- Walk-in Interview @ Amneal, Ahmedabad on 10th Dec’16 (Saturday)
There are multiple vacancies in PRODUCTION, QC, QA, ARD, F&D – OSD (oral solid dosage) unit for Amneal’s Ahmedabad Rajoda & SEZ Matoda Plant and for that company have arranged Walk-in Interview on coming SATURDAY, 10th Dec’16 at below address:
Walk-In Date: 10th Dec’16, Saturday
Timing: 9:00 AM to 2:00 PM
Amneal Pharmaceuticals Pvt. Ltd.
5th Floor, 508-514
Venus Atlantis Corporate Park,
Above Gwalia Sweets, near Prahladnagar Garden, Prahladnagar,
Landmark: Shell Petrol Pump
Please find the details of openings for our various departments:
1. Production – Solid Oral:
Qualification: ITI / D. Pharma / B. Pharma / M. Pharma
Exp: 0-5 Yrs
Job Title: Operator / Officer / Executives
Candidate must have exposure of Solid Oral Dosage Form. Please do not apply if you are from API / Injectable background. B. Pharma / M. Pharma fresher may also apply.Female are not allowed.
2. Quality Control-OSD
Qualification: B.Sc / M.Sc / B.Pharma
Exp: 0-4 Yrs
– Should have exposure of Solid Oral Dosage unit
– Please do not apply if having exposure of API / Injectable
– Should have exposure of various instruments like, HPLC, GC etc.
– USFDA exposure will be preferred.
3. Quality Assurance-OSD
Qualification: B. Pharma / M. Pharma
Exp: 1-8 Yrs
Job Title: Officer / Executives / Asst Manager
Desired: Candidate must have exposure of OSD unit. We have various opening in IPQA / Validation / QMS etc. Please do not apply if having API / Injectable background. FRESHER Are NOT allowed. USFDA exposure will be preferred
4. Analytical Research & Development (ARD/ADL- OSD):
Job Title: Officer/Sr. Officer/Executive/Sr. Executive
Qualification : M.Sc. (Analytical Chemistry)/ B.Pharm / M.Pharm
Experience : 02 to 08 years
Openings are for various groups in ARD like Exploratory, Method development, Raw Material Analysis, Routine & in process sample analysis, Stability group, Release group, Validation and Regulatory documentation group
5. Formulation & Development-OSD
Exp: 4+ Yrs
Job Title: Executive / Sr. Executive
Literature search on API, Formulation, BE study for new product development.
Understand different regulatory requirement for ANDA. Compile & maintained deficiency tracker. Procurement of API / excipients / Tooling for respective projects. Writing LNB of trial batches online and other relevant documents. Daily follow-up with interdepartmental (ARD, Production, QC, QA, Purchase etc)Execution of exhibit batches as per respective project time line. Providing documents required for licencing purpose (Form 29, Form 11).
– Please carry 02 copies of your CV along with CTC proof and 2 passport size photographs.
– You may refer this mail to your friends.
For any query you may write an E-mail to