Quality Control - Executive / Sr. Executive Tanvesta solutions
Tanvesta solutions
Office Location
Full Time
Experience: 2 - 2 years required
Pay:
Salary Information not included
Type: Full Time
Location: Andhra Pradesh
Skills: GMP, HPLC Analysis, QC activities, GLP Practices
About Tanvesta Solutions
Job Description
You should possess a Bachelor's or Master's degree in Pharmacy or Science with 3-8 years of experience. Immediate joiners are preferred for this role. As a part of your role, you will be responsible for conducting HPLC analysis of solid orals/nasal products, handling QC activities related to Raw Materials, Packing, In Process, and Finished Products, and ensuring compliance with GMP/GLP Practices. The ideal candidate should have 2-8 years of experience and should have prior experience working in regulated plants approved by USFDA/MHRA. Working in this position will provide you with the opportunity to work in a fully automated world-class manufacturing facility, handle diverse dosage forms in a multi-product environment, receive attractive attendance bonuses and special allowances, and access unmatched opportunities for learning and professional growth. This is a full-time position with benefits including Provident Fund, day shifts, yearly bonus, and the requirement to commute or relocate to Tirupati, Andhra Pradesh. If you are ready to join immediately, have a minimum of 3 years of experience in 10-key typing, and are willing to work in person, we encourage you to apply before the deadline on 14/07/2025.,