Intas Released Job Openings On 12/12/2022.Intas Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon. With expertise in a range of formulations, from tablets to injectables to newer drug delivery systems, Intas is currently ranked 17th among the Indian Pharma majors..Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Intas Recruitment 2021 are provided below. Interested and eligible candidates can submit application along with resume.
Vacancy Details:
Intas Recruiting M.Pharma candidates with 00-02 Years Experience for Trainee Research Associate Position.Complete Details for the Trainee Research Associate as follows.
Important Details :
- Location :Ahmedabad
- No of Vacancies: NA
- Details of Salary:NA
- Opening date for online Application:12/12/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
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Job Description/Skills Required
We are looking for candidates with background in pharmacology or toxicology for below roles and responsibilities:
Roles and Responsibilities
- Assist the team leader in various activities related to product development including but not limited to the following:
- Preparation, review and finalization of various regulatory documents such as investigator brochure, non-clinical overview and summary, non-clinical study protocol and report, non-clinical study monitoring, prescribing information, summary of product characteristics
- Interact with cross-functional team to ensure timely completion of assigned activities
- Preparation of documents for regulatory submission related to medical device and combination products
- Literature review to support the product development, query response
Expectations
- Preferred:
- Experience of working in non-clinical and/or clinical development of pharmaceutical drug products,
- Basic understanding of drug development process, regulatory guidelines and processes
- Willingness to work on multiple projects or tasks
- Desirable:
- Knowledge and/or experience of biosimilar development
- Knowledge of various non-clinical and clinical documents such as GLP, toxicity study plan, toxicity study report, non-clinical and clinical overview and summary, investigator brochure, prescribing information, summary of product characteristics
- Knowledge of medical device and importance in pharmaceutical drug development
Click here for Official notification and Apply