Mega Walk-In Interviews for Regulatory Affairs / R&D / AR&D / FR&D / FAR&D on 1st July’ 2023 @ MSN LABS, Hyderabad

Mega Walk-In Interviews for Regulatory Affairs / R&D / AR&D / FR&D / FAR&D on 1st July’ 2023 @ MSN LABS, Hyderabad

MSN Laboratories Pvt. Ltd (MSN Group) is one of the fastest growing manufacturers of Active Pharmaceutical Ingredients (APIs) and Finished dosages in India. Established in the year 2003, MSN Group comprises of eight API manufacturing plants ( including one for Oncology), two finished dosage facility ( one more for Oncology being built) and a dedicated R&D Center and is growing 30-40% every year. Our plants are ISO 9001-2000 certified, WHO: GMP, EU:GMP and USFDA approved. Our manufacturing units are designed to confirm to the principles of Quality, Safety and sound Environment.

ELECTRONIC RECORDS

Walk-in interview for Experienced candidates MSN Laboratories
Build your career with fastest growing Pharma company in India
Date: 1st July 2023
Time: 9:30 AM to 4 PM
Interview Venue: MSN Laboratories pvt ltd, MSN House, Plot no C-24, Sanath Nagar Industrial estate, Sanath Nagar, Hyderabad.

Job Location: MSN R&D Center, Pashamylaram
Departments:

Regulatory Affairs – API

Regulatory Affairs – Formulation

Formulation Analytical Research & Development FAR&D

API Analytical Research & Development AR&D

Formulation Research & Development FR&D

API Research & Development R&D

Candidates with relevant experience in respective department only will be considered

For more Current Opening & Pharma Jobs – Click Here

Job Category: pharma
Job Type: Full Time
Job Location: MSN R&D Center

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Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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