Biozenta Lifescience – Urgent Openings for QC / Regulatory Affairs / Business Development / Accounts / Graphic Designer / DGFT / Calling Persons

Biozenta Lifescience – Urgent Openings for QC / Regulatory Affairs / Business Development / Accounts / Graphic Designer / DGFT / Calling Persons

We are Hiring For Biozenta Lifescience Pvt. Ltd.
New Openings @ Mohali (Punjab) location, local persons prefer…………….
suitable candidates can share their CV on 
hr@biozenta.com
coordinator1@biozenta.com, 7807792500, 9805808847( Calling time 9:00am To 6:00pm)

Share this post to your suitable connections so that we can find best Candidates
1)Business Development :- 2-6 years of experience in pharma line and candidate having knowledge Latin America, Asian, African market  (02 vacant )
ii) Institutional market, Domestic, hospital market and candidate also having great experience in Oncology field as well .
Location :- Mohali .
2) Regulatory affairs :– 2-5 years of experience in pharma line (05 vacant post )
Location :- Mohali and Una
3) Calling Persons :- 2+ years of experience in pharma line, FLUENT in English ( 02 vacant post )
4) Accounts :- 09+ years CA level person having pharma line experience (01 vacant post )
5) Graphic designer :-2+ years of experience (01 vacant post ) for una location
6) DGFT :- 2– 05 Years of experience who will be able to handle independent to handle all compliances in Pharma line (01 vacant post )
07) Quality Control :- GC person required candidate having 3-05 years of rich exeprince .
With Regards
HR Department

Job Category: pharma
Job Type: Full Time
Job Location: Mohali (Punjab)

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About Abha Maurya

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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