QA Chemist
- Sevalal Enterprises
- 0 to 3 Yrs
- Mumbai
- 5 years ago
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Job Description
Job Description
JD: To review the Batch manufacturing record & B.P.R. after completion of packing Batch. To investigate the market complaint and to maintain the record. To review the stability Protocol .and To conduct the Training Program as per scheduled. Ensuring quality standard for all incoming Material like RM/PM,water air, nitrogen,oxygen, steam etc.pre dispatch inspection and online inspection. Internal Auditing of each dept as per scheduled. and also handling by Q.A. Team customer, FDA, WHO GMP, third party, and Vender audit. Ensure implementation of all SOP with co-ordination with concerned dept. Responsible for CAPA action from customer complaint and other non compliances ,Deviation and out of Specification(oos)Root cause analysis of above . Calibration and validation of all measuring instrument and equipment Machine. Prepare A.P.R.(Annual Product Review) and statical Trend Analysis for the Data. Informing any Non Conforming of product to the Management /Director. Preparation of MFR (Manufacturing Formula Record) for new product or Review product. Batch card issue (BMR) & release and final product release in the absence of QA Head. Interfaced with engineering dept. for preparation of URS/DQ/IQ/FAT/SAT protocols for procurement s & installation. Interfaced with production, Quality Control & Engineering department for protocol preparation & Implementation of validation like- Cleaning Validation/Process Validation/Analytical method Validation / Water Validation. Reduce W.I.P. stock good in the shop floor /finished good stock. To report the daily activities to AGM QA, or Director. Ensuring the Quality of product as per specification.also Ensuring preparation of SOP s for all mfg process of each dept .Validation of Process, analytical Method validation, Machines ,HVAC, Water, Cleaning Validation, Master validation plan , Revalidation incase of any Changes. Risk analysis. Training to Employees for on JOB Training SOPs and Quality Management System GMPs WHO Stanard. Documentation of all quality Record Responsible for housekeeping of plant. Review of environment monitoring and Trading , Review of water system and Trending. Control of all documents MFR,BMR,BPR,and all related document s.Validation of computer system, ERP and Password control QA/QC Carry out vender audit as and when required. To check finished good product in BSR before dispatch. Calculation & Verification of active raw material before manufacturing Product. Art work approval. By checked FDA product permission License. Documentation proper storage such as BMR, Log Sheet , Line Clearance Sheet, Area clean Checklist , Documentation distribution &Retrieval .Control sample collection of each batch of finished good product. Successfully monitored the development of basic requirement of QMS with emphasis on process realization, continual improvement & trend analysis. Started working with scientist for development of Anticancer New Product PacliALL(Protein bounded paclitaxel-Nanoparticle) If you are interested then forward your resume on se*************t@gm**l.com Before you come contact on below no for interview schedule 9561260***/8149881*** E/002 Ground Floor ,Krisha Apt.BuldgNo.-10 Yashwant Srushti,Back Side SaiBaba Temple,Boisar Palghar Road,Boisar (W).8087652***/8983655***/8983920*** Please enroll here : http://www.sevalalplacement.com/new_registration.aspx
Employement Category:
Employement Type: Full timeIndustry: Pharma / Biotech
Role Category: Quality (QA-QC)
Functional Area: Not Applicable
Role/Responsibilies: QA Chemist
Contact Details:
Company Name: Sevalal EnterprisesLocation(s): Mumbai
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₹ 1.0 - 3.0 Lakh/Yr
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Sevalal Job Placement Is located at Navapur Road,Shop No 7, S V Shopping Centre,Navapur Road, Boisar, Thane - ,Opposite Vanjari Samaj Hall,, , Boisar, Mumbai - 401501India's reputed company. our vision and focus to provide customized solutions with quality and cost effective product range. A...
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