Karnataka Antibiotics & Pharmaceuticals Limited QC Analyst Opportunity For MSc Biotech & Microbiology Candidates

KAPL Vacancies 2023 – QC Analyst For Biotech & Microbiology

KAPL Vacancies 2023 – QC Analyst For Biotech & Microbiology. Karnataka Antibiotics & Pharmaceuticals Limited (KAPL) Biotech and Microbiology QC Analyst job openings. Interested and eligible applicants can check out all of the details on the same below

Possible Interview Questions for the role of Quality Control Analyst at KAPL are posted below

This job expires in

KARNATAKA ANTIBIOTICS & PHARMACEUTICALS LIMITED
[ A GOVERNMENT OF INDIA ENTERPRISE] Registered & Corporate Office: KAPL House, Arka The Business Centre
Plot No. 37, Site No. 31/4, NTTF Main Road, 2nd Phase, Peenya Industrial Area,
Bengaluru – 560 058 Phone No.080-23571590
Fax. : 091(080)23371350. Website – www.kaplindia.com

Name of the post – Analyst-III –Quality Control.

No. of post – 1 post

Department – Quality Control

Age – Below 30 Years

Job Location – Dharwad

How to Apply –

The candidate is working in Govt. Department / Public Sector Undertaking are required to forward their application through the proper channel / produce a No Objection Certificate.

Relaxation in eligibility criteria may be considered for the above post for exceptionally deserving candidates.

Interested candidates who fulfil the requirements may send their

duly filled-in application as per the format [Application For Employment] available in our Company’s website : www.kaplindia.com along with the relevant testimonials to reach us on or before 12.06.2023 to Dy. General Manager – HRD.

Note: Candidates applying for the above post should write “Application for the post of…………………………” on the top of the envelope.

Salary Package – Monthly Gross Salary Around Rs. 29000/-[ Basic+VDA+HRA]

Qualification: M.Sc., Microbiology /Biotechnology or relevant qualification

Experience: Minimum -2-3 years of experience in relevant field.

Job Descriptions

• Preparation of Media for Water analysis, Microbial limit test, Preservative efficacy test, Antibiotic Assay etc.
• Microbial Limit Test for Ayurvedic Raw Materials, In-process Sample and Finished Products.
• Knowledge of handling and calibration of Instruments like Autoclave, Laminar Air Flow, Incubators, Microscope, Weighing Balance, pH meter, Colony Counter Fogger machine etc.,
• Culture and Staining Techniques of Microbes. Identification of specified pathogens.
• Investigation out of specifications, deviations and contamination events.
• GLP and documentation, laboratory facility maintenance.

Click here to download the application format 

View Notification 

Possible Interview Questions for the role of Quality Control Analyst at KAPL:

1. Can you explain your experience in preparing media for water analysis and conducting microbial limit tests? What specific techniques and methods did you employ? Answer: In my previous role, I have prepared various types of media for water analysis, including agar plates and broths, and conducted microbial limit tests using appropriate dilution techniques and plating methods. I followed standard operating procedures and ensured accurate and reliable results by maintaining aseptic conditions throughout the process.
2. How familiar are you with handling and calibrating laboratory instruments such as autoclaves, laminar airflow cabinets, incubators, microscopes, weighing balances, pH meters, colony counters, and fogger machines? Can you share any challenges you faced while working with these instruments? Answer: I have extensive experience in handling and calibrating a wide range of laboratory instruments. For example, I regularly calibrated autoclaves to ensure proper sterilization, maintained laminar airflow cabinets for contamination-free work, and performed routine checks on incubators and microscopes. One challenge I faced was troubleshooting pH meter readings due to electrode calibration issues, but I quickly resolved it by recalibrating the electrode.
3. Can you describe your approach to culture and staining techniques of microbes and the identification of specified pathogens? Have you worked with any specific staining methods or diagnostic tests? Answer: In my previous positions, I have employed various culture techniques, including streaking, pour plate, and spread plate methods, to isolate and grow different microorganisms. I have also performed Gram staining, acid-fast staining, and special staining techniques to identify bacteria, fungi, and other pathogens. Additionally, I have used diagnostic tests such as PCR and ELISA for the detection and identification of specific pathogens.
4. How have you handled situations involving out-of-specification results, deviations, or contamination events in the laboratory? Can you share an example and describe your problem-solving approach? Answer: In my experience, encountering out-of-specification results or deviations is not uncommon in a laboratory setting. When faced with such situations, I immediately initiate an investigation by thoroughly reviewing the experimental procedures, data, and sample handling. I collaborate with the team to identify potential causes, perform root cause analysis, and take appropriate corrective actions to prevent reoccurrence. For instance, I once discovered a contamination event during a microbial limit test, and I promptly isolated the contaminated sample, sterilized the affected area, and implemented stricter aseptic protocols to prevent future incidents.
5. How familiar are you with Good Laboratory Practices (GLP) and documentation requirements in a quality control setting? Can you provide examples of your experience in maintaining accurate records and ensuring compliance with regulatory standards? Answer: I am well-versed in GLP guidelines and the importance of maintaining accurate documentation. I have consistently followed GLP principles in my work by documenting all relevant information, including sample details, test procedures, observations, and results, in laboratory notebooks or electronic systems. I have also ensured compliance with regulatory standards by regularly reviewing and updating standard operating procedures, performing equipment qualifications, and participating in internal and external audits to verify adherence to quality and safety standards.

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