Pharma Jobs

Candidates having Ph.D Degree in Bioinformatics, Biotechnology, Botany, Life Sciences, Plant Molecular Biology or equivalent and fulfilling the guidelines. Candidates with exhaustive work experience in the laboratory with plant molecular biology, biochemistry and, or bioinformatics will be preferred.

Basic knowledge of molecular and immunological techniques and animal handling. BSL-3 handling and experimentation is desirable. Exploration of Immunopathogenesis of extra-intestinal organ involvement in patients with Celiac disease. Masters degree in any branch of Life Sciences from a recognized University.

Supervise and lead the team of analytical development, Analytical method validation, technology transfer, forced degradation study, preformulation study, dissolution studies, Extractable and Leachable and technical query handling. Candidates must have exposure of Pharma regulatory approved organisations USFDA, MHRA, Eu and other Major regulatory bodies

Exposure to OSD Manufacturing operations like Granulation, Compression, Pellet coating, Capsule filling, Primary Packing and Secondary Packing. Expertise in e-BPR and e-log will be added advantage. Experience in analysis of Solid Oral - FP, In-process or Stability samples. Experience of HPLC, UV spectrophotometer and Dissolution Tester operation. Experience of Analytical Method Validation/Transfer Solid Oral. Experience of GC, ICPMS and/or LCMS operation.

Lead and mentor a team of research scientists and chemists. Oversee projects, ensuring timely, budget-friendly, and high-quality delivery. Provide expertise in solving complex synthetic challenges and optimising reactions

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 (Gujarat). International accreditation of WHO, GMP, EU, Canada, Russia, Anvisa, etc.

Analytical Method Development, Validation, Transfer activities of test like Assay, RS, Dissolution and Solvent. Calibration of the Analytical instruments like HPLC, GCHS, IR, UV & Disso as per the master calibration schedule. Carry out routine analysis & Ensure documents pertaining to day to day analysis.

Reviews all Annual Product Quality Review APQR reports received from manufacturing partners and prepares APQR reports other than those received from the manufacturers within the prescribed time frame.

Collaborate with outsource parties to full fill laboratory requirement in timely manner. Previous experience in analytical method validation would be an added advantage.