U4-Technology Transfer-Executive 1

Sekhmet Pharmaventures Pvt Ltd.; Pashamylaram; On-site; INR 990,000 - 1,210,000; Full time

Job summary

Sekhmet Pharmaventures invites applications for an Executive position in the R&D department focused on technology transfer and documentation control. The role involves reviewing updated dossiers, gap assessments for manufacturing and raw materials, and coordinating batch reviews, stability protocols, and transfer activities between R&D and manufacturing.

The incumbent will work with cross-functional teams to ensure regulatory compliance, create BOM/BPR/MFC documents, and support CMOs with

Qualifications

• Post Graduate/M Pharma degrees are required
• Relevant pharmaceutics or R&D background is needed
• Experience with document review and tech transfer processes preferred

Responsibilities

• Review, extract and segregate updated dossier documents
• Review manufacturing gap assessments and BMR/BPR documentation
• Coordinate with cross-functional teams for transfer from R&D to plant and ensure regulatory compliance

Skills

Post Graduate

M Pharma

Education

M Pharma

Post Graduate

Job description

• Sekhmet Pharmaventures>Optimus Pharma (P) Ltd>OPPL-04>R&D>Tech Transfer>OPPL R&D Common>3800801903

Posted On 15 Oct 2026

End Date 29 Oct 2026

Required Experience NA

Basic Section

No. Of Openings 1

Grade L6D

Designation Executive 1

Campus/Non Campus Non Campus

Employment Type Full Time

Requisition Type New

Median 0 - 1100000

Comp off OT Applicability Comp off & Overtime

TAT 0

Confidential No

Closing Date 29 Oct 2026

Organisational

Company Sekhmet Pharmaventures

Entity Optimus Pharma (P) Ltd

Department R&D

Cost Centre 3800801903

Country India

Region South

Unit Unit-4

Skills

Skill

Post Graduate

M Pharma

Working Language

Job Description

Review & extraction & segregation of updated documents from dossier. Review of product manufacturing Gap assessment, Raw material gap assessment & packing material gap assessment. Review of engineering batch/ scale up batch BMR & sampling plan. Execution of Scale up batch, Exhibit batches at respective CMO’s. Review of batch reports, stability protocols & reports. Review of performing compatibility studies with respect to regulatory compliance. Coordinating with cross function teams, collection and sharing technical documents with FR&D, AR&D, Production, Quality assurance, Quality control and Regulatory affair departments. Preparation and review of batch records like BMR, BPR, stability protocols, stability reports, IC BMR. Scale up batches execution & batch records review
report. Responsible for RM, PM, SFG and FG code creation for new products. Analyze difference between equipment design and capacities and coordination with plant and other technical members in order smooth products transfer between R&D to plant. Review and finalization of draft BOM, MFC, MPC packing stability protocols sampling protocols in coordination with R&D production QA and documentation team. Involve in trouble shooting during transfer monitor execution of transfer revision of documents and process validation in order to enable smooth products transfer between R&D and plant. Support for manufacturing packing and engineering teams and trouble shooting for technical matters related to new projects new products introduction of smooth transfer of products from R&D to plant. Responsible for all QMS activities related to technology transfer products. CMO projects execution and supporting.