Nokia Interview Questions and Answers

The limits of weight variations in QA officer role.

• Weight variations should be within a specified range to ensure product quality.

• Limits are determined based on industry standards and product specifications.

• Regular weight checks are conducted to monitor variations and ensure compliance.

• Examples of weight variations limits include +/- 5 grams for packaged food products.

• QA officers play a crucial role in maintaining weight standards and identifying deviations.

A tablet is a solid dosage form of medication that is compressed into a small, flat shape for easy swallowing.

• Tablets are one of the most common forms of medication.

• They are made by compressing a mixture of active ingredients and excipients.

• Tablets can be coated to make them easier to swallow or to protect the active ingredients from degradation.

• Different types of tablets include immediate-release, extended-release, and chewable tablets.

• Examples of tablets include aspirin, ib...read more

The number of personnel required for QMS activities depends on the size and complexity of the organization.

• The number of personnel needed for QMS activities can vary based on the size of the organization.

• Complexity of QMS activities also plays a role in determining the required team size.

• A small organization may only need a few individuals to manage QMS activities, while a large organization may require a dedicated team.

• Roles within the team may include Quality Manager, Quali...read more

Tablets are solid dosage forms that contain medicinal substances and are intended for oral administration.

• Immediate-release tablets

• Extended-release tablets

• Chewable tablets

• Effervescent tablets

• Sublingual tablets

• Buccal tablets

• Enteric-coated tablets

• Film-coated tablets

• Dispersible tablets

Take immediate action to investigate the cause and rectify the parameter back within limits.

• Identify the root cause of the parameter going out of limit

• Implement corrective actions to bring the parameter back within limits

• Monitor the parameter closely to ensure it stays within limits

• Document the incident and actions taken for future reference

I am very willing to prepare documentation for manufacturing processes.

• I have experience creating and organizing manufacturing documents such as work instructions, SOPs, and batch records.

• I am detail-oriented and ensure all necessary information is included in the documentation.

• I am proficient in using software tools like Microsoft Office and ERP systems to create and manage manufacturing documents.

• I understand the importance of accurate and up-to-date documentation in ensuri...read more

Validation is the process of ensuring that a system or product meets the specified requirements and standards.

• Types of validation include: functional validation, performance validation, security validation, usability validation, and compliance validation.

• Functional validation ensures that the system or product meets the functional requirements.

• Performance validation ensures that the system or product meets the performance requirements.

• Security validation ensures that the syst...read more

I have experience in developing products for regulated markets and international exposure with different dosage forms.

• Developed products for FDA regulated markets and obtained approvals

• Launched products in international markets including Europe and Asia

• Experience in developing various dosage forms such as tablets, capsules, and injectables

• Ensured compliance with regulatory requirements and guidelines

• Collaborated with cross-functional teams to ensure successful product develop...read more