Avenza operates its pharmaceuticals manufacturing facilities at Vadodara Gujarat India. The manufacturing unit is a developing comprehensive unit which combines production, sales, research & development as a whole. The company has state-of-the-art manufacturing along with an ultra advanced analytical lab system.
We are looking for young and Dynamic Professional from Pharmaceuticals (OSD Formulation) Background with proven track record, who have exposure to advance/regulated market operations (USFDA/MHRA/TGA/EU-GMP) for Tablets (General & Effervescent) Capsules, Suppositories.
Vacancy in QC Department
Stability
Role and No of post : Analyst ; 01
Experience : 3 to 5 years
Job Description : Stability sample testing. HPLC/UV/IR and chemical testing experience Summary preparation. Knowledge about stability sample management.
AMV
Role and No of post : Analyst ; 02
Experience : 5 to 7 years
Job Description : HPLC/UV/IR and chemical testing. Must have method validation experience.
Process validation/ FP/ln process
Role and No of post : Analyst ; 02
Experience : 3 to 5 years
Job Description : HPLC/UV/IR and chemical testing
Process validation/ FP/AMV/Stability
Role and No of post : Reviewer ; 02
Experience : 8-10 Years
Job Description : Must have experience in handling of HPLC/UV/IR/GC. Knowledge about review of audit trail of instrument. Should know the method validation process and stability management.
QMS
Role and No of post : Documentation/ QMS ; 01
Experience : 05 to 07 years
Job Description : SOP revision/STP, SPEC, TDS revision/ Validation protocol report. QMS report
Microbiology
Role and No of post : Documentation/ reviewer/QMS ; 01
Experience : 3 to 5 years
Job Description : SOP revision/STP, SPEC, TDS revision/ Validation protocol report. QMS report
Location : Jarod, Samlaya, Vadodara
Send your updated resume to : recruitment@avenzapharma.com
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Subject Line : Application for QC
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