Torrent Pharma Hiring for Biopharmaceutics (Clinical Research) – Executive
Torrent Pharma is inviting applications for the position of Executive – Biopharmaceutics (Clinical Research) at their state-of-the-art R&D center in Gandhinagar, Gujarat. This is an excellent opportunity for skilled professionals with expertise in pharmacology and clinical research to contribute to groundbreaking projects in biopharmaceutics.
About Torrent Pharma
Torrent Pharma is a global pharmaceutical leader known for its focus on quality, innovation, and patient-centric solutions. Headquartered in India, the company specializes in producing high-quality generics, biosimilars, and research-driven formulations. Its R&D center in Gandhinagar, Gujarat, is a hub of innovation, making it an ideal place for career growth and development in the pharmaceutical sector.
Job Overview
- Position: Executive – Biopharmaceutics (Clinical Research)
- Location: Torrent Pharma R&D Centre, Gandhinagar, Gujarat
- Department: Biopharmaceutics (Clinical Research)
- Qualification: M.Pharm (Pharmacology)
- Experience Required: 2 to 5 years
Torrent Pharma, a leader in pharmaceutical innovation, offers an excellent opportunity to contribute to cutting-edge research and development in biopharmaceutics and clinical studies.
Key Responsibilities
- Feasibility Assessments: Conduct evaluations for new product feasibility and assess innovative biopharmaceutical projects.
- Literature Review & Study Design: Perform detailed literature reviews and design Bioequivalence (BE) studies.
- Study Monitoring: Monitor the execution of BE studies to ensure compliance with regulatory and scientific standards.
- Regulatory Documentation: Prepare documents for regulatory submissions such as BENOC and import license applications.
- Dossier Preparation: Develop clinical and non-clinical overviews, along with summary tables for dossier submissions.
- Document Reviews: Review BE study protocols, reports, and Informed Consent Forms (ICFs).
- Medical Writing: Draft or review medical and scientific documents, including safety updates and adverse event reports.
- Regulatory Coordination: Ensure timely reporting of serious adverse events and maintain regulatory compliance.
Skills and Requirements
- Educational Qualification: M.Pharm in Pharmacology.
- Experience: 2-5 years in biopharmaceutics, clinical research, or related roles.
- Key Skills:
- Expertise in BA/BE study design and monitoring.
- Proficiency in regulatory documentation and dossier preparation.
- Strong analytical and medical writing skills.
- Knowledge of adverse event reporting and safety protocols.
How to Apply
Interested candidates can share their updated resumes with the subject line: “Application for Executive – Biopharmaceutics” to the following email addresses:
- Megha Maheshwari: meghamaheshwari@torrentpharma.com
- Vilsha Shah: vilshashah@torrentpharma.com
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