Acme Generics – Mega Walk-In Interview for Freshers in QA / QC / Production / Packing / Engineering / Warehouse / Microbiology / Regulatory Affairs on 23rd & 24th Sep’ 2023

Acme Generics – Mega Walk-In Interview for Freshers in QA / QC / Production / Packing / Engineering / Warehouse / Microbiology / Regulatory Affairs on 23rd & 24th Sep’ 2023

 

Acme Generics Pvt. Ltd established in 2004, in Nalagarh, Distt. Solan (Himachal Pradesh) is engaged in the manufacturing of research based Pharmaceutical products and has emerged as a leading third party manufacturer in the Domestic and International markets. we are looking young and dynamic personal with proven track record, who have exposure to advance / regulatory market operation (USFDA, Europe) for OSD & Injectable Formulation @ Baddi & Mohali

Excellent opportunity for freshers to join us at our Sterile and OSD Formulation Manufacturing Facilities at Baddi and Head Office at Mohali.
QUALIFICATION:
  • B. Pharma/M. Pharma/D. Pharma, B.Sc/M.Sc.(Chemistry, Microbiology. Biotechnology). ITI, B.Tech.
DEPARTMENTS:
  • Production, Packing, Warehouse, Engineering, Regulatory Affairs, Quality Assurance, Quality Control & Microbiology
Job Description: 
  • Department: QA / QC / Production / Packing / Engineering / Warehouse / Microbiology / Regulatory Affairs
  • Designation: Trainee
  • Qualification: B.Pharm, M.Pharm, M.Sc, B.Sc, D.Pharm, B.Tech, ITI
  • Experience: Freshers
  • Job Location: Baddi & Mohali
Job Category: pharma
Job Type: Full Time
Job Location: Baddi & Mohali

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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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