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| Job Location | Mumbai City |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Pharma / Biotech |
| Functional Area | uality (QA-QC) |
| EmploymentType | Full-time |
Dear All,We have vacancy for B.Pharm Fresher in QA / PRODUCTION Dept in Boisar / Palghar Location.Qualification - B.pharm /M.PharmJob Location - Boisar / PalgharInterested candidates can mail your resume on sevalal777@yahoo.com or Directly attain interview on 22/03/2019 to 23/03/2019.JD:Line clearance, Dispatch of finished material, Cleanliness checking as per cGMP & regulatory requirements & guidelines. Checking all submitted BMRs,BPRs,ECRs for completion with all attached documents. Material code generation form & master label form issuance & distribution of controlled copies to respective departments. Tracking Product details list & related documents record in soft & hard copies. (validation & commercial batches files for audit purpose). Updating stability data by coordinating with analytical QA in APQR excel sheet & preparation of related graphs. Issuance: Keeping MASTER LIST & approved vendors record of raw materials & distribution of controlled copies to respective departments. Issuance of Logbooks, forms & archival retrieval of same in regulated environment. Revised SOP distribution, retrieval & destruction of old versions controlled copies & tracking all master versions record. Numbering of Logbooks, Workbooks & Registers. Handling of master documents (PDR,PVP,PVR,CVP,CVR,TTP,TTR,IQ,OQ,PQ) & controlled copies archival, retrieval, destruction activity as per SOP. AWS issuance for analysis for QC department within stipulated time. Document entry & reporting, accurate & timely data collection, keeping track of Obsolete documents & destruction of retrieval. Regulatory work: Collecting & providing required documents copies (BMRs, AMV reports, vendor as well as site COAs of raw materials & FP, Declarations, Yield data, vendor qualification) to RA & Corporate office as per requirement. Audit Support: Customer & USFDA document providing within Auditors time frame. Making files arrangement with proper labelling and numbering for identification and tracking purpose. USFDA Audit passed with zero 483 & expected Compliance. Training: ensuring all departments are completing their trainings within due date. Keeping records of all training documents such as assessments & attendance sheets in system (scan) and hard copy format also. To maintain 100 % compliance related to training.FOR FURTHER DETAILS KINDLY CONTACT:8149881777/ 9561260777/9765920777/8087652777Best Regards,Miss. Seema PatelContact : 8149881777/ 9765920777H.R & Admin.SEVALAL JOB PLACEMENTE/002 Ground Floor, Krisha Apt.Buldg No.-10, Yashwant Srushti,Back Side Sai Baba Temple,Boisar Palghar Road, Boisar (W).8087652777/8983655777/8983920777
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