Glenmark-Interview for Production/Packing/ Semi Solid on 25th Feb 24

Glenmark-Interview for Production/Packing/ Semi Solid on 25th Feb 24

Glenmark-Interview

Walk-In Production/Packing/ Semi Solid
 Glenmark
at Sikkim for Glenmark Pharmaceuticals ltd., Goa
Senior Officer-Production/Packing/Semi Solid Production:

Capsule, Compression and Coating
Packing: Bottle/Blister
Semi Solid: SSD Manufacturing
Qualification: Regular (Full Time) B.Pharm/M.Pharma
Experience: 2 to 6 Years
Officer-Production/Semi Solid
Production: Granulation, Compression,Coating, Wruster/Pellet Coating. Capsule Filling, Inspection
Semi Solid: SSD Packing, SSD Manufacturing & Tube Filling
Qualification: Regular (Full Time) Diploma / B. Com/B.A./B.Sc. Experience: 2 to 6 Years
Junior Officer – Production/Semi Solid
Production: Granulation, Compression,Coating, Wruster/Pellet Coating, Capsule Filling, Inspection
Semi Solid: SSD Packing, SSD Manufacturing & Tube Filling
Qualification: Regular (Full Time) ITI or HSSC with at least 5 Years Relevant Experience
Experience: 2 to 6 Years
Walk-In on 25th Feb 24 (Sunday)
09:00 AM-06:00 PM
Venue: Eco Paradise Resort
NH 10, Rangpo Mining, Gangtok Road East – Sikkim
Contact HR Person : Mr. Vithal Hebbalkar
You can also e-mail your resume on Aditi.Narvekar@glenmarkpharma.com if you are not able to participate in the walk-in
Kindly Carry the below documents for verification on the Date of Interview:
1) Recent Passport size photo 2) Academic & Employment Certificates 3) PAN Card & Aadhar
Please Note: Glenmark does not collect any fees or charges, directly or through any agency, from candidates or any other person or entity for securing employment in the company

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

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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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