Opening at Aneta Pharmaceutical for QC, QA, Regulatory Affairs Department

Aneta Pharmaceuticals was established in 2023 as a private company that makes medicines, with a production facility approved by the WHO GMP and the Republic of Uzbekistan, and strict quality control that meets GLP standards. The path of success lies in its belief in creativity and no negotiation with the quality of work.

Opening at Aneta Pharmaceutical Pvt. Ltd. For Below Positions at OSD formulation facility

QA Department
Experience : 2-5 Years
No of post : 1
Area : QA Validation
Post : Officer / Sr. Officer
Qualification : M.Pharm /B.Pharm / M.Sc / B.Sc
Section / Skills : Candidate must have experience in QA Validation

Regulatory Affairs Department
Experience : 0-3 Years
No of post : 2
Area : ROW / EU /CIS Markets
Post : Trainee / Officer
Qualification : B.Pharm / M.Pharm
Section / Skills : Candidate must have experience of CTD/eCTD submissions, and global regulatory guidelines to ensure compliance, timely submissions, and audit-ready documentation, while managing authority queries and partner communications.

Quality Control Department
Experience : 3-5 Years
No of post : 2
Area : FP / IP / RM / PM / QMS/ Doc.
Post : Sr.Officer / Executive / Sr. Executive
Qualification : M.Sc/B.Sc
Section / Skills : Candidate must have experience of Review document of Finish / In-Process, HPLC, UV, Dissolution, DT, Friability, FT-IR Auto titrator, KF, RM / PM etc.

QC - Micro Department
Experience : 3-5 Years
No of post : 1
Area : Micro
Post : Sr.Officer / Executive
Qualification : M.Sc/B.Sc
Section / Skills : Candidate must have experience of Prepared and Review document of Microbiological Testing, Environmental Monitoring, Water Sampling and Analysis, CAPA, Training & Support, Equipment Maintenance, Product Release