Unichem Laboratories-Walk in for M.Pharm, B.Pharm, MSc in QC, Production on 20th to 23rd December 2023

 Unichem Laboratories-Walk in for M.Pharm, B.Pharm, MSc in QC, Production on 20th to 23rd December 2023

Unichem Laboratories Ltd Promoted by the late Mr. Amrut Mody, a pioneer of the Indian pharmaceuticals business, Unichem Laboratories has grown to become one of India’s most respected pharmaceutical companies. It is committed to deliver better health through superior products. By combining strategic research and in-depth industry knowledge, Unichem aims to transform itself into a global pharmaceutical drug Company with an increasing focus on cutting-edge research and developed markets.

Unichem Laboratories Ltd. is looking for young dynamic candidates with ambition and drive for the following departments at our state-of-the-art Pharma Formulations Manufacturing facility at Pilerne Goa

Quality Control
Experience in handling HPLC / GC / UV / IR Spectrometer.

Production
Experience in Oral Solid Dosage Manufacturing / CVC Packaging. Exposure to the latest manufacturing and packing techniques

Qualification – MSC / BSC / MPHARM / BPHARM
Experience – 1 to 6 years (with pharma background)

 

Walk in Interview
Date – 20th December 2023 to 23rd December 2023
Venue – Plot No. 10 to 18, Pilerne Industrial Estate, Pilerne, Pilerne, Bardcz, Goa – 403 511, India.
Timing – 10:00 am -16:00 pm

The candidates willing to work in shift will be given preference.

Freshers and candidates who are unable to attend the interview on the above mentioned date may send their resume to hrgoa@unichemlabs.com

The candidate should bring along updated resume, passport-size photo, all educational certificates previous work experience certificates and current CTC statement

Job Category: pharma
Job Type: Full Time
Job Location: Pilerne Goa

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ABHA

Abha is the Author  of pharmaceutical guidance, she is a pharmaceutical professional having more than 22 years of rich experience in pharmaceutical field. During her career, she works in the quality assurance department with multinational companies i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd. During his experience, she faces many regulatorily audits 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. She is currently leading a regulatory pharmaceutical company as a Head Quality. You can join him by Email, Facebook, Google+, Twitter, and YouTube