a candidate can work their way into a regular conversation versus a question and answer period, the more likely they are to land the job. Using a soft lead pencil 2 or softer only, blacken the circle of the correct answer.

41 Pharmaceutical Quality Control Interview Questions & Answers

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SlideShare Explore Search You. Submit Search. Home Explore. Successfully reported this slideshow. We use your LinkedIn profile and activity data to personalize ads and to show you more relevant ads. You can change your ad preferences anytime. Upcoming SlideShare.

Like this presentation? Why not share! Embed Size px. Start on. Show related SlideShares at end. WordPress Shortcode. Pristyn Research Solutions Follow. Full Name Comment goes here. Are you sure you want to Yes No. Rishi Sai Kiran. Purna Yalla. Show More. No Downloads. Views Total views. Actions Shares. No notes for slide. Q 1- What are the contents of the SOP? Q 2-What is the difference between intermediate and drug substance API?

Ans- Intermediate: A material produced during steps of the processing of an API that undergoes further molecular change or purifications before it become an API API: Any substance or mixture of substances intended to be used in the manufacturing of a drug medicinal product and that when used in the production of a drug, becomes an API of the drug product.

Q 3-What is documentation? Ans-All the written production procedures, instructions and records, quality control procedures and recorded test results involved in the manufacturing of a medicinal product.

Ans-The sum total of the organized arrangements made with the objects of ensuring that all APIs are of the quality required for their intended use and the quality systems are maintained. Q 5-What is cGMP? Ans-Current Good Manufacturing Practices. Q 6-How are cGMP implemented?

Q 7-What is the different types of Qualifications and write its flow? Q 9-How many types of raw material and packing material? Ans- Raw materials are classified into two types. Those are as follows: 1. Other raw material Packing materials are classified into two types. Primary Packing material 2. Ans-Out of Specification OOS results are those results, generated during testing that do not comply with the relevant specification or standards or with the defined acceptance criteria.

Q What is limit of Temperature and relative humidity in the pharma area? Ans-The demonstration that a particular instrument or device produces results within specified limits by comparison with results produced by a reference or traceable standard over an appropriate range of measurements. Q Why cGMP should be followed? Ans-This is a regulation that each one of us is trained in cGMP and practices cGMP - It minimizes the possibilities of any errors caused by subjectivity.

Q Why do we conduct trainings? Ans-It brings awareness and helps us in becoming competent. Q What do you mean by Critical Quality Attributes? Ans-A critical quality attributes is a physical, chemical, biological or microbiological property or characteristic that should be within an appropriate limit, range, or distribution to ensure the desired product quality.

Q What do you mean by production? What Is The Hplc Principle? Ans- It is a technique used for separating the mixture of components into individual components based on adsorption, partition, ion exchange and size exclusion principles. Stationary phase and mobile phase used in it. HPLC used for identification, quantification and purification of components form a mixture.

Explain Hplc Instrumentation? Firstly, solvent mobile phase is degassed for eliminating the bubbles. It is passed through the pump with a uniform pressure. The liquid sample is injected into the mobile phase flow stream. It passes through the stationary phase identified by the detectors and recorded. Question What Is Room Temperature? Ans- 25 degree centigrade Q Ans- UV spectroscopy range nm, Visible spectroscopy range nm to nm. Ans- Spectroscopy used for detecting the functional groups, impurities.

Qualitative and quantitative analysis can be done. Ans- Qualitative analysis involves identification of the compound or chemical based on their chemical absorption, emission or physical properties e. Quantitative analysis involves estimation or determination of concentration or amount of the chemical compounds or components. Ans- UV spectroscopy uses light in the UV part of electromagnetic spectrum.

UV absorption spectra arises in which molecule or atoms outer electrons absorb energy, undergoes transition from lower energy level to higher energy level. For each molecule, absorbance at wavelength is specific Q Explain About Beer Lamberts Law?

Ans- It states that the intensity of monochromatic light absorbed by a substance dissolved in a fully transmitting solvent is directly proportional to the substance concentration and the path length of the light through the solution.

Explain the difference between QC and QA? Ans QA provides the confidence that a product will full fill the quality requirements.

QC determines and measures the product quality level. What are types of climatic zones? India belongs to which climatic zone? It is a USFDA regulations to assure proper design , manufacturing and control of manufacturing processes and services. These are the standard guidelines given by Food and Drug administration to make sure that a product is manufactured with safety and quality. It refers to recent and advance updates to these standard guidelines. Step by step manufacturing process and details about batch recorded here.

BPR is depends on packaging operation. What do you know about stability studies? Ans These are necessary for developing the pharmaceutical products. It helps to evaluate the effect of environmental factors e. Expand ICH? Tell me about ICH Guidelines?

It brings the regulatory authorities and pharmaceutical companies together to discuss the drug registration technical aspects. The aim of the ICH is to enhance the harmonization world wide to make sure that safe, high quality and effective drugs are developed and registered in the most efficient manner.

ICH provides guidelines on 4 aspects that is quality , safety , Efficacy and Multidisciplinary guidelines. What is the time period required for long term and accelerated stability studies? Ans Long term 12 months, Accelerated studies- 6 months You just clipped your first slide!

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Quality Control Executive Interview Questions & Answers

Below are some Interview Questions and answers which can help the freshers as well as experience personnel for interview preparation so please Read and share if you think it useful. Disintegration is to be Performed to determine whether tablets or capsules disintegrate within the prescribed time when placed in a liquid medium at the experimental conditions. Friability is defined as the percentage of weight loss of powder from the surface of the tablets due to mechanical action and the test is performed to measure the weight loss during transportation. Tablets with individual weight equal to or less than mg then take the sample of whole corresponding to as near as 6. Tablets must be de-dusted prior to and after use. Any unplanned or uncontrolled event in the form of non-compliance to the designed systems or procedures at any stage of testing, and storage of drug product due to system failure or equipment breakdown or manual error.

Slideshare uses cookies to improve functionality and performance, and to provide you with relevant advertising. If you continue browsing the site, you agree to the use of cookies on this website. See our User Agreement and Privacy Policy. See our Privacy Policy and User Agreement for details. Published on Jan 30, Email: info pristynresearch.

Pharma Quality Control Interview Question and Answers

Quality control executive interview questions and answersYou can use free Quality control executive interview questions below to ask candidates or self-answer in a job interview for Quality control executive. Please note that you also use interview questions and answers, interview tips, types of job interview, interview thank letters …at sidebar. You can use free Quality control executive interview questions below to ask candidates or self-answer in a job interview for Quality control executive.

QC pharma jobs offered for b pharmacy freshers in pharmaceutical industry. Usually, first you should qualify an interview exam for attending the interview. It is depend upon the which pharmaceutical company you are trying for.

quality control exam questions and answers pdf

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Pharma Quality Control Interview Questions & Answers

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Michael M.

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