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Opportunity for Scientist at Biocon Pharma Limited

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Opportunity for Scientist at Biocon Pharma Limited

Biocon is global biopharmaceutical company changing patients' lives in over 120 countries by finding new and affordable ways to treat diabetes, cancer and autoimmune diseases. Biocon is a research-driven, global healthcare company with a strong matrix of capabilities along the biopharmaceutical value chain.

Post : Scientist (10565)

Job Description
Role Summary
Looking for GF Analytical - OSD Expertise. - For Scientist / Senior Scientist level

1. Experienced in analytical development & characterization, evaluation interpretation through below techniques: a. Versatile chromatographic techniques (SEC, IEC etc)
2. Validation of analytical methods by various instrumental techniques to support the formulation product developments for regulatory dossier submissions.
3. Peptide mapping, finger printing & characterization e.g. LC MS/MS, HRMS etc.
4. NMR and other spectroscopic techniques
5. Experienced in analytical characterization of peptides, complex molecules and non-conventional dosage forms.
6. Experienced & skilled in analytical development for various dosage forms of peptides & complex generics moieties.


Key Responsibilities
-  Analytical characterization of peptides, complex molecules and non-conventional dosage forms.
- Skilled in analytical development for various dosage forms of peptides & complex generics moieties.
- Involve in implementing QbD principles and tools to analytical methods considering total product life cycle.
- Proficient in GMP documentations and to assist in preparation of protocols & reports for analytical activities, and review the analytical data.
- Understanding of USFDA, EMA, MHRA, and ICH guidelines, and the regulatory requirements of various International Regulatory Agencies.
- To handle procurement, installation & qualification of analytical equipment to set up and maintain a GLP compliant analytical testing lab.
- Transfer of analytical technology and methods to the manufacturing site for regular QC testing.
- Knowledge to Design and conduct in-vitro drug release testing of solid and semi-solid formulations with various dissolution techniques,
- Knowledge to develop discriminatory and bio-relevant dissolution methods.

Additional Information
Experience : 2 - 6 years
Qualification : M.Sc
Location : India
Industry Type : Pharma / Healthcare/ Clinical research
Functional Area : Analytical R&D
End Date : 30th April, 2023


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