MSAT Specialist

Company Description

CuraTeQ Biologics, a wholly owned subsidiary of Aurobindo Pharma Ltd., is an EU GMP-certified biopharmaceutical company headquartered in Hyderabad, India, with a mission to provide high-quality and cost-effective biosimilars to patients suffering from severe illnesses. The company has a robust development pipeline, which includes 14 biosimilars, several of which are in late-stage clinical trials or have received regulatory approvals from global authorities like EMA, MHRA, and EC. Notably, its approved products include Bevqolva® (Bevacizumab biosimilar), Dyrupeg® (Pegfilgrastim biosimilar), Zefylti® (Filgrastim biosimilar), and Dazublys® (Trastuzumab biosimilar). Committed to delivering better health outcomes, CuraTeQ is focused on oncology and immunology therapies, aspiring to become a global biosimilars leader by 2030.

Role Description

This is a full-time on-site role located in the Greater Hyderabad Area for an MSAT (Manufacturing Sciences and Technology) Specialist. The MSAT Specialist will oversee and provide technical support for manufacturing processes, lead process improvements, ensure compliance with quality and regulatory standards, and troubleshoot production issues. The role also includes analyzing data to optimize biotechnological manufacturing processes, preparing technical documentation, and collaborating with cross-functional teams to ensure efficient technology transfer and scalability of processes.

Qualifications

• Proficiency in biotechnology-related skills such as cell culture, downstream processing, and analytical techniques.
• Strong knowledge of GMP, process validation, and quality systems in a biopharmaceutical manufacturing environment.
• Experience with technology transfer, process development, and scale-up for biologics manufacturing.
• Excellent data analysis, technical writing, and documentation skills for creating reports and supporting regulatory submissions.
• Strong problem-solving, troubleshooting, and critical thinking abilities to address technical challenges in manufacturing operations.
• Effective communication and collaboration skills to work with cross-functional teams, including R&D, Quality Assurance, and Operations.
• Master's or Bachelor's degree in Biotechnology, Biochemistry, Chemical Engineering, or related field is required; advanced certifications or relevant experience in biopharmaceuticals is a plus.
• Experience with oncology or immunology therapeutic development is desirable.