Bank of America Interview Questions and Answers

I have extensive technical knowledge of pharmaceutical production.

• I am familiar with Good Manufacturing Practices (GMP) and Quality Control (QC) procedures.

• I have experience in operating and maintaining production equipment such as tablet presses, capsule fillers, and packaging machines.

• I am knowledgeable in the formulation and compounding of pharmaceutical products.

• I am familiar with the various stages of pharmaceutical production, including raw material testing, in-process ...read more

Capsules and tablets are two common forms of medication. Capsules are gelatin shells filled with medication, while tablets are compressed powder.

• Capsules are available in two types: hard and soft gelatin capsules.

• Tablets can be categorized into four types: compressed, coated, chewable, and effervescent.

• Capsules are easier to swallow than tablets for some people.

• Tablets can be scored to make it easier to break them in half.

• Capsules are often used for oil-based or liquid medica...read more

The normal temperature for vaccines and sera varies depending on the type and manufacturer.

• Different vaccines and sera require different storage temperatures

• The recommended temperature range is usually indicated on the product label

• Most vaccines and sera need to be stored between 2-8°C

• Some vaccines, like the Pfizer-BioNTech COVID-19 vaccine, require ultra-cold storage at -70°C or below

• Exposure to temperatures outside the recommended range can affect the potency and efficacy o...read more

Packing in pharmaceutical refers to the process of packaging drugs in suitable containers. Types include primary, secondary, and tertiary packaging.

• Primary packaging involves the direct contact of the drug with the container, such as blister packs or vials.

• Secondary packaging includes the packaging of primary containers, such as cartons or boxes.

• Tertiary packaging involves the packaging of secondary containers for transportation and storage, such as pallets or shrink wrap.

• The...read more

Injection storage requires proper temperature, light, and humidity control.

• Injections should be stored in a cool, dry place.

• Temperature should be maintained between 2-8°C for most injections.

• Some injections may require freezing temperatures.

• Light exposure should be minimized.

• Humidity should be controlled to prevent moisture damage.

• Expired injections should be disposed of properly.

• Storage conditions should be monitored and recorded regularly.

Yes, quarantine rooms are designated areas for isolating individuals who may have been exposed to infectious diseases.

• Quarantine rooms are used to prevent the spread of infectious diseases.

• They are typically equipped with negative air pressure systems to prevent airborne transmission.

• Medical staff and visitors must wear protective gear when entering quarantine rooms.

• Examples of situations where quarantine rooms may be used include outbreaks of Ebola, SARS, or COVID-19.

Room temperature refers to the average temperature of a room or space.

• Room temperature is typically between 68-72 degrees Fahrenheit (20-22 degrees Celsius).

• It is important to maintain a consistent room temperature for certain products or processes.

• Room temperature can affect the comfort and productivity of individuals in a space.

• Temperature can be measured using a thermometer or thermostat.

• Factors such as humidity and air flow can also impact perceived room temperature.

GMP stands for Good Manufacturing Practice.

• GMP is a set of guidelines that ensure the quality and safety of pharmaceuticals, food, and medical devices.

• It covers all aspects of production, from raw materials to finished products.

• GMP requires documentation, quality control, and testing to ensure consistency and purity.

• Examples of GMP regulations include proper labeling, storage, and handling of products.

• GMP is enforced by regulatory agencies such as the FDA and EMA.