Annora Pharma Senior Executive QA Interview Questions and Answers

HPLC and GC are analytical techniques used to separate, identify, and quantify components in a mixture.

• HPLC (High Performance Liquid Chromatography) is used for separating compounds in a liquid mixture based on their interaction with a stationary phase and a mobile phase.

• GC (Gas Chromatography) is used for separating compounds in a gas mixture based on their partitioning between a stationary phase and a mobile phase.

• Bo...read more

HPLC is used to determine the presence and quantity of various substances in a sample.

• HPLC stands for High Performance Liquid Chromatography.

• It is commonly used in pharmaceutical, environmental, and food industries.

• HPLC separates and analyzes compounds in a sample based on their interactions with a stationary phase and a mobile phase.

• It is a powerful tool for identifying and quantifying components in complex mixtures.

• E...read more

Quality plays a critical role in ensuring the sterility and safety of products in aseptic areas.

• Ensuring compliance with regulatory requirements for aseptic processing

• Implementing and monitoring aseptic techniques and procedures

• Performing regular environmental monitoring to detect any contamination

• Training personnel on proper aseptic practices

• Investigating and addressing any deviations or failures in aseptic processes

My expectation for salary is competitive based on my experience and skills. I am looking for a challenging job role where I can utilize my QA expertise.

• Expectation for competitive salary based on experience and skills

• Looking for a challenging job role to utilize QA expertise

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...read more

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...read more

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...read more

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...read more

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...read more

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...read more

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...read more

Reviews of PVR and PQRS can be conducted through a systematic process involving data analysis and evaluation.

• Collect and analyze data related to PVR and PQRS

• Evaluate the performance and quality based on established criteria

• Identify areas of improvement and develop action plans

• Implement changes and monitor the impact

• Continuously review and update the process to ensure ongoing quality assurance

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