Ami Lifesciences-Walk In Interview for RESEARCH & DEVELOPMENT on 01st June’24

Ami Lifesciences-Walk In Interview for RESEARCH & DEVELOPMENT on 01st June’24

Ami Lifesciences-Walk In Interview
RESEARCH & DEVELOPMENT on Saturday, 01st June’24
Roles & Responsibilities:
• Design, finalize and propose specification of KSM, Intermediates and finish API as per developed control strategy.
• Prepare the documents for Process development report and technology transfer.
.
Develop cost effective, high quality and minimum environmental hazardous process considering ICH guideline.
• Finalize the route of synthesis after doing feasibility study of ROS to develop process for DMF filing.
• Lab process development and its optimization with control strategy and Lab validation.
• Literature survey, troubleshooting of plant and Lab scale synthesis, and impurity problems.
Desired Candidate:
M.Sc. Organic Chemistry / Ph.D Chemistry
. 2 to 8 years of experience in API Industry
Venue: Ami Lifesciences Pvt Ltd 2nd Floor, Prestige Plaza 40, Urmi Society, BPC Road, Vadodara
10 AM To 4 PM
Note: Ami Lifesciences does not directly or indirectly charge any fees for job application, processing, training or testing. Do not participate in any such invitations.
Age criteria: 18 or above
Job Location: Karakhadi (Near Vadodara)
Candidate unable to attend the interview can share their profile on careers@amilifesciences.com

Job Category: pharma
Job Type: Full Time
Job Location: Karakhadi (Near Vadodara)

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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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