TAPI
Pharmaceuticals
QualityControlTechnician(HPLC)
Neural analysis suggests this role is
optimal for entry candidates.
“Quality Control Technician (HPLC) at TAPI. Skills: HPLC analysis, Analytical testing, Laboratory operations. Perform analysis of raw materials. Perform analysis of intermediates”
Industry & Context.
Troubleshooting; Root cause analysis
Multi-shift environment, 24x7 audit readiness, Rotational shifts
What They're Looking For.
Must Have
B.Sc. / M.Sc. in Chemistry, B. Pharma, Minimum 3 to 4 years industrial experience
What You'll Do.
Perform analysis of raw materials
Perform analysis of intermediates
Perform analysis of finished products
Perform analysis of stability samples
Perform analysis of cleaning samples
Report results in analytical records
Report results in LIMS
Report results in QA documentation
Carry out routine operation of HPLC systems
Carry out calibration of HPLC systems
Carry out system suitability checks of HPLC systems
Carry out maintenance of HPLC systems
Troubleshoot chromatographic issues
Prepare mobile phases
Prepare standard solutions
Prepare test solutions
Ensure proper sampling
Ensure proper labeling
Handle samples with traceability
Maintain laboratory equipment
Maintain working areas
Maintain controlled environments
Support preparation of SOPs
Support review of SOPs
Support revision of SOPs
Support preparation of STPs
Support review of STPs
Support revision of STPs
Support preparation of analytical methods
Support review of analytical methods
Support revision of analytical methods
Monitor inventory of chemicals
Monitor inventory of reagents
Monitor inventory of columns
Monitor inventory of reference standards
Initiate LIR investigations
Initiate OOS investigations
Initiate OOT investigations
Assist in root cause analysis
Assist in CAPA implementation
Maintain data integrity
Manage electronic records
Perform secure data entry
Adhere to 21 CFR Part 11
Ensure 24x7 audit readiness
Support instrument qualification activities
Assist in analytical method validation studies
Assist in method transfer activities
Work in rotational shifts
Complete assigned training programs
Ensure compliance with CAPA actions
Maintain housekeeping standards
Maintain safety standards
How You'll Work.
Team & Collaboration
Coordination with cross-functional teams
Full Job Description
At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. We are looking for a proactive Quality Control (QC) Technician with strong hands-on experience in HPLC analysis, analytical testing, and laboratory operations. If you can operate in a multi-shift environment, maintain 24×7 audit readiness, and have experience in LIR/OOS/OOT investigations, instrument calibration, and GMP/GLP compliance, this opportunity in a pharmaceutical setup is ideal for you. 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 preparatio
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