Chemino Pharma Ltd(Shakti Bio Science Ltd) Walk In Interview 2023.Chemino Pharma Ltd(Shakti Bio Science Ltd) Notification full details below..Interested and eligible candidates can attend interview on scheduled time and venue.Chemino Pharma Ltd(Shakti Bio Science Ltd). Is mainly into manufacturing of API & Bulk Drugs. In Business since last 16 Years, company majorly focus on achieving strong foothold in the Indian markets and subcontinents.
Vacancy details:
- Qualification: Quality Assurance AM/ Dy Manager And Manager
- Qualification : MS/M.Sc(Science) in Chemistry
- Experienced: 7 – 12 years
- Salary: 3-7.5 Lacs P.A.
Job Description: Greeting from Chemino Pharma Ltd(Shakti Bio Science Ltd) !!!!
Important Details :
- Location: Vapi
- Post of date:31/08/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Fact to face Interview
- Rounds of Interview: HR
Time and Venue
1st September , 9.30 AM – 4.30 PM
Plot No 411/1,Lic Sector,Silvassa Road,Vapi 396195 Gujarat.
Contact – Harshal Mheta ( 7778955229 )
1)Review of all Specification, Standard Test Procedure, and Batch Process records.
2) Review of Changes that affect the Quality of intermediates or API.
3) Preparation of QA related procedures and documents.
4) Issuance of all kind of documents, SOPs, technical protocols, Validation protocols, specifications, testing procedures, formats and annexure.
5) Reviewing of Validation protocol and reports.
6) Reviewing completed Batch Process records and Analytical records for critical process steps before release of the API for sale.
7) To log in and investigate of Critical Deviations.
8) To log in of Change control and Market complaints
9) To ensure that material are appropriately tested and result are reported.
10) To investigate, resolve and approval Quality related customer complaints.
11) Conducting Self-Inspection internal and external audit customer non-conformities responses.
12) Preparing of annual product Quality review .
13)To coordinate with all the departments with respect to quality and GMP related issue.
15) To initiation and review of all kind of QMS documents
16) Planning and conducting of periodic GMP & departmental training.
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