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:
Determining team priorities in accordance with the plant’s needs, while coordinating with the departmental manager.
Responsible to 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.
Follow-up the cGMP, GLP, GDP & ALCOA++ in the laboratory and safety guidelines.
Responsible for maintaining logbooks for all instrument usage.
Responsible for sampling of raw materials (RM), finished goods (FG), Intermediate and cleaning as per applicable SOPs.
Responsible for preparation & standardization of volumetric/regents /indicator solutions.
Responsible for 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.
Responsible for calibration / verification of instruments.
Responsible for initiating investigations for deviations such as LIR, OOT, and OOS as when observed.
Ensure proper management, usage record, and storage of Primary standards, Reagents, Volumetric Solution, indicators, and Chemicals as per SOP requirements.
Report unsafe acts, conditions, near misses, and events.
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
🛠
Minimum Required Skills:
Solid understanding of
Quality Control procedures.
Strong 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.
The ideal candidate must have:
Experience Level:
3-6 Years
Industry Experience:
API/Pharma Experience is required
Qualification:
M.Sc. in Chemistry
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!
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 the industry. We look forward to receiving your application, 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.
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.
