R&D Center-AR&D-Senior Executive

PeopleStrong; Pashamylaram; On-site; INR 300,000 - 700,000; Full time

Job summary

Sekhmet Pharmaventures is hiring for a Senior Executive in the R&D center. You will perform hands-on HPLC, GC and physico-chemical analyses, including method development, validations and documentation to support regulatory filings.

Experience in LC-MS/GC-MS and knowledge of USP/EP/IP pharmacopeias are essential. This is a full-time, non-campus role based in India, South region, reporting to the R&D department.

Qualifications

• Hands-on experience with HPLC, GC and physico-chemical analysis (UV, IR, TLC) and titration including method development and routine analysis with good documentation practices.
• Hands-on experience with LC-MS/GC-MS including method development, validation and identification of unknown peaks with good documentation practices.
• Awareness of regulatory guidelines, including USP/EP/IP Pharmacopeias.

Responsibilities

• Conduct HPLC/GC and physico-chemical analyses with accurate documentation and data integrity.
• Develop and validate analytical methods including LC-MS/GC-MS and ensure regulatory compliance.

Skills

HPLC

Education

Post Graduate

M Pharma

Job description

• Sekhmet Pharmaventures>Optimus Drugs (P) Ltd>ODPL-R&D>R&D>A R & D>ODPL AR&D Common>2800801904

Posted On 02 Sep 2026

End Date 16 Sep 2026

Required Experience 2 - 5 years

Basic Section

No. Of Openings 1

Grade L6C

Designation Senior Executive

Campus/Non Campus Non Campus

Employment Type Full Time

Requisition Type Replacement

Median 300000 - 700000

Comp off OT Applicability Comp off & Overtime

TAT 30

Confidential No

Closing Date 16 Sep 2026

Organisational

Company Sekhmet Pharmaventures

Entity Optimus Drugs (P) Ltd

Department R&D

Sub- Department A R & D

Cost Centre 2800801904

Country India

Region South

Unit R&D Center

Skills

Skill

HPLC

Post Graduate

M Pharma

Working Language

Job Description

Hands on Exp in HPLC , GC and Physicochemical analysis (UV,IR,SOR,TLC Potentiometric titration including mentod development routine analysis & menthod validations along with good documentation practices

Hands on Exp in LC-Ms/GC-Ms including method develpoment, method validations and identification of unknown peaks along with good documentation practices.

Aware of regulatory guidelines, including USP/EP/IP Pharmacopeia's