Sekhmet Pharma walk ins for AR&D / RA / RA(Licensing) / IPM / IT Departments on 11th July 2026 - Pharmawisdom.co.in

Sekhmet Pharmaventures, a part of the Optimus Group, is conducting a Walk-in Interview for experienced professionals across Analytical Research & Development (AR&D), Regulatory Affairs (RA), Regulatory Affairs – Licensing, Intellectual Property Management (IPM), and Technology Transfer (TT) departments. Candidates with relevant pharmaceutical experience are invited to attend the recruitment drive at the Optimus R&D Center, Hyderabad.

Particulars Details
Company Name Sekhmet Pharmaventures (Optimus Group)
Departments AR&D, RA, RA (Licensing), IPM & Technology Transfer
Job Type Full-Time
Industry Pharmaceutical / API Research & Development
Experience Required 2–5 Years
Interview Date 11 July 2026
Interview Time 8:30 AM – 3:00 PM
Interview Mode Walk-in Interview
Job Location Hyderabad, Telangana
Department Job Title Experience Qualification
Analytical R&D (AR&D) Executive / Senior Executive 2–5 Years M.Sc. (Analytical Chemistry)
Regulatory Affairs (RA) Executive 4–5 Years M.Sc. (Chemistry)
Regulatory Affairs (Licensing) Executive 2–4 Years M.Pharm / M.Sc.
Intellectual Property Management (IPM) Senior Executive 2–5 Years M.Sc. (Organic Chemistry)
Technology Transfer (TT) Senior Executive 4–5 Years B.Tech (Chemical Engineering)

Candidates should possess any one of the following qualifications based on the role:

  • M.Sc. (Analytical Chemistry)
  • M.Sc. (Chemistry)
  • M.Sc. (Organic Chemistry)
  • M.Pharm
  • B.Tech (Chemical Engineering)

🧪 Analytical R&D (AR&D)

Executive / Senior Executive

  • Perform analytical method development and validation.
  • Conduct analytical testing using laboratory instruments.
  • Support stability studies and impurity analysis.
  • Prepare analytical documentation in compliance with cGMP and GLP.
  • Ensure data integrity and regulatory compliance.

📑 Regulatory Affairs (RA)

Executive

  • Prepare and review regulatory dossiers.
  • Support product registration activities.
  • Ensure compliance with national and international regulatory guidelines.
  • Coordinate with cross-functional teams for submission activities.
  • Maintain regulatory documentation.

🌍 Regulatory Affairs (Licensing)

Executive

  • Manage licensing documentation and agreements.
  • Coordinate licensing activities with internal and external stakeholders.
  • Prepare regulatory documents for product registrations.
  • Ensure timely submission of licensing requirements.
  • Maintain regulatory compliance records.

💡 Intellectual Property Management (IPM)

Senior Executive

  • Support patent search and intellectual property activities.
  • Analyze patent literature and scientific publications.
  • Assist in patent documentation and filing activities.
  • Coordinate with R&D teams on IP-related matters.
  • Maintain IP documentation and compliance.

🔄 Technology Transfer (TT)

Senior Executive

  • Coordinate technology transfer activities from R&D to manufacturing.
  • Prepare technology transfer documents and protocols.
  • Support process scale-up and validation.
  • Coordinate with production and quality teams.
  • Ensure smooth transfer of manufacturing processes.

Analytical R&D

  • Analytical Method Development
  • Method Validation
  • Laboratory Documentation
  • Stability Studies
  • cGMP & GLP Compliance
  • Data Integrity

Regulatory Affairs

  • Regulatory Documentation
  • Product Registration
  • Dossier Preparation
  • Regulatory Compliance
  • Submission Management

Regulatory Affairs (Licensing)

  • Licensing Documentation
  • Regulatory Affairs
  • Compliance Management
  • Documentation Control

Intellectual Property Management

  • Patent Search
  • Patent Documentation
  • Scientific Literature Review
  • Intellectual Property Management

Technology Transfer

  • Technology Transfer
  • Process Scale-up
  • Process Validation
  • Manufacturing Coordination
  • Technical Documentation
Event Details
Interview Date 11 July 2026
Reporting Time 8:30 AM
Interview Timing 8:30 AM – 3:00 PM

Optimus R&D Center
Optimus Drugs (P) Limited (R&D Centre)
Plot No. 64
Survey No. 144, Part, EPIP
Pashamylaram Village
Near Isnapur
Sangareddy District
Hyderabad, Telangana

Candidates should bring:

  • Updated Resume/CV
  • Educational Certificates (Original & Photocopies)
  • Experience Certificates
  • Last 3 Months Payslips
  • Latest Salary Breakup
  • Government Photo ID Proof (Aadhaar/PAN/Passport/Driving Licence)
  • Recent Passport-size Photographs
  • Professionals with 2–5 years of pharmaceutical industry experience in AR&D, Regulatory Affairs, Licensing, Intellectual Property Management, or Technology Transfer.
  • Candidates possessing the required educational qualifications.
  • Professionals with strong technical knowledge, documentation skills, and regulatory compliance experience.
  • Candidates willing to work at the Hyderabad R&D Centre.
  • Opportunity to work with the Optimus Group, a reputed pharmaceutical organization.
  • Exposure to advanced research and development projects.
  • Career growth in Analytical R&D, Regulatory Affairs, Intellectual Property, and Technology Transfer.
  • Professional work environment with continuous learning and development opportunities.
  • Collaborative culture focused on innovation and quality.

📢 Important Note

Candidates attending the walk-in interview on 11 July 2026 are requested to carry their updated resume, educational documents, last three months’ payslips, latest salary breakup, and valid photo ID proof. Reporting early will help ensure a smooth interview and document verification process.

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