Mangalam Drugs & Organics-openings for Production, QA, CQA, IPQA, Engineering & Maintenance departments

Mangalam Drugs & Organics-openings for Production, QA, CQA, IPQA, Engineering & Maintenance departments

Mangalam Drugs & Organics-openings

Mangalam Drugs and Organics Limited began its production of Active Pharmaceutical Ingredients (APIs) and Intermediates in VAPI, Gujarat, in 1977. The company operates a multi-product manufacturing facility across two sites and boasts an in-house Research & Development laboratory that is accredited by the Department of Scientific & Industrial Research, Government of India (DSIR).

There are immediate job openings available in Production, Quality Assurance, Engineering & Maintenance, Central Quality Assurance (CQA), and In-Process Quality Assurance (IPQA) at Mangalam Drugs and Organics Limited, Vapi, Units I and II.

Department: Production / Quality Assurance / CQA / IPQA/ Engineering & Maintenance
Position: Officer / Chemist / Executive
Qualification: B.Sc./ M.Sc./ B.Tech/ M.Tech
No of Vacancies: 13
Experience: 03-10 Years of relevant experience (API Only)

Work Location: Plot No.187, GIDC, Vapi – 396195 Dist- Valsad, Gujarat

How to Apply:

Interested candidates can share their CVs to hr1@mangalamdrugs.com &
mangalam12012@gmail.com
Contact Person: Ms. Krishna Patel

Note: Candidate should be from Vapi only and ready to relocate in Vapi

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

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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