Auxilife is currently hiring for the role of Scientific Officer / Senior Scientific Officer โ Bioefficacy in Pune (Wakad). This is an excellent opportunity for candidates with 0โ3 years of experience who want to build a career in bioefficacy trials, regulatory compliance, and scientific research within the life sciences domain.
With increasing global focus on GLP (Good Laboratory Practices) and GEP (Good Experimental Practices), this role offers hands-on exposure to protocol development, CRO collaboration, and regulatory dossier preparationโmaking it highly relevant for candidates targeting careers in clinical research, regulatory affairs, and scientific consulting.
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๐ Job Overview
- Company: Auxilife
- Role: Scientific Officer / Senior Scientific Officer โ Bioefficacy
- Experience: 0โ3 Years
- Location: Pune (Wakad), India
- Salary: โน2.4 โ โน3.6 LPA (approx.)
- Employment Type: Full-Time, Permanent
๐งช Key Responsibilities
As a Scientific Officer Bioefficacy, you will:
- Design and oversee bioefficacy trials as per global regulatory guidelines
- Develop study protocols in collaboration with CROs
- Review scientific data, trial reports, and ensure accuracy
- Prepare regulatory dossiers for submissions
- Ensure compliance with GLP/GEP standards
- Coordinate with cross-functional teams (R&D, regulatory, operations)
- Track evolving regulatory requirements and scientific standards
- Mentor junior scientists and support project execution
- Manage multiple projects within defined timelines
๐ Qualifications & Skills
Educational Requirements:
- Postgraduate degree (M.Pharm, MSc, PharmD, Life Sciences or related field)
Required Skills:
- Scientific writing & technical communication
- Data analysis and interpretation
- Knowledge of bioefficacy studies and trial design
- Project management & stakeholder coordination
- Understanding of GLP/GEP compliance
- Problem-solving and strategic thinking
๐ผ Benefits of This Role
- Early-career opportunity in bioefficacy and regulatory science
- Exposure to global research standards and compliance frameworks
- Hands-on experience in protocol design and dossier preparation
- Career pathway into clinical research, CROs, and regulatory affairs
- Opportunity to work in a collaborative scientific environment
๐ฅ How to Apply
