R L Fine Chem Senior Manager Interview Questions and Answers

To prepare the QC laboratory for an audit, follow these steps:

• Ensure all equipment is calibrated and validated

• Review and update standard operating procedures (SOPs)

• Train laboratory personnel on audit procedures and expectations

• Perform internal audits to identify and address any non-compliance issues

• Organize and maintain documentation, including records of test results and equipment maintenance

• Implement a robust quality...read more

An OOS investigation is a process to determine the cause of an out-of-specification result in a product or process.

• OOS stands for Out-of-Specification.

• It involves a thorough investigation to identify the root cause of the deviation.

• The investigation may include reviewing manufacturing records, conducting laboratory tests, and analyzing data.

• One example of an OOS investigation is when a pharmaceutical product fails to m...read more

Incident management process involves identifying, responding to, and resolving incidents to minimize their impact on business operations.

• The process starts with incident identification, where incidents are reported or detected.

• Once an incident is identified, it is logged and categorized based on its severity and impact.

• A response team is then assigned to investigate and resolve the incident.

• During the investigation, th...read more

Calibration of HPLC involves adjusting and verifying the accuracy and precision of the instrument.

• Calibration ensures that the HPLC system is performing accurately and reliably.

• It involves adjusting parameters such as flow rate, detector wavelength, and injection volume.

• Calibration standards of known concentration are used to verify the accuracy of the system.

• Precision is assessed by analyzing replicate injections of a...read more

Validation is the process of checking if something meets certain criteria. Types of validation include data validation, form validation, and email validation.

• Validation is the process of ensuring that something meets specific requirements or standards.

• Data validation involves checking the accuracy, completeness, and consistency of data.

• Form validation ensures that user input in web forms is correct and meets specified ...read more

To fix the specification limit for an unknown impurity in an API, conduct thorough analysis and consider regulatory guidelines.

• Perform comprehensive analysis of the impurity to determine its identity, properties, and potential risks

• Refer to regulatory guidelines and industry standards to establish acceptable limits for impurities

• Consider the impact of the impurity on the quality, safety, and efficacy of the API

• Collabor...read more

CPP parameters during filling stages refer to critical process parameters that need to be monitored and controlled to ensure product quality and consistency.

• CPPs during filling stages may include fill volume, fill speed, fill accuracy, and container closure integrity.

• Monitoring and controlling these parameters is essential to prevent issues such as underfilling or overfilling, which can impact product quality.

• Examples ...read more

I chose this organization and biopharma due to their strong experience, stability, and alignment with my career goals.

• I chose this organization because of their extensive experience in the biopharma industry.

• The organization has a proven track record of stability and success.

• I believe that working in the biopharma field will allow me to make a meaningful impact on patients' lives.

• The organization's mission and values a...read more