Meyer Organics is conducting Walk in drive on 26th August 2021 in Sr. Executive- QA.Welcome to MEYER Organics – India’s one of the leading pharmaceutical manufacturer, founded in 1982 in technical collaboration with OMEGA – MEYER Ltd., Jersey ( Br. Isles). Interested and eligible candidates can attend interview on scheduled time and venue.
Walk in Details :
- Company Name: Meyer Organics
- Location : Bengaluru
- Post Name: Sr. Executive- QA
- Qualification:B.Pharmacy/M.Pharmacy
- Experience: 02-06 Years
- No of Vacancies: NA
- Details of Salary: ₹ 2,00,000 – 4,00,000 P.A.
- Time And Venue: 26 August , 9.30 AM – 5.30 PM
Meyer Organics Pvt. Ltd. No. 10 D, 2nd Phase, Peenya Industrial Area, Bangalore – 560058. Land Mark- Southern Gas Factory
- Contact: Divya ( 9945544952 )
- Email: NA
- Selection Process: Based on interview
Job Description/Skills Required.
1. Line clearance ( Liquid Oral , Tablets , Capsules)
2. Responsible for monitoring In-process quality control checks in manufacturing department.
3. Comparing the description for all products against the standards.
4. Collection of samples stage wise for analysis and handover for QC Testing.
5. Checking any OOS recorded during online process and reporting to seniors.
6. Final BMR reconciliation before release for packing.
7. Preparation of Process Validation protocol & Flow charts of Tablets.
8. Preparation of presentation of products that are manufactured as a part of training.
9.To stop the line in case of any non compliance and with proper approval and guidance from seniors and HOD.
10.To reconcile the BMR and handover the final BMR for closure.
REGULATORY
- Handling of documents for Export / Import NOCs.
- Handling of documents for Additional Product Permissions.
- Handling of documents for Certifications GMP, CoPP, FSC, NC, Capacity, Market Standing, GLP, Test Licence, CTS.
- Knowledge about online portals of DCGI / SLA – SEVASINDHU / IDMLA / e-SUGAM.
- Handling of documents for FSSAI licensing and Certifications with State FSSAI & Central FSSAI.
- Handling of documents for WHO-GMP application and certifications.
- Reviewing Stability / Validation protocols and reports.
