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PHARMA JOBS POST > Graviti Pharma Hiring QA Validation (OSD) | Assistant Manager / Deputy Manager Jobs Hyderabad

Graviti Pharma Hiring QA Validation (OSD) | Assistant Manager / Deputy Manager Jobs Hyderabad

Apply for QA Validation jobs at Graviti Pharma, Hyderabad. Hiring Assistant Manager / Deputy Manager for OSD formulation with experience in cGMP, validation & qualification.

ADMIN
Last updated: April 3, 2026 4:29 am
ADMIN 4 weeks ago
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Graviti Pharma Hiring QA Validation Professionals
Graviti Pharma Hiring QA Validation Professionals
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  • 𝗜𝘀𝗻𝗮𝗽𝘂𝗿, 𝗛𝘆𝗱𝗲𝗿𝗮𝗯𝗮𝗱
  • Posted 4 weeks ago
Graviti Pharma

Graviti Pharma

Graviti Pharma Hiring QA Validation Professionals

Graviti Pharma is hiring experienced professionals for Quality Assurance – Validation (OSD Formulation) roles at its Hyderabad facility. This is an excellent opportunity for candidates with strong expertise in validation and qualification activities to grow their careers in the pharmaceutical industry.

𝗪𝗲 𝗔𝗿𝗲 𝗛𝗶𝗿𝗶𝗻𝗴 – 𝗤𝘂𝗮𝗹𝗶𝘁𝘆 𝗔𝘀𝘀𝘂𝗿𝗮𝗻𝗰𝗲 – 𝗩𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 (𝗢𝗦𝗗 𝗙𝗼𝗿𝗺𝘂𝗹𝗮𝘁𝗶𝗼𝗻)

📌 𝗗𝗲𝘀𝗶𝗴𝗻𝗮𝘁𝗶𝗼𝗻: 𝗔𝘀𝘀𝗶𝘀𝘁𝗮𝗻𝘁 𝗠𝗮𝗻𝗮𝗴𝗲𝗿 / 𝗗𝗲𝗽𝘂𝘁𝘆 𝗠𝗮𝗻𝗮𝗴𝗲𝗿
📍 𝗟𝗼𝗰𝗮𝘁𝗶𝗼𝗻: 𝗜𝘀𝗻𝗮𝗽𝘂𝗿, 𝗛𝘆𝗱𝗲𝗿𝗮𝗯𝗮𝗱
🏢 𝗗𝗲𝗽𝗮𝗿𝘁𝗺𝗲𝗻𝘁: 𝗤𝘂𝗮𝗹𝗶𝘁𝘆 𝗔𝘀𝘀𝘂𝗿𝗮𝗻𝗰𝗲 – 𝗩𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻

We are actively looking for professionals with strong experience in 𝗢𝗦𝗗 (𝗢𝗿𝗮𝗹 𝗦𝗼𝗹𝗶𝗱 𝗗𝗼𝘀𝗮𝗴𝗲) formulation within 𝗤𝗔 𝗩𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 at Graviti Pharma.  If you have strong exposure to validation and qualification activities in the pharmaceutical industry, this is a great opportunity to advance your career

🔹 𝗞𝗲𝘆 𝗥𝗲𝘀𝗽𝗼𝗻𝘀𝗶𝗯𝗶𝗹𝗶𝘁𝗶𝗲𝘀:
• 𝖤𝗇𝗌𝗎𝗋𝖾 𝖼𝗈𝗆𝗉𝗅𝗂𝖺𝗇𝖼𝖾 𝗐𝗂𝗍𝗁 𝖦𝗈𝗈𝖽 𝖣𝗈𝖼𝗎𝗆𝖾𝗇𝗍𝖺𝗍𝗂𝗈𝗇 𝖯𝗋𝖺𝖼𝗍𝗂𝖼𝖾𝗌 (𝖦𝖣𝖯), 𝖼𝖦𝖬𝖯 & 𝖰𝗎𝖺𝗅𝗂𝗍𝗒 𝗉𝗈𝗅𝗂𝖼𝗂𝖾𝗌
• 𝖯𝗋𝖾𝗉𝖺𝗋𝖺𝗍𝗂𝗈𝗇, 𝗋𝖾𝗏𝗂𝖾𝗐, 𝖺𝗉𝗉𝗋𝗈𝗏𝖺𝗅 & 𝖾𝗑𝖾𝖼𝗎𝗍𝗂𝗈𝗇 𝗈𝖿 𝗉𝗋𝗈𝖼𝖾𝗌𝗌, 𝖼𝗅𝖾𝖺𝗇𝗂𝗇𝗀, 𝗉𝖺𝖼𝗄𝗂𝗇𝗀 𝗏𝖺𝗅𝗂𝖽𝖺𝗍𝗂𝗈𝗇 & 𝗁𝗈𝗅𝖽 𝗍𝗂𝗆𝖾 𝗌𝗍𝗎𝖽𝗂𝖾𝗌
• 𝖧𝖺𝗇𝖽𝗅𝗂𝗇𝗀 𝖾𝗊𝗎𝗂𝗉𝗆𝖾𝗇𝗍, 𝗎𝗍𝗂𝗅𝗂𝗍𝗂𝖾𝗌, 𝖿𝖺𝖼𝗂𝗅𝗂𝗍𝗒, 𝗂𝗇𝗌𝗍𝗋𝗎𝗆𝖾𝗇𝗍 & 𝗌𝗈𝖿𝗍𝗐𝖺𝗋𝖾 𝗊𝗎𝖺𝗅𝗂𝖿𝗂𝖼𝖺𝗍𝗂𝗈𝗇 𝖺𝖼𝗍𝗂𝗏𝗂𝗍𝗂𝖾𝗌
• 𝖱𝖾𝗏𝗂𝖾𝗐 & 𝖺𝗉𝗉𝗋𝗈𝗏𝖺𝗅 𝗈𝖿 𝖦𝖬𝖯 𝖽𝗈𝖼𝗎𝗆𝖾𝗇𝗍𝗌 (𝖲𝖮𝖯𝗌, 𝗉𝗋𝗈𝗍𝗈𝖼𝗈𝗅𝗌, 𝗋𝖾𝗉𝗈𝗋𝗍𝗌, 𝖽𝗋𝖺𝗐𝗂𝗇𝗀𝗌, 𝗅𝖺𝗒𝗈𝗎𝗍𝗌, 𝖾𝗍𝖼.)
• 𝖯𝗋𝖾𝗉𝖺𝗋𝖺𝗍𝗂𝗈𝗇 & 𝖺𝗉𝗉𝗋𝗈𝗏𝖺𝗅 𝗈𝖿 𝖲𝖬𝖥, 𝖵𝖬𝖯 & 𝗋𝖾𝗊𝗎𝖺𝗅𝗂𝖿𝗂𝖼𝖺𝗍𝗂𝗈𝗇 𝖽𝗈𝖼𝗎𝗆𝖾𝗇𝗍𝗌
• 𝖳𝖾𝗆𝗉𝖾𝗋𝖺𝗍𝗎𝗋𝖾 𝗆𝖺𝗉𝗉𝗂𝗇𝗀, 𝖯𝖬𝖯 𝗋𝖾𝗏𝗂𝖾𝗐 & 𝗏𝖺𝗅𝗂𝖽𝖺𝗍𝗂𝗈𝗇 𝗅𝗂𝖿𝖾𝖼𝗒𝖼𝗅𝖾 𝗆𝖺𝗇𝖺𝗀𝖾𝗆𝖾𝗇𝗍
• 𝖧𝖺𝗇𝖽𝗅𝗂𝗇𝗀 𝖽𝖾𝗏𝗂𝖺𝗍𝗂𝗈𝗇𝗌, 𝖼𝗁𝖺𝗇𝗀𝖾 𝖼𝗈𝗇𝗍𝗋𝗈𝗅𝗌 & 𝖢𝖠𝖯𝖠 𝗋𝖾𝗅𝖺𝗍𝖾𝖽 𝗍𝗈 𝗏𝖺𝗅𝗂𝖽𝖺𝗍𝗂𝗈𝗇
• 𝖯𝖺𝗋𝗍𝗂𝖼𝗂𝗉𝖺𝗍𝗂𝗈𝗇 𝗂𝗇 𝖥𝖠𝖳 / 𝖲𝖠𝖳 𝖺𝖼𝗍𝗂𝗏𝗂𝗍𝗂𝖾𝗌
• 𝖯𝗋𝖾𝗉𝖺𝗋𝖺𝗍𝗂𝗈𝗇 𝗈𝖿 𝖯𝗋𝗈𝖽𝗎𝖼𝗍 𝖰𝗎𝖺𝗅𝗂𝗍𝗒 𝖱𝖾𝗏𝗂𝖾𝗐 (𝖯𝖰𝖱) & 𝖢𝗈𝗇𝗍𝗂𝗇𝗎𝗈𝗎𝗌 𝖯𝗋𝗈𝖼𝖾𝗌𝗌 𝖵𝖾𝗋𝗂𝖿𝗂𝖼𝖺𝗍𝗂𝗈𝗇 (𝖢𝖯𝖵)
• 𝖢𝗈𝗇𝖽𝗎𝖼𝗍 𝗍𝗋𝖺𝗂𝗇𝗂𝗇𝗀 𝗌𝖾𝗌𝗌𝗂𝗈𝗇𝗌 & 𝖾𝗇𝗌𝗎𝗋𝖾 𝖼𝗈𝗆𝗉𝗅𝗂𝖺𝗇𝖼𝖾 𝖺𝖼𝗋𝗈𝗌𝗌 𝖽𝖾𝗉𝖺𝗋𝗍𝗆𝖾𝗇𝗍𝗌

🔹 𝗖𝗮𝗻𝗱𝗶𝗱𝗮𝘁𝗲 𝗣𝗿𝗼𝗳𝗶𝗹𝗲:
✔ 𝖲𝗍𝗋𝗈𝗇𝗀 𝖾𝗑𝗉𝖾𝗋𝗂𝖾𝗇𝖼𝖾 𝗂𝗇 𝖰𝖠 𝖵𝖺𝗅𝗂𝖽𝖺𝗍𝗂𝗈𝗇
✔ 𝖦𝗈𝗈𝖽 𝗎𝗇𝖽𝖾𝗋𝗌𝗍𝖺𝗇𝖽𝗂𝗇𝗀 𝗈𝖿 𝖼𝖦𝖬𝖯, 𝖦𝖣𝖯 & 𝗋𝖾𝗀𝗎𝗅𝖺𝗍𝗈𝗋𝗒 𝗋𝖾𝗊𝗎𝗂𝗋𝖾𝗆𝖾𝗇𝗍𝗌
✔ 𝖤𝗑𝗉𝖾𝗋𝗂𝖾𝗇𝖼𝖾 𝗂𝗇 𝖽𝗈𝖼𝗎𝗆𝖾𝗇𝗍𝖺𝗍𝗂𝗈𝗇, 𝗊𝗎𝖺𝗅𝗂𝖿𝗂𝖼𝖺𝗍𝗂𝗈𝗇 & 𝗋𝗂𝗌𝗄 𝖺𝗌𝗌𝖾𝗌𝗌𝗆𝖾𝗇𝗍

📩 𝖨𝗇𝗍𝖾𝗋𝖾𝗌𝗍𝖾𝖽 𝖼𝖺𝗇𝖽𝗂𝖽𝖺𝗍𝖾𝗌 𝖼𝖺𝗇 𝗌𝗁𝖺𝗋𝖾 𝗍𝗁𝖾𝗂𝗋 𝗋𝖾𝗌𝗎𝗆𝖾𝗌 𝖺𝗍: 𝗅𝖺𝗑𝗆𝗂𝗄𝖺𝗇𝗍𝗁𝗀𝗈𝗎𝖽.𝖾@𝗀𝗋𝖺𝗏𝗂𝗍𝗂𝗉𝗁𝖺𝗋𝗆𝖺.𝖼𝗈.𝗂𝗇 , 𝗁𝗋@𝗀𝗋𝖺𝗏𝗂𝗍𝗂𝗉𝗁𝖺𝗋𝗆𝖺.𝖼𝗈𝗆

To apply for this job please visit 𝗀𝗋𝖺𝗏𝗂𝗍𝗂𝗉𝗁𝖺𝗋𝗆𝖺.𝖼𝗈𝗆.

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Sanyasi Pradhan, M.Pharm, is a pharma professional and entrepreneur with a strong background in the pharmaceutical industry, writing on jobs and global pharma updates
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