vacancies

Lead and guide the team for TPM Operations and functionality on GMP aspects and Abbott policies and procedures, though site visits and ensure an audit readiness of sites.

Lead teams to drive technical excellence and analytical problem-solving. Handle impurity profiling, degradation studies, structure elucidation, and method validation.

Gufic Biosciences Ltd is a leading pharmaceutical industry since 1970 and is one of the world’s largest Lyophilization injectables & wide range of API products, at Navsari

Prepare, compile, review, and submit product registration dossiers in CTD I eCTD format as per country-specific requirements and EAEU Unified Registration Procedure.

First / Second class M. Pharm. / M.S. Pharm.; Ph.D. Pharmaceutical Sciences. At least one publication in a SCI journal.

M.Pharm / M.Tech / MSc in Pharmaceutics, Pharmacology, Biotechnology, or related fields. First Division or equivalent, with strong motivation for research.

Ph.D. degree in Microbiology / Biochemistry / Biotechnology subject from a recognized University with 5 years R&D/ Teaching experience in the relevant subject after Ph.D.

First Class Postgraduate Degree in Life Sciences / Molecular Biology / Genetics / Biotechnology with 3 years of research experience OR PhD in a relevant subject

Masters Degree in Life Sciences / Biotechnology / Bioinformatics. Biomarkers for identifying GvHD post allogeneic hematopoietic stem cell transplantation.