Glenmark Pharmaceuticals-Interview for Multiple Positions on 23rd – 29th June’ 2024

Glenmark Pharmaceuticals-Interview for Multiple Positions on 23rd – 29th June’ 2024

Glenmark Pharmaceuticals-Interview

Jr. Officer / Officer / Sr. Officer – Production (Semi Solid Dosage)

Responsibilities:

SS Manufacturing & Filling

Packing

SS Manufacturing

T&T Machine Operation

Labelling Machine Operation

Cartonator Machine Operation

SS Filling

Qualification: Diploma / ITI / B.Pharmacy

Experience: Minimum 4 years

Jr. Officer / Officer / Sr. Officer – Production (Oral Solid Dosage)

Responsibilities:

Granulation

Compression

Capsule Filling

Coating

Qualification: Diploma / B.Pharmacy

Experience: Minimum 2 to 4 years

QC Analyst / Reviewer / Supervisor – Quality Control

Responsibilities:

Finished Goods (FG) Quality Control

Stability Testing

Lab Support

Quality Management System (QMS)

Qualification: B.Sc / M.Sc

Experience: Minimum 3 to 6 years

Interview Details:

Dates: 23rd June 2024 – 29th June 2024

Time: 02:00 PM – 5:00 PM

Venue: Glenmark Pharmaceuticals Limited, Plot No. 2, Phase II, Pharma Zone, ISEZ, Pithampur, Indore M.P, 454775

Requirements:

Candidates must have experience in pharmaceutical units approved by regulatory agencies such as USFDA, MHRA, etc.

How to Apply: Interested candidates are invited to send their resumes to Priyanka Narwani at Priyanka.narwani@glenmarkpharma.com.

Job Category: pharma
Job Type: Full Time
Job Location: Indore M.P Pithampur

Apply for this position

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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