TAPI hiring for Quality Control Jobs | Chemistry Candidates Apply Now
Looking for exciting Quality Control Jobs in the pharmaceutical industry? TAPI is hiring skilled candidates for QC laboratory operations at its Burhanpur facility. This opportunity is ideal for professionals searching for rewarding TAPI Careers and advanced Chemistry Jobs involving HPLC analysis, GMP compliance, laboratory operations, analytical testing, and pharmaceutical quality control activities in a globally recognized API manufacturing organization.
- Job Role: Quality Control Technician (HPLC)
- Location: Burhanpur
About the Company:
TAPI is one of the world’s leading suppliers of active pharmaceutical ingredients (APIs), serving major pharmaceutical companies across the globe. With over 80 years of industry expertise and operations across multiple countries, TAPI is known for innovation, quality, and scientific excellence. Through advanced manufacturing facilities and strong research capabilities, the company continues to create excellent TAPI Careers for professionals interested in pharmaceutical and analytical Chemistry Jobs.
Job Overview:
TAPI Careers has announced new Quality Control Jobs for the role of Quality Control Technician (HPLC) at its Burhanpur facility. The role involves analytical testing of raw materials, intermediates, finished products, and stability samples using HPLC techniques. Candidates applying for these Chemistry Jobs will work on laboratory operations, instrument calibration, analytical
documentation, LIMS handling, OOS investigations, GMP/GLP compliance, and audit readiness activities within a pharmaceutical manufacturing setup.Key Responsibilities
- Perform analysis of raw materials, intermediates, finished products, stability samples, and cleaning samples using HPLC as per approved monographs, test methods, and SOPs, ensuring accurate and timely result reporting in analytical records, LIMS, and QA documentation in line with data integrity requirements.
- Carry out routine operation, calibration, system suitability checks, and maintenance of HPLC systems, including troubleshooting of chromatographic issues to ensure consistent performance and compliance.
- Prepare mobile phases, standard solutions, and test samples; ensure proper sampling, labeling (approved/rejected), and handling of samples with full traceability and documentation.
- Maintain laboratory equipment, working areas, and controlled environments (sample rooms, chambers, etc.) in compliance with cGMP, GLP, and safety standards.
- Support preparation, review, and revision of SOPs, STPs, analytical methods, and other QC documentation in coordination with cross-functional teams.
- Monitor and maintain inventory of chemicals, reagents, columns, and reference standards with proper stock reconciliation.
- Initiate, investigate, and document LIR, OOS, OOT, and atypical/borderline results; assist in root cause analysis and implementation of CAPA.
- Maintain data integrity through proper electronic records management, secure data entry, and adherence to 21 CFR Part 11 requirements; ensure continuous 24×7 audit readiness by adhering to regulatory requirements.
- Support instrument qualification activities including IQ/OQ/PQ protocols and assist in analytical method validation studies and method transfer activities.
- Work in rotational shifts as required, complete all assigned training programs, ensure full compliance with CAPA-related actions, and maintain high standards of housekeeping and safety within the laboratory.
Qualifications
The ideal candidate will have:
- Education: B.Sc. / M.Sc. in Chemistry
- Experience: Minimum 3 to 4 years of industrial experience.
Candidates interested in building successful careers through Quality Control Jobs and long-term TAPI Careers can benefit greatly from this opportunity. These Chemistry Jobs provide valuable exposure to pharmaceutical quality systems, analytical instrumentation, laboratory compliance, and API manufacturing operations in an internationally recognized pharmaceutical organization.
