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Open nowPosted 36 days ago

Quality Control Technician (HPLC)

TAPI36 open roles

Where
Gajraula, Uttar Pradesh, India
Work mode
On site
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Your applicationOpen nowQuality Control Technician (HPLC)TAPI · Gajraula, Uttar Pradesh, India

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

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The clock on this job

Early applications get read.

11.8% of postings close within 7 days. Measured by our own scanner across the market. TAPI postings stay open a median of 7 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.4%3 days
  3. 11.8%7 days
  4. 18.6%14 days
  5. 35.6%30 days
  6. 45.1%60 days
This job: posted 36 days ago

TAPI median: 7 days open

The posting

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

We’re seeking a detail-oriented and technically skilled professional to take on the role of QC Technician at our cutting-edge manufacturing facility. This role is critical to ensuring the integrity, compliance, and reliability of our stability testing and analytical operations.

📌 Key Responsibilities:

  1. Analysis of stability samples, Finish Product samples & working standard qualification activity as per the defined procedure & monograph.
  2. Deep knowledge about the HPLC, GC, KF, Auto titrator, Vacuum open operation procedure as well as troubleshooting by following the GLP practices.
  3. Maintaining a system of methods and specification for all materials and products.
  4. Data filling and maintaining the logbooks, certificate, stability report and stability data in archive.
  5. To initiate the LIR / OOS if any procedural gap related with SOP / monograph during routine activity.
  6. Qualifications of all analytical instruments should be maintained in stability Section.
  7. Follow the defined safety procedure during day-to-day activity in laboratory.

🛠 Minimum Required Skills:

  • Solid understanding of Quality Control procedures.
  • Strong knowledge of GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices).
  • Ability to handle instrument troubleshooting and follow documentation protocols.

Qualifications

The candidate must have:

Experience Level: 3-6 Years

Industry Experience: API/Pharma Experience is required

Qualification: M.Sc. in 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.

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