Job Responsibilities:
The candidate will be responsible for the dose formulation analysis for preclinical studies. He/She is expected to drive technical innovation in formulation method development and involved in validation, analysis of preclini...
Job Description (Posting).
1. Master's degree/ Ph.D. in pharmacology, Biotechnology, veterinary science, life sciences, or relevant science discipline.
2. Minimum 5 to 8 years of experience in preclinical toxicology and biocompatibility testing....
This role will lead a team of researchers to support projects related activities pertaining to
in vivo
oncology for different modalities (small molecules, biologicals, etc.) entailing new model development; screening and interpretation of resul...
...development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries around the world....
Key Responsibilities
Literature search safety data (preclinical and clinical) collection for identified issues seeking toxicology and/or clinical safety (skin tolerance) support.
Literature review for hazard assessment of ingredients intended ...
This role will lead a team of researchers to support projects related activities pertaining to in vivo oncology for different modalities (small molecules, biologicals, etc.) entailing new model development; screening and interpretation of results, ge...
Job Responsibilities:
The candidate will be responsible for the dose formulation analysis for preclinical studies. He/She is expected to drive technical innovation in formulation method development and involved in validation, analysis of preclinic...
...Join us as a Founder of our ‘new’ Sandoz!
Position Purpose:
Responsibility for the management, development and leadership of the group activities mainly for legacy products in accordance with the law, regulator...
1. Clinical and preclinical development of 505(b)(2) products: a. Literaturesearch focusing preclinical and clinical development programme
b. Understandingand defining the rationale of unmet need for identified product
c. Thoroughunderstandi...
...degradation product, extractable and leachable.
3. Genotoxicity hazard assessment for impurities using in-vitro and in-vivo data and in-silico (Q)SAR approaches (according to ICH M7 guideline).
4. Determination ...
