Principle Scientist - Downstream R&D Curateq Biologics

12.0 - 16.0 years

16 - 25 Lacs

hyderabad

Work from Office

Role & responsibilities Position Summary: We at CuraTeQ Biologics are seeking a 12-16 year experienced Principle Scientist to join our Downstream Research & Development (R&D) team focused on monoclonal antibodies (mAb) and therapeutic proteins . The ideal candidate will have a strong background in bioprocess development, specifically in downstream purification and analytics of monoclonal antibodies and related complex protein molecules. This role will involve designing, optimizing, and scaling purification processes to support pipeline candidates and commercial biologics. Key Responsibilities: Lead early-stage process development and optimization of downstream purification processes, includi...

Posted -1 days ago

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Formulation Development Scientist Azurity Pharmaceuticals

3.0 - 7.0 years

0 Lacs

hyderabad, telangana

On-site

Azurity Pharmaceuticals is a specialty pharmaceutical company dedicated to providing innovative products for underserved patients. With a focus on unique, accessible, and high-quality medications, Azurity continuously expands its commercial product portfolio and late-stage pipeline through integrated capabilities and a vast partner network. The company's patient-centric products cover various markets including cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan, benefiting millions of patients globally. As an inclusive workplace and Equal Opportunity Employer, Azurity attributes its success to a talented and dedicated team committed to improving patients" l...

Posted 1 week ago

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Manager GMP (Good Manufacturing Practices) QA (Quality Assurance) Ocugen

8 - 10 years

12 - 15 Lacs

Hyderabad

Work from Office

Job title manager GMP (Good Manufacturing Practices) QA (Quality Assurance) Reports to Head of Quality Assurance (GMP and GCP) Job purpose Our Quality team is growing, and we are currently seeking a Manager of GMP QA Operations to play a pivotal role in ensuring the quality and compliance of our clinical and commercial manufacturing processes. Reporting to the Head of QA, the Manager will oversee a team responsible for manufacturing, batch record release, investigations, deviations, CAPAs (Corrective and Preventive Actions), change controls, analytical methods, stability programs, and auditing within our GMP operations. Duties and responsibilities QA managers define and implement quality sta...

Posted 4 months ago

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