RAKS PHARMA PVT. LTD.-HIRING for USFDA Approved API facility

RAKS PHARMA PVT. LTD.-HIRING for USFDA Approved API facility

RRaks Pharma
RAKS PHARMA PVT. LTD. Dahej, (Bharuch, Gujarat)
USFDA Approved API facility
(Group of Amneal Pharmaceuticals)
WE ARE HIRING
amneal
M/s. RAKS Pharma is fast growing API manufacturer in Dahej (Gujarat) India. Raks is an interesting blend of consistency in maintaining both quality standard and growth in terms of addition of new products to its existing list of API’s.
Officer/Sr. Officer – Production (API – Manufacturing)
Qualification: B.Sc / M.Sc. & B.E. Chemical / B.Tech. Chemical with good academic record. Experience: 1 to 6 years of experience from well-known Pharma / API Industries.
JOB PROFILE : Responsible for all API process operation/activities during the shift as per cGMP, To monitored process activity as per BMR/BPR/BCR during shift operation and record online and co- ordinate with all service department for fulfil the process requirement, Maintain safety norms in plant during process operation.
Venue for the Interview
Raks Pharma Pvt. Ltd., Plot No. Z/111/A, Dahej SEZ-II, Ta. Vagara, Dist. Bharuch -392130. (Gujarat)
Person who have faced regulatory audits like USFDA would be given preference.
Interested candidates can send their updated CV with the code (RAKS DAHEJ PROD) in the subject line to below mail id.
harshad.d.bhavsar@amneal.com
Note: E-mail without code in subject line will not be considered for further processing.

Job Category: pharma
Job Type: Full Time
Job Location: Bharuch -392130. (Gujarat

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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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