Production Officer / Production executive in pharmaceutical industry I 55 Interview questions

Production Officer / Production executive in pharmaceutical industry I 55 Interview questions and answers
-----------------------------------------------------------------------------------------------
Go to below playlists and search for a topic you want:
1. QMS - Quality Management System in Pharmaceutical industry : • QMS - Quality Manageme...
2. QA- Quality assurance in Pharmaceutical industry. : • QA- Quality assurance ...
3. QC - Quality Control in Pharmaceutical industry : • QC - Quality Control i...
4. OSD - Tablet Manufacturing in Pharmaceutical industry : • OSD - Tablet Manufactu...
5. Injectable processing - Injectable processing or Sterile dosage formulation : • Injectable processing ...
-----------------------------------------------------------------------------------------------
Questions covered:
Q. Introduce yourself / tell me something about you.
Q. Tell me about your industrial experience ?
Q. What is your job role in current organization ?
Q. What is the role of production officer in pharmaceutical industry ?
Q. Which are the important guidelines that are referred in pharmaceutical industry ?
Q. : What are good documentation practices (GDP) in the pharmaceutical industry?
Q. : What are Good Manufacturing Practices (GMP) in the pharmaceutical industry?
Q. : What is change control ?
Q.: What are the types of change control?
Q. :What is Deviation?
Q. What are the categories / classifications of deviation?
Q.: How do you classify deviations?
Q. : What is difference between Corrective action and preventive action?
Q. What steps do you take to prevent cross-contamination in pharmaceutical production?
Q. What is ALCOA ++?
Q. When we should perform Equipment Qualification ?
Q. What is Area Qualification in Pharmaceutical Industry?
Q. : What is calibration, and why is it essential in the pharmaceutical industry?
Q. What are the main parameters that require calibration in the pharmaceutical industry?
Q. What is limit for airborne particle concentration i.e. NVPC in Grade A, B, C and D ?
Q. Which guidelines are commonly referred for clean room in pharmaceutical industry ?
Q.: What is cleaning validation ?
Q. : When we should perform cleaning validation ?
Q.: Why three cycles are considered during validation / Qualification run?
Q. What is difference between cleaning and disinfection
Q. What is difference between Sanitization and sterilization ?
Q.: What is the difference between Sterile and Aseptic area ?
Q. What does HEPA stand for, and what is its primary function?
Q. What is the efficiency of a HEPA filter?
Q.: Why 0.2 micron filter is used for aseptic filtration in the pharmaceutical industry ?
Q.What is Electronic signature ?
Q. Why human error evaluation and control is important in pharmaceutical industry?
Q. What are the five common reasons for human errors in pharmaceutical industry?
Q. What is HVAC qualification in the pharmaceutical industry?
Q: What are the critical environmental parameters monitored during batch manufacturing process?
Q. Which QMS elements trigger investigation ?
Q. What are the key elements of Investigation report ?
Q : What is pH ?
Q : Which are the simple investigation tools commonly used in Pharmaceutical industry?
Q : Which are the advance investigation tools commonly used in Pharmaceutical industry?
Q : What are the reasons for lower assay in pharmaceutical industry ?
Q : Which are the five reasons for using SS 316 as product contact part in pharmaceutical industry ?
Q : Which are the five reasons for using Epoxy in pharmaceutical industry.
Q. : What are nitrosamine impurities and why are they a concern in the pharmaceutical industry?
Q: What is the significance of conducting stability studies for pharmaceutical products?
Q: What is the role of Standard Operating Procedures (SOPs) in pharmaceutical industry?
Q: How is data integrity ensured in the pharmaceutical industry?
Q: What is the role of internal audits in pharmaceutical industry ?
Q: What is the role of Training in pharmaceutical industry ?
Q. What is concept of RFT
Q. : What is Technology transfer in pharmaceutical industry ?
Q. What is temperature mapping in the pharmaceutical industry?
Q : What is USFDA expectation about training in Pharmaceutical industry ?
Q. What are the weighing balance calibration parameters ?
Q. Which are the important regulatory authorities for pharmaceutical industry ?
-----------------------------------------------------------------------------------------------
Copyright disclaimer:
“Any illegal reproduction of this content will result in immediate legal action.”

[@sukanyamodak306]

Very informative 🙌💯

[@PharmGrow]

Thanks

[@jammulakshmanaraolakshmana5881]

Exllent

[@PharmGrow]

Thanks

[@senapathisainaidu2237]

Please provide the data of sterile filling and stoppering machine qualifications...and area qualifications

[@PharmGrow]

I have uploaded one video on area qualification. I will post dedicated video on sterile filling and syoppering machine

[@maheshkamble8071]

Sir
Please make a video on fbd and fbp topic ..???

[@PharmGrow]

I started working on this topic. You will get video very soon.