Dr. Reddy’s Laboratories is Hiring!
- 𝗧𝗲𝗮𝗺 𝗠𝗲𝗺𝗯𝗲𝗿 – 𝗠𝗮𝗻𝘂𝗳𝗮𝗰𝘁𝘂𝗿𝗶𝗻𝗴 𝗤𝗠𝗦 | Injectable Manufacturing
𝗣𝘆𝗱𝗶𝗯𝗵𝗶𝗺𝗮𝘃𝗮𝗿𝗮𝗺, 𝗩𝗶𝘀𝗮𝗸𝗵𝗮𝗽𝗮𝘁𝗻𝗮𝗺, Andhra Pradesh.
𝐊𝐞𝐲 𝐑𝐞𝐬𝐩𝐨𝐧𝐬𝐢𝐛𝐢𝐥𝐢𝐭𝐢𝐞𝐬:
Oversee and ensure cGMP compliance in day‑to‑day production activities
Lead 𝗶𝗻𝗰𝗶𝗱𝗲𝗻𝘁 𝗮𝗻𝗱 𝗱𝗲𝘃𝗶𝗮𝘁𝗶𝗼𝗻 𝗯𝗿𝗮𝗶𝗻𝘀𝘁𝗼𝗿𝗺𝗶𝗻𝗴, 𝗶𝗻𝘃𝗲𝘀𝘁𝗶𝗴𝗮𝘁𝗶𝗼𝗻, 𝗮𝗻𝗱 𝗰𝗹𝗼𝘀𝘂𝗿𝗲
Drive effective 𝗖𝗔𝗣𝗔 𝗶𝗺𝗽𝗹𝗲𝗺𝗲𝗻𝘁𝗮𝘁𝗶𝗼𝗻 and manage 𝗰𝗵𝗮𝗻𝗴𝗲 𝗰𝗼𝗻𝘁𝗿𝗼𝗹 𝗽𝗿𝗼𝗽𝗼𝘀𝗮𝗹𝘀
Review and ensure accuracy of 𝗕𝗠𝗥𝘀, 𝗕𝗣𝗥𝘀, 𝗮𝗻𝗱 𝗲𝗾𝘂𝗶𝗽𝗺𝗲𝗻𝘁 𝗹𝗼𝗴𝗯𝗼𝗼𝗸𝘀.
𝗘𝗹𝗶𝗴𝗶𝗯𝗶𝗹𝗶𝘁𝘆 𝗖𝗿𝗶𝘁𝗲𝗿𝗶𝗮:
𝗤𝘂𝗮𝗹𝗶𝗳𝗶𝗰𝗮𝘁𝗶𝗼𝗻: Diploma / B.Tech in Engineering
𝗘𝘅𝗽𝗲𝗿𝗶𝗲𝗻𝗰𝗲: 4–10 years in sterile manufacturing QMS activities
Strong exposure to cGMP, documentation accuracy, equipment safety, and quality systems.
If you are quality‑driven and looking to grow your career in injectable sterile manufacturing, we’d love to hear from you!
Share your resume at: ravipatitriveni@drreddys.com
Apply here: https://smrtr.io/wXb7N
