Handling Granulation and Compression activities. Operation of granulator, blender and compression machines. Compliance with CMP, SOP, and safety norms.
Experienced Shift In Charge to Manage daily manufacturing Operations, ensuring strict cGMP, Safety and regulatory Compliance. Key duties include production planning & ensuring execution as per plan, preparing batch records and qualification documents.
BPharma in Biotechnology / Food and Nutritional Sciences / Technology / Instrumentation / Agricultural Biotechnology OR equivalent qualification with 02 years of relevant experience.
Bachelors Degree in Pharmacy from an Institution recognized by the Central or State Govt. Should be registered as a Pharmacist under the Pharmacy Act, 1948.
PhD in any branch of Life Sciences / Agricultural Biotechnology / Food and Nutrition Sciences / Food Technology or equivalent with 05 years experience or ME/M.Tech in Agri- Biotechnology/ Biotechnology/ Chemical Technology / Food Technology / Food Sciences
MSc Clinical Research, and age less than 30 years. Candidates with experience of working as Clinical Research Coordinator in a Clinical Trial will be given preference
Ph.D. with First Class or equivalent in the preceding degree and a good academic record throughout. Candidates who have submitted their Ph.D. thesis can also apply by providing proof of thesis submission. Candidates should preferably be less than 32 years of age at the time of applying.
The Alexander von Humboldt Foundation aims to achieve a good balance between genders and a high level of diversity among its fellows in all areas. We therefore expressly invite female scientists and members of underrepresented groups to apply. We welcome all applications, regardless of ethnic, cultural or social background, gender identity, age, religion, worldview, disability or sexual orientation.
Sri Krishna Pharmaceuticals Ltd, established in 1974, started life as a pioneer in the bulk manufacture of acetaminophen Paracetamol for the domestic Indian market.
High level of expertise in the lifecycle management of radiopharmaceutical products, including CMC authoring, safety labelling experience, artworks annotations
Ph.D or equivalent degree or having 3 years of research, teaching and design and development experience after MVSc/ M.Pharma/ ME/ M.Tech with at least one research paper in Science Citation Indexed journal.