Job Description
- Preparation and submission of DMF (eCTD) for Certificate of suitability (CoS) & regulatory guidelines for Drug Substances in US, European market
- Preparation and compilation of reports,amendments etc. for USDMF
- Review of BPRs,Specifications
- Preparation and compilation of reports,amendments etc. for USDMF
- Review of BPRs,Specifications
Salary:
INR 2,00,000 - 5,00,000 P.A. Depends on candidates experience & skills.
Industry:
Pharma, Biotechnology, Clinical Research
Functional Area:
Legal
Role Category:
Drug Regulatory Affairs/Documentation
Role:
Regulatory Affairs Manager
Keyskills:
ra, regulatory affairs officer, regulatory affairs, affairs regulatory,cos, ra officer, ra executive, bulk drug, api, Regulatory, DMF, eCTD, BPRs, USDMF, tarapur, boisar, pharma, pharmaceutical, palghar, dahanu, vasai, vapi
Desired Candidate Profile
Education:
(UG - B.Sc) OR (PG - M.Sc)
- Qualification :- B.sc / M.sc
- Male Candidates with minimum 2 year experience can apply
- Should have good Interpersonal skills with excellent communications skills.
- Computer Skills MS-Office / MS-Word
- Male Candidates with minimum 2 year experience can apply
- Should have good Interpersonal skills with excellent communications skills.
- Computer Skills MS-Office / MS-Word
Company Profile
For a Pharma Ltd Co.(An MNC GROUP) C/o Shree Ganesh Enterprises.
- A Pharma Ltd Co (An Mnc Group) having its plant at Tarapur- Boisar in Thane(District)(Bulk Drugs API Manufacturing)
- Client of Shree Ganesh Enterprises (Placement Services)
Contact Details
Executive Name:
Mr. Kamlesh
Contact Company:
Shree Ganesh Enterprises
Email Address:
Telephone:
9028000158,9049355064
by For a Pharma Ltd Co.(An MNC GROUP) C/o Shree Ganesh Enterprises. in Tarapur, Thane, Mumbai
Experience: 2 to 7 yrs. | Salary: INR 2,00,000 - 5,00,000 P.A
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