Quality Control Analyst Recruitment – MSc Chemistry Apply
Dont forget to check out possible interview questions for this job below
Teva Pharmaceuticals hiring msc chemistry candidates. Chemistry job opening 2023, Quality control analyst job opening 2023, QC job opening 2023, Chemistry QC job opening 2023, Chemistry job opening 2023, Intrested and eligible candidates may check out all the details on the same below:
Job Title: Quality Control Analyst I
Location: Chennai, India, 600113
Company: Teva Pharmaceuticals
Job Id: 49579
Eligbility Criteria:
M.Sc., (Chemistry) with 5 to 10 years of experience.
Good communication skill.
Possess a pro-active, dynamic and flexible approach
How you’ll spend your day
- Performing Stability analysis and review of documents.
- Performing Method transfer/ Method Validation
- Calibration and validation of instruments / equipment’s.
- Preparation of Method Transfer Protocols (MTP), Method Transfer Report (MTR), Method of analysis (MTH), Test Data Sheet (TDS) for Stability Analysis and Method transfer /
- Validation any document related to stability analysis, method transfer / method
- validation in compliance with current guidelines.
- Preparation of departmental SOP’s in compliance with current guidelines.
- Preparation of validation protocols in compliance with current guidelines.
- Entry of stability sample results in LIMS.
- Handling of LSCMS Software.
Possible Interview Questions:
- Can you explain your experience in stability analysis and document review? Answer: Yes, I have 5 to 10 years of experience in stability analysis and document review. During this time, I have been responsible for performing stability analysis, reviewing documents, and ensuring compliance with current guidelines. I have a thorough understanding of the protocols and procedures involved in stability analysis and have successfully executed these tasks in my previous role.
- How familiar are you with method transfer and method validation processes? Answer: I am well-versed in both method transfer and method validation processes. I have hands-on experience in performing method transfers and method validations, ensuring the accuracy and reliability of analytical methods. I have prepared Method Transfer Protocols (MTP), Method Transfer Reports (MTR), and other relevant documents in compliance with current guidelines.
- Can you discuss your experience in calibration and validation of instruments/equipment? Answer: Throughout my career, I have actively participated in the calibration and validation of instruments and equipment used in the laboratory. I am experienced in performing calibration activities, ensuring the accuracy and precision of measurements. Additionally, I have executed validation protocols to establish the reliability and performance of instruments/equipment.
- How have you ensured compliance with guidelines while preparing departmental SOPs and validation protocols? Answer: Ensuring compliance with guidelines is crucial in my role. While preparing departmental SOPs and validation protocols, I meticulously follow the current guidelines and regulations. I conduct thorough research, review existing SOPs and protocols, and consult relevant references to ensure that the documents are accurate, up-to-date, and compliant with industry standards.
- Can you describe your experience with LIMS and handling LSCMS software? Answer: I have extensive experience in working with Laboratory Information Management Systems (LIMS) and handling LSCMS software. I am proficient in entering stability sample results in LIMS, maintaining accurate records, and generating reports. I have also gained expertise in utilizing LSCMS software for data analysis and interpretation.
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