Softgel Healthcare Pvt. Ltd Walk-in Interview 2023.Softgel Healthcare Pvt. Ltd Notification full details below.Interested and eligible candidates can attend interview on scheduled time and venue.Softgel Healthcare provides Outsourcing Solutions to the Pharmaceuticals and Nutraceuticals industry. The company, an associate of the reputed Madras Pharmaceuticals, and has recently set up its state of art and dedicated encapsulation facility for manufacture of soft gelatin capsules.
Vacancy details:
- Designation: Sr. Chemist/ Executive/ Sr. Executive
- Department: – QA / QC & AD
- Qualification: M.Sc / B.Pharm / M.Pharm / B.Tech – Biochem, Biotech, Biomedical
- Experienced:2 +7 yrs
- Openings: 10
Job Description: Greeting from Softgel Healthcare Pvt. Ltd !!!
Important Details :
- Location: Chennai (Kelambakkam)
- Post of date:09/08/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face
- Interview Rounds of Interview: HR
Walk-in Interview Detail Softgel Healthcare Pvt. Ltd
Date: 10th August – 13th August, 2023
Time: 9.30 AM – 4.00 PM
Venue: Softgel Healthcare Pvt. Ltd, Survey No:20/1, Vandalur – Kelambakkam Road, Pudupakkam Village – 603 103, Tamil Nadu.
Phone: +91 73732 51777, +91 73732 52777,
Email: career@softgelhealthcare.com
Quality Assurance:
- Monitoring the compliance of cGMP in warehouse, manufacturing and packing areas
- To verify the functioning of QA systems on the shop floor during shift hours
- Monitoring the Dispensing, manufacturing activities as per GMP requirements
- Performing In process checks of manufacturing and packing activities as per the approved batch document record/ Batch manufacturing record and Batch packing record appropriately to ensure product quality
- Sampling at different stages of manufacturing and packaging activity
- Giving line clearance for the dispensing, manufacturing and packing
- Ensuring cleanliness and traces of batch/ material/ product as applicable.
- Preparing, Issuing, Monitoring and maintenance of BMR/BPR/BDR.
- Preparation of Annual Product Quality Review.
AD
- Maintenance of Laboratory Log books and documents
- Developing of new methods and documentation of the same.
- Summarization of stability data.
- Review of Analytical method validation, Analytical method transfer and Comparative dissolution profile.
- Maintenance of Column stocks and usage log book.
- Review of Method Development (New product formulation) documents.
- Review and Summarize the Stability data.
- Support to regulatory queries.
- Periodic Calibration and performance verification and preventive maintenance of HPLC, GC, dissolution apparatus.
Quality Control
- Should prepare and review SPEC/MOA/ATR/ADS/GTP.
- Should ensure proper care of colums, working Standards.
- Responsible for testing of In- process/ Bulk Products/ Finished Products.
- Documentation of all analysis performed
- Handling QC related instruments.
- Should analyse raw materials/stability samples/process validation.
- Periodic Calibration and performance verification and preventive maintenance of HPLC, GC, dissolution apparatus.
- Should ensure proper labelling of reagents, glasswares, mobile phase etc.
