Research Scientist RIBOSOME RESEARCH CENTRE PVT. LTD.

1.0 - 5.0 years

0 Lacs

surat, gujarat

On-site

You should have a qualification of M. Pharm (Pharmacology) or M.Sc. in Zoology/Toxicology with 1 to 3 years of experience, preferably in a Contract Research Organization (CRO). Your responsibilities will include handling animals like rat, mice, guinea pig, and rabbit, as well as knowledge of various routes of administration such as oral, intravenous, subcutaneous, and dermal. You will also be required to collect biological samples like blood, have a basic understanding of animal testing, and possess knowledge of OECD guidelines. Basic computer knowledge is also essential for this role. In terms of benefits, you can enjoy a large campus with leave facilities including Casual Leave, Privilege Leave, and Sick Leave. Additionally, there are perks like school/college fees deduction for employees" staff, yearly Annual Health Check-Up Report, gym facility, hostel and canteen facility, employee engagement activities, tours, training, and more. This is a full-time, permanent position. Other benefits include food provided, leave encashment, paid sick time, and paid time off. The key skills required for this role include basic computer knowledge, knowledge of OECD guidelines, biological sample collection, in vivo testing, understanding of animal testing, GLP, pharmacology, preclinical research, and animal handling among others.,

Posted 2 days ago

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Invivo Mice Scientist AVE-Promagne Business Solutions

2.0 - 7.0 years

10 - 11 Lacs

Hyderabad

Work from Office

You get to collaborate on: Work closely with discovery specialists, disease area scientists and in vivo team members. Handling of laboratory animals like rat, mice, Guniea Pig and Rabbits. Dose administration to experimental animals by different routes and small animals surgery (like cannulations, CSF fluid collection) and handling, followed by compound dose preparation, administration to experimental animals. Contributing to the ongoing drug discovery programs by conducting in vivo DMPK studies for NCEs with a good knowledge of in vivo animal models. Data generation, analysis, compilation, report preparation. Regular uploading of the data. Conduct statistically supported data (analysis using win online) and deliver results in a timely manner to enable informed decision-making Understanding systems, processes, and compliance. Prepare, review, and deliver scientific presentations for internal/external use. Participate in cross-functional team activities, add value to research projects through creative ideas. Learn from top-notch drug discovery scientists across the world and opportunity to get trained in people skills. PK-PD studies in rat and mice of NCE.

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Study Director -In-vivo Toxicology Syngene

3.0 - 8.0 years

4 - 8 Lacs

Bengaluru

Work from Office

Core Purpose of the Role: As a Study Director - Toxicology: Responsible for ensuring that GLP toxicology studies; acute, repeat dose and reproduction are carried out to the required scientific and regulatory standards as per Global regulatory guidelines [ICH/OECD]. Function as single point of study control, overall responsibility for the scientific, technical and regulatory conduct of studies, scientific interpretation, documentation and reporting of results. Role Accountabilities: Study Director for in vivo toxicology studies Coordination with local cross-functional teams like veterinary science, biopharmaceutics, bioanalysis, pharmacokinetics or in vitro biology before, during and after execution of toxicology studies Conduct of in-life phases of toxicology studies in rats, mice and rabbits Dose administration in rats, mice and rabbits with various routes of administration Use of on-line data capture system- Pristima Blood sample collection for toxicokinetic Assistance during necropsy activities such as organ weighing, data entry in PROVANTIS software Assistance in conducting rabbit electrophysiology studies Coordination with veterinary science team IAEC meetings- preparation and maintenance of FORM-B and FORM-D Blood collection in rats and mice via different routes for clinical pathology analyses Preparation and following of in-house SOPs Co-ordination for preventive maintenance and calibration of instruments. Archival of materials from toxicology studies. Any other duties given from time to time by the line manager

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Senior Executive / Assistant Manager - IVIVC AET Laboratories

5.0 - 10.0 years

9 - 17 Lacs

Hyderabad

Work from Office

Job Responsibilities : Develop and validate IVIVC and PBPK models to predict in vivo drug performance from in vitro data. Conduct in vitro experiments such as solubility, dissolution, and permeability studies using biorelevant media. Collaborate with formulation, analytical, and clinical teams to optimize drug product development. Analyze bioequivalence (BE) study data and support regulatory submissions with modeling insights. Prepare and review technical reports, protocols, and regulatory documentation . Preferred candidate profile & Qualifications: Should be well versed with IVIVC concepts,preferably 5-10 years of experience. Should have excellent knowledge on product development and clinical studies. Should have hands on experience on operating various simulation tools necessary for IVIVC. Excellent communication skills are must. Strong knowledge of oral solid dosage forms (OSDs) and excipient functionality. Experience with regulatory guidelines (e.g., USFDA, EMA) related to IVIVC and BE studies. M.Pharm or Ph.D. in Pharmaceutics, Biopharmaceutics, or Pharmaceutical Sciences.

Posted 1 month ago

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