Quality Control

Tanvesta solutions

2 - 8 years

0 Lacs

tirupati andhra pradesh

Posted:23 hours ago| Platform: Shine logo

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Skills Required

quality control gmp glp usfda mhra hplc analysis dosage forms 10key typing

Work Mode

On-site

Job Type

Full Time

Job Description

As a member of the team, you will be responsible for: - Conducting HPLC analysis of Solid Orals and Nasal products - Hands-on experience in Quality Control activities related to Raw Materials, Packing, In Process, and Finished Products - Ensuring compliance with GMP/GLP practices Qualifications required for this role: - Bachelor's or Master's degree in Pharmacy or Science - 3-8 years of relevant experience - Immediate joiners are preferred Additional details of the company: You will have the opportunity to work in a fully automated, world-class manufacturing facility. You will be involved in working with diverse dosage forms in a multi-product environment. Additionally, you will receive attractive attendance bonuses, special allowances, and unparalleled opportunities for learning and growth. Please note that this is a full-time position with benefits such as Provident Fund, yearly bonus, and day shift schedule. The ability to commute or relocate to Tirupati, Andhra Pradesh is required for this role. If you meet the qualifications and are ready to join immediately, we encourage you to apply. The application deadline for this position is 14/07/2025.,

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Quality Control