Nasense Labs walk-in interview for Quality Control department on 9th May – 18th May 2024

Nasense Labs walk-in interview for Quality Control department on 9th May – 18th May 2024

We are Nasense Labs, a forward-thinking company involved in the comprehensive production of Fine Chemicals and Semio Chemicals. Our Manufacturing Base is located in Hyderabad, India, and is backed by a well-equipped R&D facility, which includes a Pilot Plant and Analytical Development & Safety Labs.

Greetings from Nasense Labs Private Limited!

We are conducting walk-in interview for Chemist roles in Quality Control department on 9th May – 18th May 2024 at Hyderabad.

Department: Quality Control

Designation: Chemist

Qualification: MS/M.Sc(Science) in Chemistry

Experience: 2 – 5 years

Role & responsibilities

1.Sampling of Raw Material, In-process Packing material.

2.Preparation of specifications, standard test procedures (STP’s) and SOP’s.

Related Jobs  Abbott Walk-in interview for BSc, B Pharm, M Pharm Freshers on 11th May 2024

3. Handling Of the stability study.

4.Experience in Wet Analysis and HPLC, GC Instrumentation.

Preferred candidate profile: Required keen experience in Wet analysis, HPLC , GC and Instrumentation.

Work Location: Hyderabad

Date & Time: 9th May – 18th May 2024, 9.30 AM – 4.30 PM
Venue: Plot Numbers 24 & 25, SV Cooperative Industrial Estate, Quthubullapur, IDA Jeedimetla, Hyderabad, Telangana – 500055.
Contact – Chandra sekhar ( 8977003893 )

Perks and benefits

Best in industry along with Statutory benefits

Job Category: pharma
Job Type: Full Time
Job Location: Hyderabad. T.S

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

Check Also

MICROBIOLOGICAL CONTROL FOR EXCIPIENTS, DRUG PRODUCT AND DRUG SUBSTANCE

MICROBIOLOGICAL CONTROL FOR EXCIPIENTS, DRUG PRODUCT AND DRUG SUBSTANCE PURPOSE: To describe microbiological test controls …