About Company:
AET LABORATORIES PRIVATE LIMITED is a Private company incorporated on 24 Dec 2003. It is classified as Non-government company and is registered at Registrar of Companies, Hyderabad. Its authorized share capital is Rs. 150000000.00 and its paid up capital is Rs. 81778820.00.
AET LABORATORIES PRIVATE LIMITED’s Annual General Meeting (AGM) was last held on 29 Dec 2023. and as per records from Ministry of Corporate Affairs (MCA), its balance sheet was last filed on 2023-03-31.AET LABORATORIES PRIVATE LIMITED’s NIC code is 2423 (which is part of its CIN). As per the NIC code, it is inolved in Manufacture of pharmaceuticals, medicinal chemicals and botanical products.
Directors of AET LABORATORIES PRIVATE LIMITED are KRISTIAN PHILIP RUEPP, SWAPNIL SINGH, OLIVER ROBERT ALEXANDER SCHRADER, DR GEORG STARK, and DIETER SCHOENFELD.
AET LABORATORIES PRIVATE LIMITED’s Corporate Identification Number (CIN) is U24239TG2003PTC041756 and its registration number is 41756. Users may contact AET LABORATORIES PRIVATE LIMITED on its Email address – swapnil.s@aet.in. Registered address of AET LABORATORIES PRIVATE LIMITED is Survey No.42, Gaddapotharam, Kazipally Industrial Area, , SANGAREDDY, Telangana, India – 502319.
Vacancy Details:
Job description:
TIEFENBACHER AET LABORATORIES
WE’RE HIRING
JOIN OUR TEAM!
DEPARTMENT: Quality Assurance (DQA)
EXPERIENCE: 08 to 14 years
DESIGNATION: Asst. Manager, Dy. Manager, Manager levels
QUALIFICATION: M. Pharmacy / B. Pharmacy
JOB SKILL:
1.Responsible for review and approval of Process development documents like Master Product Card, Reference Formula Card, Study medication batch records, Product development reports & Batch selection reports.
2.Responsible for impact assessment & coordination of Change controls and Deviations of Analytical and Product Development Laboratories.
3.Responsible for review of audit trials in Analytical Development Laboratory.
4.Responsible for review of documents and support for submission
of dossiers/ CTD.
5.Responsible for compilation of Technical Data Package, Nitrosamine Risk Assessment and ICH Q3D elemental impurities risk assessments.
6.Responsible for review of OOS/ OOT and Incidents annual summary reports.
7.Responsible for review of SOP’s and Formats related to Quality Assurance, R&D activities.
8.Responsible for review of Process development documents like Master Product Card, Reference Formula Card, Study medication batch records, Product development reports & Batch selection reports.
k.surendra@tiefenbacher.com
www.tiefenbacher-pharmaceuticals.com
