Apitoria Pharma
10+ Startek Interview Questions and Answers
Q1. What is the principal UVvisible spector photo meter
The principal UV-visible spectrophotometer is a scientific instrument used to measure the absorption of light by a sample in the ultraviolet and visible regions of the electromagnetic spectrum.
UV-visible spectrophotometers are commonly used in analytical chemistry, biochemistry, and pharmaceutical industries.
They are used to determine the concentration of a sample by measuring how much light it absorbs at different wavelengths.
Examples of popular UV-visible spectrophotometers...read more
Q2. Explain Data back up and Analytical data review procedure
Data backup involves regularly saving copies of data to prevent loss, while analytical data review is the process of examining and interpreting data for insights.
Data backup involves creating duplicate copies of data to ensure it is not lost in case of system failure or other issues.
Analytical data review includes examining data sets to identify trends, patterns, and insights that can inform decision-making.
Regularly scheduled backups should be performed to ensure data is up-...read more
Q3. What is the principal of polari meter
A polarimeter is a scientific instrument used to measure the angle of rotation of polarized light as it passes through a substance.
Polarimeters are commonly used in chemistry to determine the concentration and purity of optically active substances.
The principle of a polarimeter is based on the ability of chiral molecules to rotate the plane of polarized light.
The angle of rotation is measured using a polarizer, a polarized light source, and a detector.
The specific rotation of...read more
Q4. What is cGmp and MR meter calibration
cGMP stands for current Good Manufacturing Practice, which are regulations enforced by the FDA to ensure quality in pharmaceutical production. MR meter calibration is the process of ensuring accuracy in measuring devices.
cGMP is a set of regulations enforced by the FDA to ensure quality in pharmaceutical manufacturing
MR meter calibration is the process of adjusting and verifying the accuracy of measuring devices like MR meters
Both cGMP and MR meter calibration are important i...read more
Q5. How performed KF R factor
KF R factor analysis is performed by calculating the ratio of the observed variance to the expected variance in a factor analysis model.
Calculate the ratio of the observed variance to the expected variance for each factor in the factor analysis model.
The KF R factor analysis helps in determining the goodness of fit of the factor model.
Higher KF R values indicate a better fit between the observed data and the factor model.
Q6. How to requite the manpower.
Manpower can be requited by offering competitive salaries, providing opportunities for growth and development, creating a positive work environment, and recognizing and rewarding employees' contributions.
Offer competitive salaries to attract and retain top talent
Provide opportunities for growth and development through training programs and career advancement
Create a positive work environment with open communication, teamwork, and a healthy work-life balance
Recognize and rewar...read more
Q7. Explain OOS investigation flow
OOS investigation flow involves identifying, investigating, and resolving deviations from specifications.
Identify the OOS result through testing or monitoring
Investigate the root cause of the deviation
Implement corrective actions to prevent recurrence
Document the investigation process and findings
Review and approve the investigation report
Q8. How much vacuum build in Hyderabad
The vacuum build in Hyderabad varies depending on the location and time of measurement.
Vacuum levels in Hyderabad can range from 700 to 760 mmHg
Factors such as altitude, weather conditions, and equipment used can affect vacuum levels
For example, in a laboratory setting, a vacuum pump may be used to create a vacuum for experiments
Q9. How to open vacuum tray dryer.
To open a vacuum tray dryer, follow these steps carefully.
Ensure the vacuum tray dryer is turned off and disconnected from power source.
Release any pressure inside the dryer by slowly opening the vent valve.
Unlock and open the door of the vacuum tray dryer.
Carefully remove the trays one by one, starting from the top.
Inspect the trays for any residue or product buildup and clean if necessary.
Close the door securely after removing or loading trays.
Reconnect the power source and...read more
Q10. What are the measures involved in the process development of an Active Pharmaceutical Ingredient (API)?
Measures involved in process development of an API include optimization of synthetic route, selection of raw materials, purification techniques, and analytical method development.
Optimization of synthetic route to improve yield and reduce impurities
Selection of high-quality raw materials to ensure consistency and purity of the final product
Development of purification techniques such as crystallization, distillation, or chromatography
Analytical method development for testing t...read more
Q11. How to operate reactors
Reactors are operated by following standard operating procedures, monitoring key parameters, adjusting conditions as needed, and ensuring safety protocols are followed.
Follow standard operating procedures provided by the manufacturer or company
Monitor key parameters such as temperature, pressure, flow rate, and pH regularly
Adjust conditions as needed to maintain desired reaction conditions
Ensure safety protocols are followed at all times to prevent accidents
Keep detailed reco...read more
Q12. What is exothermic reaction
An exothermic reaction is a chemical reaction that releases energy in the form of heat.
Exothermic reactions release heat to the surroundings
They have a negative change in enthalpy (ΔH)
Examples include combustion reactions, neutralization reactions, and some oxidation reactions
Q13. What is clean room
A clean room is a controlled environment with low levels of pollutants such as dust, airborne microbes, aerosol particles, and chemical vapors.
Clean rooms are typically used in industries such as pharmaceuticals, biotechnology, electronics, and aerospace.
They are designed to maintain a specific level of cleanliness to ensure the quality of products being manufactured.
Clean rooms have strict protocols for entry, including wearing special clothing like gowns, gloves, masks, and...read more
Q14. What we do the daily work plan and analysis procedure
Daily work plan involves setting goals, prioritizing tasks, analyzing data, and implementing improvements.
Create a daily work plan outlining tasks and goals
Prioritize tasks based on importance and deadlines
Analyze data collected from quality control processes
Identify areas for improvement and implement changes
Review and adjust work plan as needed
Q15. How to improve quality
Improving quality involves setting clear standards, continuous monitoring, feedback loops, and employee training.
Establish clear quality standards and guidelines
Implement regular quality checks and audits
Encourage feedback from customers and employees
Provide training and development opportunities for employees to enhance skills and knowledge
Q16. Chemistry of uv spectroscopy
UV spectroscopy is a technique that uses ultraviolet light to measure the absorption, transmission, and emission of molecules.
UV spectroscopy involves the use of ultraviolet light in the range of 190-400 nm.
It is commonly used to analyze the electronic transitions in organic molecules.
UV spectroscopy can provide information about the structure, purity, and concentration of a sample.
The Beer-Lambert Law is often used in UV spectroscopy to relate absorbance to concentration.
UV ...read more
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