Abbott is a global healthcare leader, committed to developing innovative products across pharmaceuticals, diagnostics, medical devices, and nutrition. With a presence in over 160 countries, Abbott strives to improve lives through high-quality healthcare solutions. The company offers its employees a collaborative and growth-oriented environment that values expertise and fosters continuous learning.
Core Responsibilities of the Scientist Role
As a Scientist at Abbott, you will play a key role in ensuring product continuity, operational excellence, and compliance with global regulatory standards. Your responsibilities will include:
- Analytical Method Development & Validation
- Develop, validate, and troubleshoot analytical methods for biosimilars, injectables, and vaccines.
- Provide technical expertise on high-performance liquid chromatography (HPLC), gas chromatography (GC), UV spectrophotometry, ELISA, electrophoresis, peptide mapping, bacterial endotoxins, and sterility testing.
- Product Transfer & Localization Support
- Collaborate with cross-functional teams during product technology transfers across regions, including APAC and MEAP regions.
- Support the localization of products considering cost efficiency and regulatory compliance.
- Issue Resolution & Risk Mitigation
- Troubleshoot operational issues to ensure uninterrupted product supply and prevent supply chain disruptions.
- Perform due diligence for new business deals and assess risks related to regulatory or technical gaps.
- Compliance & Laboratory Management
- Maintain compliance with global EQD standards in the analytical laboratory at the MS&T site in Goa.
- Manage laboratory instruments and equipment installation, qualification, and regular maintenance.
- Documentation & Reporting
- Prepare protocols, reports, and responses to regulatory deficiencies.
- Conduct analytical gap assessments and develop strategies to address identified gaps.
- Coordinate GeoEx projects and regulatory updates across regions.
- Leadership & Talent Development
- Manage the analytical laboratory at the MS&T Goa site and develop talent within the team to expand analytical expertise.
Educational Requirements:
- A Master’s degree in Pharmaceutical Science, Biotechnology, Microbiology, or a related discipline.
Work Experience & Expertise:
- Expertise in analytical method development and validation, especially for biosimilars, injectables, and vaccines.
- Hands-on experience with advanced analytical techniques like HPLC, GC, UPLC, ELISA, and PCR.
- Knowledge of pharmacopoeia standards, quality compliance, and regulatory requirements.
Key Skills:
- Strong analytical and problem-solving skills with a focus on statistical principles.
- Ability to collaborate across functions such as manufacturing, supply chain, regulatory affairs, and quality assurance.
- Agile mindset to adapt strategies based on emerging challenges.
- Excellent communication skills and proficiency in technology-driven tools.
Willingness to Travel:
- The role may require on-site support and travel to ensure smooth operations.
