Post: Research Associate - Pharmaceutical Development
Desired Profile
- M.Pharm. in Pharmaceutics with 2-4 yrs experience in NCE pre-formulation and formulation development, more preferably in protein/peptide NCE formulation development.
- Should be well versed with NCE pre-formulation and formulation especially in stages of pre-clinical development and IND-enabling studies.
- Should be well versed with the guidance documents pertaining to Quality and Pharmaceutical Development
- M.Pharm. in Pharmaceutics with 2-4 yrs experience in NCE pre-formulation and formulation development, more preferably in protein/peptide NCE formulation development.
- Should be well versed with NCE pre-formulation and formulation especially in stages of pre-clinical development and IND-enabling studies.
- Should be well versed with the guidance documents pertaining to Quality and Pharmaceutical Development
Job Description, Key Skills and Competencies:
- Should prepare and support test item formulations for regulatory (GLP) toxicity studies and non-regulatory non-clinical pharmacokinetic, efficacy and toxicity studies.
- Should be able to undertake formulation feasibility and development with minimal supervision.
- Should have thorough understanding of physico-chemical properties and their influence on bio-availability of the NCEs.
- Should be able to handle HPLC systems of Waters, Agilent and Schimadzu with minimal supervision
- Should be able to prepare protocols, guidelines, SOPs for lab equipments/instruments and processes and should be proficient in GLP documentation.
- Should be proactive in maintenance of processes and systems of the functional area.
- Should have a basic understanding of systems and process pertaining to safety, health and environment.
- Should prepare and support test item formulations for regulatory (GLP) toxicity studies and non-regulatory non-clinical pharmacokinetic, efficacy and toxicity studies.
- Should be able to undertake formulation feasibility and development with minimal supervision.
- Should have thorough understanding of physico-chemical properties and their influence on bio-availability of the NCEs.
- Should be able to handle HPLC systems of Waters, Agilent and Schimadzu with minimal supervision
- Should be able to prepare protocols, guidelines, SOPs for lab equipments/instruments and processes and should be proficient in GLP documentation.
- Should be proactive in maintenance of processes and systems of the functional area.
- Should have a basic understanding of systems and process pertaining to safety, health and environment.
Additional Information:
Experience: 2-4 Years
Location: Hyderabad
Functional Area: R&D
Industry Type: Pharma/ Biotech/Clinical Research
Employment Type: Full Time
Job Type: Regular
End Date: 30th June, 2014
Experience: 2-4 Years
Location: Hyderabad
Functional Area: R&D
Industry Type: Pharma/ Biotech/Clinical Research
Employment Type: Full Time
Job Type: Regular
End Date: 30th June, 2014
Please send your profile to careers@aurigene.com
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