Description

Job description:

• • • Planning/performing and reporting of acute toxicology studies
    • Assist in preparation of SOP’s, Protocols and Reports
    • Participate in GLP / AAALAC related activities
    • Literature search  
    • Maintenance of animal house and relevant documents as per GLP and AAALAC norms.
    • To Assist and work along with SD and TC in Planning, initiation and conduct studies.
    • Test item administration, dose formulation preparation and blood collection.
    • Assistance in data collection, compilation and verification.
    • Participate in GLP inspections and ensure relevant regulatory compliance guidelines.
    • Support in interpretation and reporting of study data.
    • Assist in report preparation and coordination of activities.
    • Assist in archiving of all study related materials.

Skills Required:

• • • Understanding of the agrochemical and pharmaceutical R&D process

Behavioral Competencies:

• • • Good in oral / written communication skills.

If you're interested in applying or learning more, send your updated resume to hr.advinus@advinus.eurofinsasia.com with the subject line "Research Scientist/Senior Research Scientist - Acute – Toxicology  - Bangalore".

Qualifications

Qualification

M.Sc. in Zoology/Biosciences

Additional Info

Specialization

Toxicology

Department

Acute – Toxicology  

Experience (years)

2 to 8  only

Company Description

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies.

With over 30 years of GLP compliance and certification, Eurofins Advinus serves diverse industries such as Biotech, Pharmaceutical, Biological, Agrochemical, Nutraceutical and Cosmetic. Eurofins Advinus is the only contract research organization (CRO) in India to have developed data in support of 90+ end-to-end IND enabling packages to be submitted to global regulators such as USFDA, EMA, MHRA, Health Canada and others.