Steril Gene Life Sciences Production Supervisor Interview Questions and Answers

Q1. Basic question like about Myself, My college study and experience
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Q2. Technical knowledge about the study
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Q1. Totally technical questions relating to study and job.
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Q2. About the formulations I've studied.
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Q1. Why I want to join them?
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Q2. Salary expectations.
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Basic aptitude questions to check your awareness and activness

Q1. Technical test in which they ask your completed internship, education background, job roll related like if you apply for QC, production job , they ask you chromatography related questions etc.
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Q1. What is chromatography
Ans. 
Chromatography is a laboratory technique used to separate mixtures into their individual components.
• Chromatography involves passing a mixture through a stationary phase, which separates the components based on their different affinities for the stationary phase.

• The separated components are then detected and analyzed, allowing for identification and quantification of the individual substances.

• There are different types o...read more
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Q1. How much f0 value should be in autoclave?
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The f0 value in autoclave should typically be at least 8 to ensure proper sterilization.
• The f0 value is a measure of the lethality of a sterilization process, taking into account both time and temperature.

• A minimum f0 value of 8 is commonly recommended for autoclaves to ensure proper sterilization.

• Factors such as the type of load being sterilized and the desired level of sterility may influence the required f0 value.
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Q2. In tunnel depyrogenation zone vials how much time should be sterilization
Ans. 
The sterilization time in tunnel depyrogenation zone vials varies depending on the specific process and equipment used.
• Sterilization time can range from a few minutes to over an hour, depending on the temperature and method of sterilization.

• Factors such as the type of vials, the level of contamination, and the desired sterility assurance level also impact the sterilization time.

• For example, a tunnel depyrogenation proc...read more
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Q3. Why we are Doing VLT in autoclave
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Q4. Why we are doing In autoclave bowie test
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Autoclave Bowie test is conducted to ensure the sterilization process is effective and meets industry standards.
• To ensure that the autoclave is functioning properly and effectively sterilizing equipment

• To meet industry standards and regulations for sterilization processes

• To verify that the autoclave is killing all microorganisms and spores

• To prevent contamination and ensure the safety of patients and staff
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Q5. What will ensure in bowie test
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Ensuring proper testing procedures and accurate results in the bowie test.
• Properly calibrating equipment before conducting the test

• Following standardized testing protocols

• Ensuring the test samples are handled and stored correctly

• Regularly maintaining and servicing testing equipment

• Training staff on how to conduct the test accurately
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Q1. Normally environment related discussion and family background and what previous company information or future many time you stability can perform a in a company
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Q2. Production department realated questions and package discuss
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Q1. Which is pharmacovigilance
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Q1. Give me information about your company
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Q2. What is benifit for employees?
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Employee benefits include health insurance, retirement plans, paid time off, and professional development opportunities.
• Health insurance coverage for employees and their families

• Retirement plans such as 401(k) matching contributions

• Paid time off for vacation, sick leave, and holidays

• Professional development opportunities like training programs and tuition reimbursement

• Employee discounts on company products or services
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Q3. Why are you not selecting every peoples?
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Q4. What is your selection process?
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Q1. Appearance of interviewer
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Q2. Self introduction
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Q1. Difference between QA and QC Suspension , Emulsions , Solid Dosage Form , Semi solid dosage form, Parenteral formulation
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Q2. Difference between Qa and QC Suspension , emulsion , solid dosage form , Parenteral formulation , semi solid dosage form etc.
Ans. 
QA focuses on preventing defects while QC focuses on identifying and correcting defects.
• QA involves the process of ensuring that the product meets the required standards and specifications.

• QC involves the process of inspecting the product to identify any defects or deviations from the required standards.

• Examples of dosage forms include suspension, emulsion, solid dosage form, parenteral formulation, and semi-solid dosa...read more
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