Gufic Biosciences-Interview For Production/ QA/ Engineering/ QC Chemical & Microbiology on 18 Feb 2024

Gufic Biosciences-Interview For Production/ QA/ Engineering/ QC Chemical & Microbiology on 18 Feb 2024

One of the world’s largest lyophilized injectable plant : Indore

1) Department: Production

Education: Diploma/ ITI/ B.Pharm

Experience: 1-8 years

Designation: Jr. Technician/ Technician/ Officer

Vacancies for: Vial Washing, Autoclave, GMP Washer, Filling & Sealing, Vial Collection, Terminal Sterilizer, Visual Inspection, Xray, Packing, Blister, Cartonator

2) Department: Quality Assurance

Education: B.Pharm/ M.Pharm/ M.Sc

Experience: 1-7 years

Designation: Officer/ Sr. Officer/ Executive/ Assistant Manager/ Manager

Vacancies for: Validation & Qualification, Lab QA, IPQA, QMS

3) Department: Engineering

Education: B.E/ B.Tech/ Diploma/ ITI

Experience: 1-7 years

Designation: Operators/ Officer/ Executive

Vacancies for: Engineer- Documentation/ instrumentation / Machanical Operators for HVAC, Lyophilizer, Fitter, Refrigeration

4) Department: QC Chemical & Microbiology

Education: M.Sc, B.Sc, B.Pharm, M.Pharm

Experience: 1-5 Years

Designation: Officer/ Sr. Officer

Vacancies for: AMV, PV, RM/PM/FP, Stability MLT, BET, Assay, EM, Media Preparation, Culture Identification

Eligibility – Prior working experience in Injectable formulation

Date: Sunday, 18/02/2024

Time: 10:00 am to 05:00 pm

 Venue: – Hotel Royal Shelter Gunjan Chokdi, National Highway No. 8, Vapi, Gujarat 396191

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

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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