- Work in a company with a solid track record of performance
- Opportunity to make a positive impact
- Flexible working options
- Daily Calibration of instruments like pH meter, Analytical Balance, HPLC, GC, etc.
- Audit trail review of computer systems in instruments like HPLC, GC, KF, and IR.
- Timely approval of Raw Materials, Packing Materials and Finish Products with accurate analysis.
- Handling of Out of Specification (OOS).
- Review of Documents such as BMR, SOPs, STPs, Validation Docs, and QC Analytical Documents.
- Preparation and checking of Cleaning validation analytical reports.
- Experience in IPQC, 21 CFR, Change Control, Deviation Management, documentation and approval wherever required.
- Investigating Market complaints and Responding to customers on time.
- Vendor Audits and vendor qualification as per SOP requirements
- APQR preparation and review.
- Preparation of SOP for the QA department
- Preparation of COAs and customer samples packing
- Review of other department documents that are submitted to the Quality assurance department and review analytical data of Raw material, packing material, semi-finished and finished products before release.
- Handling the sampling, control sample management, and handling the hold time stability study data.
- Making the module presentation of training as per SOP/schedule. Assist with internal audit activity and its compliance.
- You have at least 3 years experience including solid experience in a similar role within Industrial and Healthcare & Lifesciences.
- Hands on experience in Instrumentation like HPLC, GC, UV, IR etc. (Shimadzu)
- Qualified M.Sc. Chemistry
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QA Officer - Kalyan, India - Snaphunt
Description
The Offer
The Job
You will be responsible for :
The Profile
The Employer
Our client is a pharmaceutical and healthcare ingredient & intermediate company and the first manufacturer of saccharin and its salts (artificial sweeteners) in India