Quality Control Analyst (Wet Lab)

Posted 5 Days Ago
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Gajraula, Amroha, Uttar Pradesh, IND
In-Office
Senior level
Pharmaceutical • Chemical • Manufacturing
The Role
Performs wet chemistry quality control testing for active pharmaceutical ingredients in a GMP-regulated laboratory. Responsibilities include analytical balance and pH calibration, laboratory temperature monitoring, sample and solution preparation, titration, assay, particle size, loss-on-drying, UV, FTIR, and polarimeter testing. The role requires compliance with cGMP, ICH, FDA, EU GMP, WHO GMP, and data integrity requirements, along with accurate documentation and instrument handling.
Summary Generated by Built In
Company 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.

Job Description

This role offers an excellent opportunity for a quality professional to build expertise in API laboratory operations, wet chemistry testing, GMP compliance, and analytical instrumentation while working in a highly regulated pharmaceutical environment. The position provides strong technical learning, cross-functional exposure, and a clear pathway for advancement into senior analytical and quality leadership roles.

1.Daily calibration of analytical balance.

2.Daily pH calibration.

3.Daily temprature monitroing of laboratory

4.Wet chemical analysis with different instrument such as UV, FTIR, BDTD, ROI, LOD, assay by Titration & PSD.

A. Laboratory Technical Skills: Sample Preparation, Weighing and dispensing of chemicals

Solution preparation and dilution techniques,Standard and reagent preparation

pH adjustment and buffer preparation, Filtration and extraction techniques.

B. Instrument Handling: UV-Visible Spectrophotometer, FTIR (Fourier Transform Infrared Spectroscopy), Particle Size Analyzer, Polarimeter.

C. GMP & Compliance Knowledge: (Regulatory Requirements) Current Good Manufacturing Practices (cGMP), ICH Guidelines., USFDA Regulations, EU GMP Requirements, WHO GMP Guidelines, Data Integrity Compliance (ALCOA+ principles).

Qualifications

Experience Required: 7-10 Years

Qualification : Msc-Chemistry

Additional Information

Make Your Mark with TAPI

Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Our Commitment

At TAPI, we believe great talent comes from many backgrounds and experiences. As an equal opportunity employer, we are committed to building a diverse, inclusive, and supportive workplace where everyone can belong, contribute, and grow. We encourage applications from all individuals who share our curiosity, ambition, and values.

Skills Required

  • 7-10 years of experience in pharmaceutical quality control or analytical laboratory operations
  • MSc in Chemistry
  • Experience with wet chemical analysis, titration, assay, particle size, loss on drying, and related laboratory testing
  • Experience operating UV-Visible spectrophotometers, FTIR, particle size analyzers, and polarimeters
  • Knowledge of cGMP, ICH guidelines, USFDA regulations, EU GMP requirements, and WHO GMP guidelines
  • Knowledge of data integrity and ALCOA+ principles
  • Laboratory sample preparation, chemical weighing, solution dilution, reagent preparation, pH adjustment, filtration, and extraction skills
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The Company
4,100 Employees

What We Do

TAPI is a global leader in the development and manufacturing of active pharmaceutical ingredients (APIs), building blocks, and key starting materials (KSMs). The company provides one of the industry's most comprehensive API portfolios and customized CDMO services, utilizing extensive expertise and innovation to drive pharmaceutical progress and ensure the delivery of high-quality, safe and effective medications to patients worldwide.

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