Torrent Pharmaceutical Limited- Walk-In Interview for Quality Control -Formulation On 26th Nov’ 2023

Torrent Pharmaceutical Limited- Walk-In Interview for Quality Control -Formulation On 26th Nov’ 2023

Torrent Pharma, the flagship company of Torrent Group, is one leading pharma companies in the country. Torrent is all poised to spread wings across globe with strong technical capabilities and international accreditations.

Post : Executive / Technical Assistant

Department : Quality Control (Formulation)
Criteria : B.Pharm / MSC 2 to 7 years of relevant experience

Skills
• Exposure of analysis for Finished Product, Stability Samples & Raw Materials.
• Having sound knowledge of Operation, Troubleshooting of QC Instruments & Investigation of OOS/OOT/Deviation. (e g HPLC, GC, UV, GCMS, LCMS, FTIR, Polarimeter, UV Spectrophotometer, KF, Apparatus)
• Having Knowledge of Analytical Method Validation, Verification & Method Transfer. Having skill for data Interpretation, troubleshooting.
• Exposure of QC compliance and GLP activities.

Others : Pharma knowledge of Solid orals & Quality process. USFDA, MHRA, ANVISA & Other regulatory exposure is preferred including ICH guidelines.

Job Location : Baddi, Himachal Pradesh

Walk in Interview
Date : 26th November, 2023
Time : 9:00 am to 2:00 pm
Venue : Torrent Pharmaceuticals Ltd, Near Baddi University, Village – Bhud, Makhnu Majra, Tehsil- Baddi, Distt – Solan, HP-173205

Please carry your latest resume, salary slips, passport size photograph.

Job Category: pharma
Job Type: Full Time
Job Location: Baddi (H.P

Apply for this position

Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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