Require a QC Lab in Bengaluru

TestHiring

Job Location:

Bengaluru - India

Monthly Salary: K 10 - 10

Experience Required: 2-5years

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

Perform routine and specialized quality control tests on raw materials in-process samples and finished products using advanced analytical instruments (e.g. HPLC GC UV-Vis FTIR).
Maintain accurate and detailed records of all testing activities in compliance with SOPs and GxP standards.
Calibrate maintain and troubleshoot laboratory equipment to ensure optimal performance and data integrity.
Investigate and document deviations out-of-specification (OOS) results and non-conformances; collaborate with cross-functional teams to implement corrective and preventive actions (CAPA).
Support method validation verification and transfer activities in alignment with industry guidelines (e.g. ICH USP EP).
Ensure adherence to safety protocols environmental standards and regulatory requirements (ISO 17025 GLP etc.).
Participate in internal and external audits providing documentation and support as needed.
Contribute to continuous improvement initiatives by analyzing trends generating reports and recommending process enhancements.
Train and mentor junior lab personnel on best practices safety procedures and quality standards.

Requirements

Bachelors degree in Chemistry Biochemistry Chemical Engineering or a related scientific discipline.
25 years of hands-on experience in a QC laboratory within the technology pharmaceutical or semiconductor industry.
Proficiency in analytical techniques including HPLC GC UV-Vis FTIR and Karl Fischer titration.
Strong understanding of GMP GLP ISO 17025 and other relevant quality systems.
Experience with LIMS (Laboratory Information Management Systems) and electronic data management.
Excellent attention to detail organizational skills and ability to work independently and in a team environment.
Ability to interpret technical documentation write clear reports and communicate findings effectively.
Familiarity with CAPA root cause analysis and risk assessment tools (e.g. FMEA 5 Whys).
Willingness to work in a regulated environment with strict adherence to documentation and compliance standards.

Required Skills:

Career in software testing

Required Education:

(CSE IT)

Perform routine and specialized quality control tests on raw materials in-process samples and finished products using advanced analytical instruments (e.g. HPLC GC UV-Vis FTIR).Maintain accurate and detailed records of all testing activities in compliance with SOPs and GxP standards.Calibrate mainta...

Perform routine and specialized quality control tests on raw materials in-process samples and finished products using advanced analytical instruments (e.g. HPLC GC UV-Vis FTIR).
Maintain accurate and detailed records of all testing activities in compliance with SOPs and GxP standards.
Calibrate maintain and troubleshoot laboratory equipment to ensure optimal performance and data integrity.
Investigate and document deviations out-of-specification (OOS) results and non-conformances; collaborate with cross-functional teams to implement corrective and preventive actions (CAPA).
Support method validation verification and transfer activities in alignment with industry guidelines (e.g. ICH USP EP).
Ensure adherence to safety protocols environmental standards and regulatory requirements (ISO 17025 GLP etc.).
Participate in internal and external audits providing documentation and support as needed.
Contribute to continuous improvement initiatives by analyzing trends generating reports and recommending process enhancements.
Train and mentor junior lab personnel on best practices safety procedures and quality standards.

Requirements

Bachelors degree in Chemistry Biochemistry Chemical Engineering or a related scientific discipline.
25 years of hands-on experience in a QC laboratory within the technology pharmaceutical or semiconductor industry.
Proficiency in analytical techniques including HPLC GC UV-Vis FTIR and Karl Fischer titration.
Strong understanding of GMP GLP ISO 17025 and other relevant quality systems.
Experience with LIMS (Laboratory Information Management Systems) and electronic data management.
Excellent attention to detail organizational skills and ability to work independently and in a team environment.
Ability to interpret technical documentation write clear reports and communicate findings effectively.
Familiarity with CAPA root cause analysis and risk assessment tools (e.g. FMEA 5 Whys).
Willingness to work in a regulated environment with strict adherence to documentation and compliance standards.

Required Skills:

Career in software testing

Required Education:

(CSE IT)