Sekhmet Pharmaventures has announced a Walk-In Interview Drive for experienced professionals in Research & Development, Regulatory Affairs, Licensing, IPM, and Technology Transfer departments. The recruitment drive will be conducted on 11th July 2026 at the Optimus R&D Center, Hyderabad.

Candidates with relevant pharmaceutical industry experience and the required educational qualifications are invited to attend the interview.

Job Overview

Particular Details

Company

Sekhmet Pharmaventures

Interview Type

Walk-In Interview

Walk-In Date

11 July 2026

Interview Time

8:30 AM – 3:00 PM

Job Location

Hyderabad, Telangana

Venue

Optimus R&D Center, Optimus Drugs (P) Ltd. (R&D Centre), Plot No. 64, Survey No. 144/Part, EPIP, Pashamylaram (V), Near Isnapur, Sangareddy, Hyderabad

Available Positions

1. Analytical Research & Development (AR&D)

Position: Executive / Senior Executive

Experience: 2–5 Years

Qualification: M.Sc. in Analytical Chemistry

2. Regulatory Affairs (RA)

Position: Executive

Experience: 4–5 Years

Qualification: M.Sc. Chemistry

3. Regulatory Affairs (Licensing)

Position: Executive

Experience: 2–4 Years

Qualification: M.Pharm / M.Sc.

4. IPM

Position: Senior Executive

Experience: 2–5 Years

Qualification: M.Sc. Organic Chemistry

5. Technology Transfer (TT)

Position: Senior Executive

Experience: 4–5 Years

Qualification: B.Tech in Chemical Engineering

Documents Required

Candidates should carry:

Updated Resume/CV

Educational Certificates

Government Photo ID

Passport-size Photographs

Last 3 Months’ Payslips

Latest Salary Breakup (CTC Details)

Experience Certificates (if applicable)

Skills Preferred

Knowledge of cGMP, GLP and ICH Guidelines

Strong documentation practices

Analytical and problem-solving skills

Good communication and teamwork

Experience in pharmaceutical research and regulatory compliance

Ability to work in a regulated environment

Why Join Sekhmet Pharmaventures?

Career opportunities in a leading pharmaceutical organization

Exposure to advanced R&D and regulatory projects

Professional growth with experienced teams

Competitive salary and employee benefits

Modern research and development infrastructure

Selection Process

Walk-In Registration

Document Verification

Technical Interview

HR Discussion

Final Selection

Important Note

Candidates are requested to bring their last three months’ salary slips along with the latest salary breakup during the interview.

Technical FAQs

1. What analytical instruments should an AR&D candidate be familiar with?

Candidates should have hands-on knowledge of HPLC, GC, UV-Visible Spectrophotometer, FTIR, Dissolution Apparatus, and related analytical techniques used for method development and validation.

2. What is the primary responsibility of a Regulatory Affairs (RA) Executive?

An RA Executive prepares and reviews regulatory dossiers, ensures compliance with ICH, FDA, EMA, and CDSCO guidelines, and supports product registrations and lifecycle management.

3. What is Technology Transfer (TT) in the pharmaceutical industry?

Technology Transfer involves transferring a manufacturing process from R&D or pilot scale to commercial production while maintaining product quality, consistency, and regulatory compliance.

4. What are the key responsibilities of an IPM Senior Executive?

IPM professionals coordinate project timelines, monitor product development activities, manage cross-functional communication, prepare reports, and ensure timely project execution.

5. Which GMP guidelines are important for experienced pharmaceutical professionals?

Candidates should have a good understanding of cGMP, Good Documentation Practices (GDP), Data Integrity (ALCOA+), Quality Risk Management (ICH Q9), and relevant ICH guidelines.