Intas Released Job Openings On 07/07/2022.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.Â
Vacancy Details:
Intas Recruiting B.Tech/B.E. in Bio-Chemistry/Bio-Technology,M.Tech,M.Sc Candidates with 03 -07 Years Experience for Executive/Sr-Executive – Manufacturing(Upstream & Downstream) Position.Complete Details for the Executive/Sr-Executive – Manufacturing(Upstream & Downstream) as follows.
Important Details :
- Location :Ahmedabad
- No of Vacancies: 25
- Details of Salary:NA
- Opening date for online Application: 07/07/2022
- 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:Â Laurus Labs Urgent Openings For Diploma,BSc,B.Pharm,M.Pharm,MSc Graduates
Job Description/Skills Required
Position Summary : Responsible for all activities related to Plasma Fractionation process and their compliance as per cGMP requirement
Technical Skill : Column Chromatography, TFF, Filtration, Centrifugation, Process Validation, AKTA Process, , CIP, SIP, QMS
Responsible for all activities related to Plasma Fractionation process and their compliance as per cGMP requirement
- Preparation and review of BPCR, IQ, OQ, PQ Protocols, PV protocols, URS etc.
- Handling of deviations and change controls
- Ensuring cGMP practices in production area
- Handling of SAP activities relating to production.
- Giving training for cGMP practices, equipment handling, manufacturing process to subordinates.
- Review of all written procedures, SOPs, validation protocols, validation reports and other documents.
- Execution of PQ and PV of manufacturing equipment’s test as per protocol
- To co-ordinate with cross functional departments DSP, QA, QC and WH when required to carry out continuous production activities.
- Preparation of purchase requisition, URS, CAPEX and ensuring the availability of Consumables related to swift batch execution.
- Responsible for overall operations of plasma fractionation section
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