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3 Job openings at Bas Technologies
Pharma Analytical Validation Method

Nimrana, Rajasthan

0 years

INR 2.4 - 4.2 Lacs P.A.

On-site

Full Time

Plan, execute, and document analytical method validation (accuracy, precision, specificity, linearity, robustness, LOD/LOQ, etc.) for raw materials, in-process samples, finished products, and cleaning validation. Review and approve validation protocols and reports in compliance with ICH Q2(R1), USP, and other regulatory requirements. Ensure all AMV activities meet GMP, GLP, and cGMP guidelines. Coordinate with R&D, QA, and Production teams for smooth tech transfer and validation support. Troubleshoot analytical method issues and recommend improvements or revalidations when necessary. Maintain and calibrate analytical instruments (e.g., HPLC, GC, UV-Vis, FTIR). Prepare for and participate in regulatory inspections and internal audits. Train and mentor junior QC staff on method validation procedures and regulatory expectations. Ensure all documentation is complete, accurate, and archived as per SOPs. Job Location: Giloth (Neemrana Rajasthan) Experienced Only Required Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹35,000.00 per month Benefits: Commuter assistance Food provided Schedule: Day shift Supplemental Pay: Overtime pay Yearly bonus Work Location: In person

Pharma Analytical Validation Method

Nīmrāna

0 years

INR 2.4 - 4.2 Lacs P.A.

On-site

Full Time

Plan, execute, and document analytical method validation (accuracy, precision, specificity, linearity, robustness, LOD/LOQ, etc.) for raw materials, in-process samples, finished products, and cleaning validation. Review and approve validation protocols and reports in compliance with ICH Q2(R1), USP, and other regulatory requirements. Ensure all AMV activities meet GMP, GLP, and cGMP guidelines. Coordinate with R&D, QA, and Production teams for smooth tech transfer and validation support. Troubleshoot analytical method issues and recommend improvements or revalidations when necessary. Maintain and calibrate analytical instruments (e.g., HPLC, GC, UV-Vis, FTIR). Prepare for and participate in regulatory inspections and internal audits. Train and mentor junior QC staff on method validation procedures and regulatory expectations. Ensure all documentation is complete, accurate, and archived as per SOPs. Job Location: Giloth (Neemrana Rajasthan) Experienced Only Required Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹35,000.00 per month Benefits: Commuter assistance Food provided Schedule: Day shift Supplemental Pay: Overtime pay Yearly bonus Work Location: In person

Pharma Analytical Validation Method

neemrana, rajasthan

3 - 7 years

INR Not disclosed

On-site

Full Time

You will be responsible for planning, executing, and documenting analytical method validation activities for raw materials, in-process samples, finished products, and cleaning validation. This includes assessing accuracy, precision, specificity, linearity, robustness, LOD/LOQ, and other parameters. You will review and approve validation protocols and reports in accordance with ICH Q2(R1), USP, and other regulatory standards to ensure compliance. Your role involves ensuring that all analytical method validation (AMV) activities adhere to GMP, GLP, and cGMP guidelines. Collaboration with R&D, QA, and Production teams is essential for seamless tech transfer and validation support. You will troubleshoot analytical method issues, propose enhancements, and recommend revalidations as needed. Maintenance and calibration of analytical instruments such as HPLC, GC, UV-Vis, and FTIR will be part of your responsibilities. In preparation for regulatory inspections and internal audits, you will participate in these processes. Additionally, you will play a key role in training and guiding junior QC staff on method validation procedures and regulatory expectations. It is crucial to ensure the completeness, accuracy, and proper archiving of all documentation as per standard operating procedures (SOPs). This position is based in Giloth, Neemrana, Rajasthan, and requires prior experience in a similar role. The job is full-time and permanent, offering benefits such as commuter assistance and provided meals. The work schedule is during day shifts with a yearly bonus component. The role necessitates on-site presence for work. If you meet the experience requirements and are adept at analytical method validation within a regulated environment, we invite you to apply for this challenging opportunity.,

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