The Life Sciences sector in Nashik is renowned for its commitment to delivering cutting-edge solutions in biotechnology and pharmaceutical manufacturing. This company emphasizes a culture of innovation, GMP compliance, and global standards, providing employees with an environment that fosters professional growth. With state-of-the-art facilities and advanced technology, the company is dedicated to achieving excellence in product quality and operational efficiency.
Responsibilities in the Role of Young Professional
The position of Young Professional offers an exciting blend of technical and supervisory responsibilities:
1. Manufacturing and Project Execution
- Ensuring manufacturing processes adhere to SOPs.
- Operating and troubleshooting process systems while removing bottlenecks in production.
- Facilitating upstream and downstream processing, including bioreactor operations and skid system management.
- Utilizing DCS control systems and supporting scale-up or scale-down processes.
- Collaborating with cross-functional teams to meet production goals.
2. Review and Monitoring
- Preparing and maintaining cleaning schedules, solutions, and fumigation activities.
- Managing GMP documentation such as BMRs, BPRs, and logbooks.
- Ensuring compliance with cGMP standards and preparing documents for regulatory audits.
- Supervising and training team members to meet performance and safety expectations.
3. Validation and Audit Readiness
- Supporting the calibration, preventive maintenance, and qualification of equipment.
- Preparing for FDA, WHO, and international GMP audits.
- Developing validation protocols and ensuring their successful execution.
Qualifications for the Role
- A graduate or postgraduate degree in Science or a B.E. in Biotechnology Engineering is required.
- Candidates with 0-1 years of experience are encouraged to apply, making this an ideal role for recent graduates.
Key Skills and Competencies
- Technical Proficiency: Hands-on experience with bioreactors, chromatography, TFF, and CIP systems.
- Documentation: Strong knowledge of GMP documentation and practices.
- Leadership: Ability to supervise and train team members effectively.
- Audit Preparation: Familiarity with regulatory guidelines, including FDA and WHO standards.
- Safety Awareness: Commitment to occupational health, safety, and environmental management.
