BAL PHARMA LIMITED Walk-in-Interview for QA, QC, Production, Maintenance, Fitter & EHS from 10 to 13 Jan 2024

BAL PHARMA LIMITED Walk-in-Interview for QA, QC, Production, Maintenance, Fitter & EHS from 10 to 13 Jan 2024

 

BAL PHARMA LIMITED Walk-in-Interview for QA, QC, Production, Maintenance, Fitter & EHS from 10.01.2024 to 13.01.2024

A Leading Pharmaceutical company invites potential talent to be part of it’s growing journey.

WE’RE HIRING

Walk-in-Interview from 10.01.2024 to 13.01.2024 01:00 pm to 05:00 pm

For European Approved API Plant

Production-Shift Incharge

B.Sc/ M.Sc. Chemistry/ B.Tech Chemical with minimum 5-10 years experience of APL

Maintenance-Jr. Officer/ Officer

B.Tech. Mechanical with 2 to 10 years experience of API/ Chemical

Fitter-ITI in Fitter with 2 to 10 years experience of API/ Chemical

Quality Assurance-Officer/ Sr. Officer

M.Sc./ B.Pharma with 2 to 10 years experience of API.

Quality Assurance-Jr. Officer

M.Sc/ B.Pharma Fresher can also apply.

Quality Control-Sr. Officer/Executive

M.Sc./ B.Pharma with 2-10 years experiance of API

Quality Control-Officer

M.Sc./ B.Pharma with 2-10 years experiance of API.

EHS- Sr. Officer

Diploma in Health & Safety. with 5-10 years experiance of API

Meet us @ –
Golden Drugs Pvt. Ltd (A subsidiary of BAL Pharma Ltd.) C-155, Mewar Industrial, Area, Madri, Udaipur-313003, Rajasthan

Ph: 0294-2490411-9928704407 E-mail unit6admin@goldendrugs in

Please carry your updated resume along with last 3 months payslips & aadhar card.

 

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

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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