QC Officer Job BSV – Bharat Serums And Vaccines MSc Biotech Job
QC Officer Job BSV – Bharat Serums And Vaccines MSc Biotech Job. BSV job opening for MSc Biotechnology candidates. MSc job openings. Interested and eligible applicants can check out all of the details on the same below
Possible interview questions are posted below
QUALITY CONTROL OFFICER
Experience: From 0 to 1 year(s) of experience
Location: Mumbai (All Areas) ( Ambernath), Ambernath
About the job
Job Description
Accountabilities and Responsibilities:
- To maintain the workplace neat and tidy and follow GLP requirements religiously
- To perform analysis of Finished Products Raw Material, In process and Stability Study of Biotechnological samples.
- To be responsible for sample management.
- Raw material sampling as per sampling SOP
- To prepare and standardize wherever required bench reagents, indicators, volumetric solutions, and buffer solutions as per need and record the data
- To record the raw data of analysis in respective protocols and review them before submission for verification to Superior/ Head of the department
- To follow SOPS related to activities and operations
- To perform and record the calibrations of instruments as per schedule.
- Preparation of Working Standards, volumetric samples and maintain the documents of the same.
- To monitor and record temperature and humidity of QC department.
- To report OOS results and deviations occurred during testing and operations to Head QC for performing investigation. Investigation and reporting of any “OOS observed in QC along with Section Head and Manager QC.
Competencies:
- Good communication skills
- Good knowledge of Biotechnology.
Key Skills
- SDS-Page
- RT-PCR
- Quality control
- UV Spectrophotometer
- ELISA
- biotechnology
- sampling
- glp
- Gmp Compliance
- qc
- instruments
- sop
- calibration
- HPLC
Skills that are made bold are preferred key skills
Education
- MS/M.Sc(Science) in Biotechnology
Role: Other
Salary: Not Disclosed by Recruiter
Industry: Pharmaceutical & Life Sciences
Department: Other
Role Category: Other
Employment Type: Full-Time, Permanent
Possible interview questions:
- Question: Can you explain your experience with GLP (Good Laboratory Practice) requirements and how you have ensured compliance in your previous role? Answer: In my previous role, I was responsible for maintaining the workplace neat and tidy and religiously following GLP requirements. I ensured proper documentation, adherence to SOPs, and recording of raw data in respective protocols. I also conducted regular calibrations of instruments as per the schedule to maintain accuracy and precision in the testing process.
- Question: How familiar are you with performing analysis of Finished Products, Raw Material, and In-process samples in a biotechnological setting? Answer: I have gained hands-on experience in performing analysis of Finished Products, Raw Material, and In-process samples during my academic pursuits and internships. I am well-versed with techniques like SDS-Page, RT-PCR, and UV Spectrophotometer, which are crucial for quality control in a biotechnological laboratory.
- Question: How do you handle sample management, especially in terms of raw material sampling and maintaining records as per SOPs? Answer: I approach sample management with precision and attention to detail. I follow the sampling SOPs diligently to ensure accurate representation of raw materials. Additionally, I maintain comprehensive records, recording the data and results in an organized manner for easy retrieval and verification.
- Question: Have you encountered any instances of Out of Specification (OOS) results during your previous testing and how did you handle them? Answer: Yes, I have encountered OOS results during my testing. In such cases, I promptly reported the deviations to the Head QC for further investigation. We collaborated with the Section Head and Manager QC to perform a thorough investigation to identify the root cause and take appropriate corrective actions to prevent recurrence.
- Question: Can you share an experience where you prepared and standardized bench reagents, volumetric solutions, or buffer solutions to meet specific testing requirements? Answer: During my academic lab work and internships, I have prepared and standardized bench reagents and buffer solutions to support various experiments. The process involved careful measurements, ensuring proper concentrations, and validating the solutions for use in specific analyses.
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Respected sir,
I am writing this email to apply for the position of QC and QA Executive in our company. I graduated from Ayya Nadar Janaki Ammal College (Autonomous), Sivakasi, with a Master’s degree. At CSIR-CECRI, I completed my M.Sc. dissertation work. I promise you my dedication and enthusiasm. I am hoping for a good answer to this application.
I am Tejasvini Sharadchandra Deore.i have completed my post graduation in biotechnology from RCP ACS College Shirpur.i am interested in QA,QC,& R&D departments.