Intas Released Job Openings On 01/09/2022.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.Sc. or B.Tech / M.Tech in Biotechnology / Microbiology/Biochemistry / Life Sciences) candidates with 02-06 Years Experience for EXECUTIVE / SR. EXECUTIVE – QA QMS Position.Complete Details for the EXECUTIVE / SR. EXECUTIVE – QA QMS as follows.
Important Details :
- Location :Ahmedabad
- No of Vacancies: NA
- Details of Salary:NA
- Opening date for online Application: 01/09/2022
- 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: FRESHER Openings At Ishita Drugs & Industries Ltd
Job Description/Skills Required
- Participate in Change control and CAPA management, change control and CAPA review, coordinate with stakeholders, experience in electronic system of QMS.
- Participate in Process Performance qualification (PPQ), assist in review documents generated during the PPQ. To provide required support for execution of PPQ, training and successful completion of PPQ
- Participate in cleaning validation and verification exercise, provide necessary input wherever required. Review and verification validation, monitoring the activity data as part validation and verification.
- Review and assessment of Deviation investigation, OOS/OOT investigation. Participate in cross functional discussion of investigations. Training to staff on investigation write up and expectation.
- Coordinate with relevant stakeholder in QA for APQR preparation and review. Ensuring the recommendations are implemented successfully.
- Participate in Continuous Continued Process Verification (CPV) program. Provide necessary inputs for implementation and monitoring. Part of implementation team to verify the product life cycle. Review of CPV protocols and reports
- Review the study protocols, evaluation reports, risk assessment etc.
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