Scientist - Toxicology Aurigene Pharmaceutical Services Limited

3.0 - 7.0 years

0 Lacs

hyderabad, telangana

On-site

As a Scientist in General Toxicology, your role will involve the following: - Serving as a Study Director for general toxicology studies including acute, repeated dose toxicity studies, and PK studies. - Acting as a Study Personnel for general toxicology studies led by other Study Directors. - Responsible for preparing study plans, study plan amendments, deviations, study reports, SOPs, and conducting their reviews. - Ensuring the maintenance of in vivo laboratory and providing assistance in departmental activities as needed. - Conducting validation of new studies to enhance the capabilities of the team. - Compiling, verifying, and performing statistical analysis of study data. - Managing th...

Posted 2 days ago

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Analyst Brooks steriscience Ltd

2.0 - 6.0 years

0 Lacs

vadodara, gujarat

On-site

You will be responsible for conducting GLP activities in the laboratory to ensure compliance with regulatory standards. Your key responsibilities will include: - Performing GLP studies according to protocols and standard operating procedures - Collecting, recording, and analyzing data accurately - Maintaining laboratory equipment and facilities to meet GLP requirements - Participating in GLP audits and inspections Qualifications required for this role: - Bachelor's or Master's degree in a relevant scientific discipline - Prior experience with GLP studies in a laboratory setting - Strong attention to detail and organizational skills - Excellent communication and teamwork abilities,

Posted 4 weeks ago

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Scientist - Toxicology Aurigene Pharmaceutical Services Limited

3.0 - 7.0 years

0 Lacs

hyderabad, telangana

On-site

You will be responsible for functioning as a Study Director for general toxicology studies, including acute, repeated dose toxicity studies, and PK studies. Additionally, you will function as a Study Personnel for general toxicology studies led by other Study Directors. Your duties will involve the preparation of study plans, study plan amendments, deviations, study reports, SOPs, and their review. Furthermore, you will be tasked with maintaining the in vivo laboratory and providing assistance in departmental activities as required. In order to enhance the capabilities of the team, you will be required to perform validation of new studies. Your role will also include the compilation, verific...

Posted 3 months ago

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