Sidmak-URGENT REQUIREMENTS FOR DEHRADUN PLANT

Sidmak-URGENT REQUIREMENTS FOR DEHRADUN PLANT

 

Sidmak is a leading integrated USFDA Approved Plant
A manufacturing facility having approval from USFDA Authorities, We develop and manufacture Tablet, Capsule & Transdermal Patches using its extensive experience and various technology platforms developed over last 35 years.

URGENT REQUIREMENTS FOR DEHRADUN PLANT B.Sc./B. Pharma./ M.Sc./ M. Pharm.
With 01-05 yrs. of relevant experience, USFDA/MHRA/WHO/Regulatory Exposure is must.
1.) PRODUCTION- (Chemist/officer) 01 to 02 Years: Experience in primary and secondary Packing.

2.) QUALITY ASSURANCE- (Sr. Officer/Executive):01 To 05 year: Experience in QMS.

3.) QUALITY ASSURANCE- (Officer/Sr. Officer):01 to 02 year: Experience in IPQA Section.
Interested Candidates can send CV on below mentioned Mail IDs:- monikachauhan@sidmak.com. career@sidmak.com
You can also contact our P&A department on-
Mobile -7505179663, 9193763000 Office-01352698509
Our Address-:
Sidmak Laboratories(India) Pvt. Ltd.
TRAV
Plot No.20, Pharmacity, Selaqui Industrial Area, Selaqui, Dehradun, (Uttarakhand)-248197 Website-:www.sidmak.com

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

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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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