Bliss Gvs Pharma
10+ Concentrix Corporation Interview Questions and Answers
Q1. What is the process for the calibration of High-Performance Liquid Chromatography (HPLC)?
Calibration of HPLC involves preparing standard solutions, running them through the system, adjusting parameters, and verifying results.
Prepare standard solutions of known concentrations.
Run the standard solutions through the HPLC system.
Adjust parameters such as flow rate, column temperature, and detector wavelength.
Verify the results by comparing the peak areas or retention times with known standards.
Document the calibration process and results for traceability.
Q2. What is the difference between an assay and content uniformity?
Assay measures the potency or concentration of a drug, while content uniformity ensures consistent distribution of active ingredients in a dosage form.
Assay determines the amount of a specific substance in a sample, such as the active ingredient in a drug.
Content uniformity checks the distribution of active ingredients throughout a dosage form to ensure consistency.
Assay is usually expressed as a percentage or concentration, while content uniformity is assessed based on the u...read more
Q3. What are the various types of dissolution?
Various types of dissolution include intrinsic dissolution, dissolution rate, and dissolution efficiency.
Intrinsic dissolution: measures the dissolution rate of a pure substance under standardized conditions.
Dissolution rate: measures the amount of substance that dissolves over time.
Dissolution efficiency: measures the extent to which a substance dissolves in a given solvent.
Other types include surface dissolution, bulk dissolution, and controlled release dissolution.
Examples...read more
Q4. What is HPLC and its principle?
HPLC stands for High Performance Liquid Chromatography. It is a technique used to separate, identify, and quantify components in a mixture.
HPLC involves a sample being dissolved in a solvent and then pumped through a column packed with a stationary phase.
Different components in the sample interact differently with the stationary phase, leading to separation based on their properties.
The separated components are detected and quantified as they exit the column.
HPLC is commonly ...read more
Q5. What is difference between hardness and compaction force
Hardness refers to the resistance of a material to deformation, while compaction force is the force applied to compact a material.
Hardness is a measure of how resistant a material is to scratching or indentation.
Compaction force is the force applied to compress or compact a material, such as in soil compaction.
Hardness is typically measured using tests like Rockwell or Vickers hardness tests.
Compaction force is often measured in pounds or newtons depending on the application....read more
Q6. What is the procedure for sampling of blend sample
Sampling of blend sample involves following a specific procedure to ensure accuracy and representativeness.
Ensure the blend is homogenized before sampling
Use a sampling thief or probe to collect samples from multiple locations
Follow a predetermined sampling plan to ensure randomness
Record all sampling details including location, time, and quantity
Transfer samples to appropriate containers for testing
Q7. What is procedure of in process test of tablet
In process testing of tablets involves conducting tests at various stages of production to ensure quality and consistency.
In process testing includes checks on raw materials, formulation, and physical characteristics of tablets.
Tests may include weight variation, hardness, disintegration, and dissolution tests.
Results are compared to predefined specifications to determine if the tablets meet quality standards.
Any deviations from specifications are investigated and corrective ...read more
Q8. What is the procedure for sampling
Sampling procedure involves selecting a representative portion of a larger group for testing or analysis.
Identify the population or group to be sampled
Determine the sampling method (random, stratified, etc.)
Select the sample size based on statistical considerations
Collect the samples using appropriate techniques
Ensure proper labeling and documentation of samples
Transport samples to the testing facility in a timely manner
Q9. What is 21 CFR?
21 CFR is a set of regulations established by the Food and Drug Administration (FDA) in the United States to ensure the quality and safety of food, drugs, and medical devices.
21 CFR stands for Title 21 of the Code of Federal Regulations.
It covers regulations related to food and drugs, including Good Manufacturing Practices (GMP), labeling requirements, and quality control standards.
Compliance with 21 CFR is mandatory for companies involved in the production, distribution, and...read more
Q10. How can you increase revenue to our organization.
Increasing revenue can be achieved by optimizing patient care, improving efficiency, and expanding services.
Implementing cost-effective strategies to reduce expenses
Increasing patient volume through marketing and outreach efforts
Expanding services offered to attract more patients
Improving patient satisfaction to encourage repeat business
Streamlining administrative processes to increase efficiency
Q11. experience in imparting training's
I have over 10 years of experience in designing and delivering training programs for various levels of employees.
Designed and implemented training programs tailored to specific job roles and skill levels
Utilized a variety of training methods such as workshops, online modules, and on-the-job training
Evaluated training effectiveness through feedback surveys and performance metrics
Collaborated with subject matter experts to ensure training content was accurate and up-to-date
Q12. Earlier Company's experience
Interview Process at Concentrix Corporation
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