Greetings from
Zenzi Pharmaceutical Industries Private Limited!
Department: QC
Experience: 1-6 yrs
Location: Thane
Qualification: B.Sc / M.Sc / B.Pharm
Job description:
1. GC operation
2. HPLC/FTIR/UV/Dissolution calibration and operation
3. Raw material analysis
4. Finished product /stability analysis
5. Preparation of standard operating procedure ,specification .
6. Change control /deviation /OOS /OOT etc.
7.Review of Analytical Documents .
1. GC operation
2. HPLC/FTIR/UV/Dissolution calibration and operation
3. Raw material analysis
4. Finished product /stability analysis
5. Preparation of standard operating procedure ,specification .
6. Change control /deviation /OOS /OOT etc.
7.Review of Analytical Documents .
Send CV to bhka@zenzi.in
QC in Microbiologist
Experience: 1-4 yrs
Location: Thane, Mumbai
Zenzi
Pharmaceuticals is looking for competent personnel to be an integral part
Educational Qualification: M.Sc /B.Sc in Microbiology / Biotechnology.
Experience: 3-7 Years
Job Location: Tal- Murbad, Dist Thane, Maharashtra
Key role / Responsibility:
1) Media preparation, media stock, Media consumption record & Related Documentation.
2) Growth promotion test of rehydrated media.
3) Daily record of lab and equipment & instrument.
4) Daily PH Meter & balance calibration
5) SOP Preparation.
6) Environmental monitoring of clean room and other controlled area.
7) Water sampling and testing.
8) MLT Test of RM, FP, Bulk, Packing material as per pharmacopeia
9) Sterility test, BET Test, media Fill, BIs test.
10) Master sub culturing and record.
11) Validation of lab equipment & instrument.
12) Area validation and qualification.
13) Validation of autoclave, Incubators & Dry heat sterilizer.
14) Online Documentation with respect to GLP, GDP, GMP.
15) Candidate should have knowledge of pharma regulatory audits.
16) Good communication skill.
17) Should know the USFDA, EU- GMP, MHRA, TGA, audits and other regulatory audits.
Experience: 3-7 Years
Job Location: Tal- Murbad, Dist Thane, Maharashtra
Key role / Responsibility:
1) Media preparation, media stock, Media consumption record & Related Documentation.
2) Growth promotion test of rehydrated media.
3) Daily record of lab and equipment & instrument.
4) Daily PH Meter & balance calibration
5) SOP Preparation.
6) Environmental monitoring of clean room and other controlled area.
7) Water sampling and testing.
8) MLT Test of RM, FP, Bulk, Packing material as per pharmacopeia
9) Sterility test, BET Test, media Fill, BIs test.
10) Master sub culturing and record.
11) Validation of lab equipment & instrument.
12) Area validation and qualification.
13) Validation of autoclave, Incubators & Dry heat sterilizer.
14) Online Documentation with respect to GLP, GDP, GMP.
15) Candidate should have knowledge of pharma regulatory audits.
16) Good communication skill.
17) Should know the USFDA, EU- GMP, MHRA, TGA, audits and other regulatory audits.
Send CV to rolo@zenzi.in
No comments:
Post a Comment