TAPI

API/Pharma

QualityControlTechnician

Gajraula, India FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for mid candidates.

The Brief

“Quality Control Technician at TAPI. Skills: Quality Control, GMP, GLP, Analytical Methods, Instrument Calibration, Deviation Investigations. Determining team priorities in accordance with the plant’s needs, while coordinating with the departmental manager. maintain the cleanliness of instrument and workplace with maintaining 5S”

What You'll Achieve.

deliver excellence; make a lasting impact on global health

Industry & Context.

API/Pharma
Problems you'll solve

solve problems; instrument troubleshooting; initiating investigations for deviations such as LIR, OOT, and OOS

Eligibility Requirements

adhere to the PPE requirement

What They're Looking For.

Must Have

Solid understanding of Quality Control procedures, knowledge of GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices), Good understanding of Autotitrator, Particle size analyzer, Polarimeter, Karl Fischer, UV-Vis, FTIR, pH meter & analytical balance, & Understanding of GXP, GLP & Safety, Ability to handle instrument troubleshooting and follow documentation protocols

What You'll Do.

Determining team priorities in accordance with the plant’s needs

while coordinating with the departmental manager

maintain the cleanliness of instrument and workplace with maintaining 5S

An active participant in scientific / development activities such as validation process

development of basic analytical methods etc.

GDP & ALCOA++ in the laboratory and safety guidelines

maintaining logbooks for all instrument usage

sampling of raw materials (RM)

Intermediate and cleaning as per applicable SOPs

preparation & standardization of volumetric/regents /indicator solutions

performing various wet analysis as per monograph and SOP’s with accurate documentation and timely reported results into LIMS system

Perform Technology transfer of PSD Analysis

Take care of online documentation and report the results

calibration / verification of instruments

initiating investigations for deviations such as LIR

and OOS as when observed

Ensure proper management

and storage of Primary standards

and Chemicals as per SOP requirements

Participate in Safety Promotion activities

mock drills & Safety Trainings

Follow safety procedures

protocols and adhere to the PPE requirement

Ensure non-routine activities are executed through the work permit system

How You'll Work.

Team & Collaboration

coordinating with the departmental manager; An active participant in scientific / development activities; Participate in Safety Promotion activities, mock drills & Safety Trainings

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’re seeking a detail-oriented and technically skilled professional to take on the role of QC Technician at our cutting-edge manufacturing facility in Gajraula. 📌 Key Responsibilities: 1. Determining team priorities in accordance with the plant’s needs, while coordinating with the departmental manager. 2. Responsible to maintain the cleanliness of instrument and workplace with maintaining 5S. 3. An active participant in scientific / development activities such as validation process, development of basic analytical methods etc. 4. Follow-up the cGMP, GLP, GDP & ALCOA++ in the laboratory and safety guidelines. 5. Responsible for maintaining logbooks for all instrument usage. 6. Responsible for sampling of raw materials (RM), finished goods (FG), Intermediate and cleaning as per applicable SOPs. 7. Responsible for preparation & standardization of volumetric/regents /indicator solutions. 8. Responsible for performing various wet analysis as per monograph and SOP’s with accurate documentation and timely reported results into LIMS system. 9. Perform Technology transfer of PSD Analysis. 10. Take care of online documentation and report the results. 11. Responsible for calibration / verification of instruments. 12. Responsible for initiating investigations for deviations such as LIR, OOT

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