Otsuka Pharmaceutical – Walk-In Interviews on 23rd Sep’ 2023

Otsuka Pharmaceutical – Walk-In Interviews on 23rd Sep’ 2023

About

 Otsuka

Otsuka Pharmaceutical was established in 1964.
At Otsuka Pharmaceutical, we are committed to a holistic approach to the health and well-being of people and are striving to create innovative, thoroughly original pharmaceutical and nutraceutical products based on our corporate philosophy
"Otsuka-people creating new products for better health worldwide".

Otsuka Pharmaceutical India Private Limited (OPI) is a Joint Venture between Otsuka Pharmaceutical Factory, Inc., Japan, and Mitsui & Co. Ltd., Japan, for Infusion Business in India and Emerging Markets. We primarily manufacture & market products across multiple markets and therapeutic segments. As a leader in intravenous nutrition products, we are committed to being the best partner for patients and healthcare professionals in clinical nutrition...

 

Otsuka Pharmaceutical Walk-in-Interview

• Qualification: B.Pharm, M.Pharm
• Experience: 02-07+years
• Department: Regulatory Affairs
• Job Location: Ahmedabad
• Role: Process In charge
• Salary: 3-6 Lacs P.A.
• No. of Openings: 03

Time and Venue:

23 September 9.00 AM – 2.00 PM

Otsuka Pharmaceutical India Pvt. Ltd., 21st Floor, B Block, Westgate, near YMCA Club, SG Highway, Ahmedabad-380015, Gujarat. Tele. – 079-66216000

Contact – Himanshu (7984556557)

 

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Job description:

Role & responsibilities:

• Dossier preparation/review as per the country-specific guideline/CTD guideline
• Timely query response submission to Distributor/ MOH
• Review of documents for their correctness and compliance with respective regulatory guidelines (as per country requirement)
• Preparation, review & release of artworks & sales order as per country approval
• Variation documents preparation and filing as per country requirements
• Timely dispatch of tender documents to country/parties as per deadline

Preferred candidate profile:

• Should be able to review & interpret the requirement as per country-specific/ tender guideline
• Should be able to review various plant documents for dossier preparation like Process validation, Stability study, PDR, Method validation, SOP, Drug Master File, BMR, APR, etc.
• Should be able to handle a team of two members
• Should be able to communicate with relevant functions for procurement of required regulatory documents
• Should be able to communicate with relevant counterparts at country
• Preferred Immediate joiners

 

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