Research AssociateJobs Opening in Cadila Pharmaceuticals Ltd at Dholka
Research Associate
Cadila Pharmaceuticals Ltd
Posted: 17 Dec 25
Job Description
Core responsibility related to GLP:
Study Personnel (Toxicology & Efficacy studies)
- Record raw data accurately and directly and in compliance with Principles of GLP during conduct of activity, verify the data collected, prepare reports and archive these records.
- Request for test and reference item and its receipt, safe handling and disposal as per in-house SOPs.
- Preparation and labelling of reagents, solutions chemicals and testing samples in the laboratory areas
- Wearing appropriate protective clothing and follow all safety precautions
- Operation, calibration, cleaning, labelling and maintenance of instruments used for routine activity and maintain these records
- Maintain cleanliness of the area/section.
- Procurements of materials for conduct of experimental activity in laboratory.
- Request for controlled documents and maintain accountability as per in-house SOPs
- To co-operate during internal, RQA & sponsor audits of study plans, studies, data, reports and facility etc.
- Preparation of SOPs relevant to activities performed in laboratory area, conduct the training on SOPs
- Follow the instructions given in SOPs and study plan.
- Document the deviation from study plan & SOP and communicate directly with SD.
- Maintenance of internal records as per in-house SOPs and GLP
- Update and maintain training records
- Ensure the availability of various monitoring certificates such as feed, water, bedding material, health etc.
- Literature search for the studies
- Perform the study activities listed below but not limited to:
- Feeding, watering, cage changing and other husbandry practices
- Weighing of animals
- Randomization of study animals
- Dose preparation & dosing of animals
- Observe the study animals for clinical signs, neurobehavioral and functional observation battery and mortality
- Measure and record the body temperature
- Perform Draize observations and other dermal observation
- Collection of sample(s) / Specimen(s).
- Receipt, storage and handling of chemicals, reagents and solutions
- Participate in mutagenicity / genotoxicity studies
- Participate in standardization of new toxicity study
- Perform room activities like recording of room temperature, humidity, lux etc.
- Fogging of rooms
- Data entry from raw data to computer application and further analysis including statistical programs
- Preparation of raw data file, reports and specimen for archiving.
Allied responsibility:
- Following GPCB guidelines for waste management system and maintenance of its records
- To ensure pest control at test facility
- Performing assigned duties on weekly off and holidays based on requirements
- Create purchase request for material and follow up
Any additional responsibility / activity as and when assigned by management which would not arise any conflict of interest.
Job Particulars
Role research jrf srf
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2809162
Job Category Research
Locality Address
State
Country India
About Company
Cadila Pharmaceuticals Ltd
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