Teva Pharmaceuticals
Proud winner of ABECA 2024 - AmbitionBox Employee Choice Awards
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I applied via Recruitment Consulltant and was interviewed before Dec 2023. There were 3 interview rounds.
I have extensive technical knowledge in Quality Management Systems (QMS) and Good Manufacturing Practices (GMP).
Certified in ISO 9001 and other relevant quality management standards
Experience in implementing and maintaining QMS in previous roles
Knowledge of FDA regulations and GMP guidelines
Skilled in conducting internal audits and ensuring compliance with quality standards
Continuous improvement mindset to enhance qual
I have extensive technical knowledge of the guidelines and processes performed on the shop floor.
Proficient in understanding and implementing quality control measures
Familiar with lean manufacturing principles and continuous improvement techniques
Skilled in using various tools and equipment on the shop floor
Knowledgeable about safety protocols and regulations in a manufacturing environment
I applied via Walk-in and was interviewed before Jan 2019. There were 3 interview rounds.
I applied via Referral and was interviewed before Aug 2021. There was 1 interview round.
AAS principle refers to the three key elements of authentication, authorization, and accounting in information security.
Authentication: verifying the identity of a user or system
Authorization: granting access to specific resources based on the user's identity and permissions
Accounting: tracking and logging user activity for auditing and compliance purposes
Example: A user logging into a system with a username and passwo...
I applied via Campus Placement and was interviewed before Feb 2020. There were 3 interview rounds.
My biggest achievement till date is successfully leading a team to launch a new product that generated $10 million in revenue within the first year.
Successfully led a team to launch a new product
Generated $10 million in revenue within the first year
Implemented effective marketing strategies to drive product adoption
Managed cross-functional teams and ensured smooth execution
Received recognition and appreciation from sen
I applied via Naukri.com and was interviewed before Nov 2022. There were 2 interview rounds.
Forced degradation study is a process used to determine the stability of a drug substance or product under various stress conditions.
Forced degradation studies involve subjecting the drug to conditions such as heat, light, humidity, and acid/base hydrolysis to simulate potential degradation pathways.
The purpose of these studies is to identify degradation products, determine degradation pathways, and establish the stabi...
Validation parameters are criteria used to ensure data input meets specified requirements.
Validation parameters can include data type, length, format, range, and presence.
For example, a validation parameter for a phone number field may require 10 digits and no special characters.
Validation parameters help prevent errors and ensure data integrity.
They are commonly used in form fields and database entries.
Validations in executive roles can face challenges due to lack of data accuracy, timeliness, and stakeholder alignment.
Data accuracy issues can lead to incorrect decisions being made.
Timeliness of data can impact the speed at which decisions can be made.
Lack of stakeholder alignment can result in conflicting priorities and goals.
Inconsistent validation processes across departments can lead to discrepancies in data inte
A validation plan outlines the process for ensuring that a product or system meets specified requirements and standards.
Defines the objectives and scope of validation activities
Identifies the resources, responsibilities, and timelines for validation
Specifies the methods and procedures for testing and evaluating the product or system
Includes criteria for acceptance and rejection of validation results
Calibration of HPLC is a process of adjusting the settings of the High Performance Liquid Chromatography system to ensure accurate and reliable results.
Calibration involves checking and adjusting the flow rate, detector sensitivity, and column efficiency.
Regular calibration helps maintain the accuracy and precision of the HPLC system.
Calibration standards are used to verify the performance of the system.
Documentation o...
I applied via Referral and was interviewed before Jan 2023. There was 1 interview round.
I applied via Approached by Company and was interviewed before Apr 2023. There was 1 interview round.
Data integrity refers to the accuracy, consistency, and reliability of data throughout its lifecycle.
Ensures data is accurate and reliable
Prevents unauthorized access or changes
Maintained through data validation and verification processes
I appeared for an interview before Dec 2023.
APQR conclusion is the final assessment and summary of the Annual Product Quality Review.
APQR conclusion is a comprehensive evaluation of the quality of a product over the course of a year.
It includes analysis of data, trends, deviations, and any corrective actions taken.
The conclusion may recommend changes to processes, formulations, or quality control measures.
Examples of APQR conclusions could be recommendations for...
OOS flow refers to the out of stock flow in retail operations.
OOS flow occurs when a product is not available for purchase due to being out of stock.
It is important for retailers to manage OOS flow effectively to avoid losing sales and customer dissatisfaction.
Strategies to address OOS flow include improving inventory management, implementing automated restocking systems, and setting up alerts for low stock levels.
Line clearance is the process of ensuring that a production line is free from any previous product or material before starting a new production run.
Ensure all equipment is clean and sanitized before starting a new production run
Verify that all materials and ingredients are correct and properly labeled
Check that all previous product residue is removed from the production line
Confirm that all necessary quality checks hav
Stability conditions refer to the factors that contribute to the overall stability of a system or organization.
Stability conditions can include financial stability, political stability, and social stability.
In a business context, stability conditions may involve having a strong leadership team, a solid customer base, and a diversified product line.
For a government, stability conditions could include a stable economy, e...
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Interview experience
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Rating in categories
Executive
101
salaries
| ₹3 L/yr - ₹11 L/yr |
Senior Executive
89
salaries
| ₹4 L/yr - ₹12 L/yr |
Regulatory Affairs Associate
79
salaries
| ₹4 L/yr - ₹11 L/yr |
Senior Quality Specialist
78
salaries
| ₹3 L/yr - ₹9.2 L/yr |
Assistant Manager
67
salaries
| ₹8.4 L/yr - ₹20.3 L/yr |
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