Alembic- interview for Production / Quality (QC/QA) – (API & OSD, Injectables)on 21st July 2024

Alembic- interview for Production / Quality (QC/QA) – (API & OSD, Injectables)on 21st July 2024

Alembic- interview

“Walk In Interviews” organized by Alembic Pharmaceutical Limited at “Vadodara” on 21.07.2024(Sunday) for Production (OSD, Injectables, and API) and Quality-Women Candidates Only (API, OSD, and Injectables) for its Manufacturing sites based near Vadodara.
Job Description:
Qualification: B.Sc./M.Sc./B.E-B.Tech (Chemical Engg.)
Experience: 02-07+years
Department: Production / Quality (QC/QA) – (API & OSD, Injectables)
• Job Location: Vadodara
• Role: Executive / Jr. Executive
Walk-In Interview Details:
Date: 21st July, 2024
Time: 9.30 AM – 3.30 PM
• Venue: Alembic Pharmaceuticals Limited, “Sanskruti Hall” Alembic Colony, Opp. Bhailal Amin General Hospital, Vadodara.
Contact us:
• Production – Email ID: prodform@alembic.co.in
• Production Injectable – Email ID: injectable@alembic.co.in
– QA/QC – Email ID: quality@alembic.co.in
Please Note:
➤ For all the positions, candidates having exposure to regulatory requirements of documentation cGMP/GLP in regulated plants shall be preferred.
➤ Those who are unable to attend the Walk In, may send their updated resume on above provided email-ids respectively.
Please note that Alembic Pharmaceuticals Limited does not hire consultants/agents who promise interviews/jobs for monetary consideration/registration fees. Beware of such fraudulent calls.
http://www.alembicpharmaceuticals.com

Job Category: pharma
Job Type: Full Time
Job Location: - Vadodara Gujarat

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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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