TAPI

Pharmaceuticals

QualityControlTechnician(HPLC)

₹6–10L ~AI est. Malanpur, Madhya Pradesh, India FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for entry candidates.

The Brief

“Quality Control Technician (HPLC) at TAPI. Skills: HPLC analysis, Analytical testing, Laboratory operations. Perform analysis of raw materials. Perform analysis of intermediates”

Industry & Context.

Pharmaceuticals
Problems you'll solve

Troubleshooting; Root cause analysis

Eligibility Requirements

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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