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I applied via Walk-in and was interviewed before Aug 2021. There were 3 interview rounds.
Line clearance is a process of ensuring that equipment and work areas are free from any previous product or material before starting a new process.
It involves a visual inspection of the equipment and work area to ensure cleanliness and absence of any residual material.
It is important to prevent cross-contamination and ensure product quality.
Examples include cleaning of manufacturing equipment, changeover of packaging m...
In process control is a system of checks and measures to ensure quality and consistency during the manufacturing process.
In process control involves monitoring and adjusting variables such as temperature, pressure, and pH levels to maintain quality standards.
It includes sampling and testing of raw materials, intermediates, and finished products to ensure they meet specifications.
Examples of in process control technique...
I appeared for an interview in Nov 2024.
I appeared for an interview in Feb 2025, where I was asked the following questions.
Quality control ensures products meet specified standards through systematic testing and evaluation.
Involves processes to maintain desired levels of quality in products.
Includes inspections, testing, and audits to identify defects.
Example: In manufacturing, products are tested for durability and safety.
Utilizes statistical methods to monitor and improve processes.
Example: Control charts track variations in production t
Quality control ensures products meet standards, enhancing reliability, safety, and customer satisfaction.
Improves product consistency: Ensures that products are uniform in quality, e.g., a beverage company maintaining taste across batches.
Reduces defects: Identifies and eliminates defects in manufacturing, such as a car manufacturer catching flaws in assembly.
Enhances customer satisfaction: By delivering high-quality ...
Quality control encompasses various methods to ensure products meet specified standards and requirements.
1. Statistical Quality Control (SQC) - Uses statistical methods to monitor and control processes. Example: Control charts.
2. Quality Assurance (QA) - Focuses on preventing defects through planned and systematic activities. Example: ISO 9001 standards.
3. Total Quality Management (TQM) - An organization-wide approach ...
I applied via Naukri.com and was interviewed in Sep 2024. There was 1 interview round.
Regulatory bodies are organizations that enforce laws and regulations to ensure compliance and safety in various industries.
Regulatory bodies set standards and guidelines for companies to follow
They monitor and inspect businesses to ensure compliance with regulations
Examples include FDA in the pharmaceutical industry and EPA in the environmental sector
Gland Pharma interview questions for popular designations
I appeared for an interview in Feb 2025, where I was asked the following questions.
Molarity is a measure of concentration, defined as moles of solute per liter of solution.
Molarity (M) = moles of solute / liters of solution.
Example: 1 M NaCl solution contains 1 mole of NaCl in 1 liter of water.
Used in chemistry to prepare solutions with precise concentrations.
Important for stoichiometric calculations in reactions.
Detectors in HPLC identify and quantify compounds as they elute from the column, crucial for analysis.
UV-Visible Detector: Measures absorbance of UV/visible light; commonly used for organic compounds.
Fluorescence Detector: Detects compounds that fluoresce; highly sensitive for trace analysis.
Refractive Index Detector: Measures changes in refractive index; useful for non-UV absorbing compounds.
Conductivity Detector: Mea...
Normality is a measure of concentration equivalent to the number of equivalents of solute per liter of solution.
Normality (N) is defined as the number of equivalents of solute per liter of solution.
It is commonly used in acid-base reactions, where 1 N solution of HCl can donate 1 equivalent of H+ ions.
For example, a 1 N solution of sulfuric acid (H2SO4) provides 2 equivalents of H+ ions per mole.
Normality is particular...
The molecular weight of oxygen (O2) is approximately 32 g/mol, calculated from its atomic mass.
Oxygen exists primarily as O2, a diatomic molecule.
The atomic mass of a single oxygen atom is about 16 g/mol.
Thus, for O2: 16 g/mol (O) x 2 = 32 g/mol.
Molecular weight is crucial in stoichiometry for chemical reactions.
The Diels-Alder reaction is a cycloaddition between a diene and a dienophile to form a six-membered ring.
Involves a diene (e.g., 1,3-butadiene) and a dienophile (e.g., maleic anhydride).
Forms a cyclohexene derivative as the product.
It is a [4+2] cycloaddition reaction.
Used in the synthesis of complex organic molecules.
Example: The reaction of 1,3-butadiene with maleic anhydride yields cyclohexene derivatives.
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I applied via Campus Placement and was interviewed in Mar 2024. There was 1 interview round.
TLC stands for Thin Layer Chromatography, a technique used to separate and analyze mixtures of chemicals.
TLC involves a stationary phase (thin layer of adsorbent material) and a mobile phase (solvent).
The sample mixture is spotted on the TLC plate and the plate is placed in a developing chamber with the mobile phase.
Different components of the mixture move at different rates on the plate, allowing for separation and id...
Disintegration is the breakdown of a solid dosage form into smaller particles, while dissolution is the process by which a solid substance dissolves in a liquid.
Disintegration is a physical process, while dissolution is a chemical process.
Disintegration involves the breaking down of a tablet or capsule into smaller pieces, while dissolution involves the solubilization of the active ingredient.
Disintegration testing is ...
Vial washing and depyrogenation tunnel
I applied via Walk-in and was interviewed in May 2024. There were 2 interview rounds.
I applied via Approached by Company and was interviewed in Aug 2023. There were 3 interview rounds.
Change control is a process used to manage and document changes to a system or process.
Change control ensures that changes are properly reviewed, approved, and implemented.
It helps to minimize risks and ensure that changes do not negatively impact the quality or functionality of the system.
Change control typically involves documenting the change request, assessing its impact, obtaining necessary approvals, implementing...
Process validation is the process of establishing documented evidence that a process consistently produces a product meeting predetermined specifications.
There are three types of process validation: prospective validation, concurrent validation, and retrospective validation.
Prospective validation is conducted before the process is put into routine use.
Concurrent validation is performed during routine production.
Retrosp...
Audit trail is maintained by documenting and tracking all activities and changes made to a system or process.
Audit trail is created by recording all actions, events, and transactions that occur within a system.
It helps in ensuring accountability, traceability, and compliance with regulations.
Audit trail can be established through the use of logs, timestamps, and version control.
It is important to capture relevant infor...
Yes, I am interested in Microbiology analytical review.
I have a strong background in microbiology and enjoy analyzing data in this field.
I have experience conducting microbiological tests and interpreting the results.
I am familiar with various microbiological techniques and methodologies.
I am interested in staying updated with the latest advancements in microbiology research.
I believe that my knowledge and skills in mi...
Purified water specification refers to the set of requirements and standards that purified water must meet.
Purified water should have a low level of impurities, such as minerals, chemicals, and microorganisms.
It should meet the specifications outlined by regulatory bodies, such as the United States Pharmacopeia (USP) or European Pharmacopoeia (EP).
The pH level of purified water should be within a specific range, typica...
The purified water specification for microbial quality assurance.
Microbial specification for purified water is crucial to ensure its safety and suitability for use.
The specification typically includes limits for various microorganisms, such as bacteria, fungi, and endotoxins.
Commonly used tests for microbial quality assessment include total viable count, microbial identification, and endotoxin testing.
The specification...
Validation is the process of evaluating a system or component during or at the end of the development process to determine whether it satisfies specified requirements.
Functional Validation: Ensuring that the system meets the functional requirements.
Performance Validation: Verifying that the system performs as expected under different load conditions.
Security Validation: Checking the system for vulnerabilities and ensur...
I applied via Naukri.com and was interviewed in Jun 2023. There were 2 interview rounds.
The duration of Gland Pharma interview process can vary, but typically it takes about less than 2 weeks to complete.
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