About Company:
AET LABORATORIES PRIVATE LIMITED (CIN: U24239TG2003PTC041756) 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:
DEPARTMENT: Technology Excellence
POSITION: Sr. Executive
EXPERIENCE: 6-8 years
QUALIFICATION: M. Pharmacy
JOB DESK:
1.Manage the technology transfer process for established products, ensuring robust and compliant manufacturing processes e.g. implementation of new API sources.
2. Write, review, and maintain regulatory response documents, justification reports, and risk assessments related to technology transfer activities.
3.Oversee the preparation and review of Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) for smooth transfer and manufacturing.
4.Review process validation protocols and reports.
5.Coordinate with R&D, production, quality assurance, and regulatory teams to ensure alignment on project deliverables and timelines..
6.Troubleshoot and optimize manufacturing processes addressing deviations and improving efficiency.
7.Conduct technical risk assessments to identify and mitigate potential issues during and post-transfer.
8.Maintain comprehensive documentation to ensure compliance with regulatory standards (e.g., FDA, EMA, CGMP) and internal quality guidelines.
Looking for your next career move? We’re hiring and would love to hear from you!
How to Apply?
SEND YOUR CV: k.surendra@tiefenbacher.com
Survey No.: 42, Gaddapotharam, Kazipally Industrial Area,
Sanga Reddy Dist. Hyderabad-502319, Telangana, India.
PHONE: +91-841869 4444
