Dr. Reddys Laboratories Released Job Openings On 14/05/2022. Dr. Reddy€™s Laboratories Ltd. (NYSE: RDY) is an integrated global pharmaceutical company, committed to providing affordable and innovative medicines for healthier lives. Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Dr. Reddys Laboratories Recruitment 2022 are provided below. Interested and eligible candidates can submit application along with resume.
Vacancy Details:
Dr. Reddys Laboratories Recruiting M.Sc with 4+ Years of relevant Experience for Research Scientist Position.Complete Details for the Research Scientist as follows.
Important Details :
- Location : Hyderabad
- No of Vacancies:NA
- Details of Salary: NA
- Opening date for online Application: 14/05/2022
- 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
Related Job: Email Resume : Macleods Pharmaceuticals Recruiting B.Pharma,M.Pharma,M.Sc Graduates
For more Latest pharma jobs https://pharmapage.in/
Job Description/Skills Required
- Execution of method transfer/ method validation between QC and IPDO/ASAT for New and Tech transfer products.
- Execution of validations as per Protocol and complies to current SOP requirements.
- Review of analytical method development reports before initiation of method validation study and understand the criticality of each method.
- Ensuring all pre requisites before initiation of method validation , transfer activities.
- Preparation of Analytical method transfer protocols as per need.
- Preparation of justification reports, AMV protocols, Reports as per the need.
- Responsible to investigate analytical method issues during the method transfer/validation execution
- Coordinate with AQA/QA to get all document review and approvals on time.
- Participating in all the analytical investigations to identify the root cause and implement appropriate corrective and preventive actions.
- Execution of deficiency related analysis as per protocol.
- Analysis of Trial/ Confirmatory batch analysis as per protocol.
- Ensuring Safety practices at work place.
- Maintenance of laboratory as per the cGLP.
- Having the good documentation skill
- Getting trained for all the instruments and SOPs on time.
- Supporting for all audits at Plant
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