HETERO Biopharma - Urgent Openings for Production & Regulatory Affairs - Apply Now
Hiring for Production Compliance Position
Dear All,
Greetings from Hetero Biopharma
Hiring for Production Compliance position with Formulation (OSD) Experience only.
Department: Production Compliance
Designation: Jr. Officer/ Officer
Experience: 1 to 3 yrs
Job Location: Jeedimetla (Hyderabad)
Qualification: B.Pharmacy/M.Pharmacy/M.Sc
Interested candidates forward their resumes to Bhagyalakshmi.bu@heterodrugs.com
Opening For Regulatory Affairs Position
Dear All,
Greeting from Hetero Biopharma.
We have opening for Regulatory Affairs AM/DM Position
Department: Regulatory Affairs
Designation: Sr. Exe / Asst. Mgr
Experience: 4 Yrs to 9 Yrs
Job Location: Jadcherla (Telangana)
1. To verify the country specific guidelines, evaluate & submit the dossiers as per the client/MOH requirements.
2. To prepare the dossiers (eCTD, CTD & country specific format) that review, organization for AFRICAN, CIS, LATAM and MENA region countries.
3. Receipt and submission of responses to the queries of dossier of data packages submitted to AFRICAN, CIS, LATAM and MENA countries.
4. To co-ordinate with cross functional teams to initiate the new studies for suffice the query response & dossier requirement towards country specific requirements for product registration.
5. To prepare & submission of post approval changes (PAC) in accordance with country specific variation guidelines & get the approvals.
6. Keeping abreast with updating of country specific regulations and guidance.
Interested Candidates share profile to edukondalu.m@heterodrugs.com
Greeting from Hetero Biopharma.
We have opening for Regulatory Affairs AM/DM Position
Department: Regulatory Affairs
Designation: Sr. Exe / Asst. Mgr
Experience: 4 Yrs to 9 Yrs
Job Location: Jadcherla (Telangana)
1. To verify the country specific guidelines, evaluate & submit the dossiers as per the client/MOH requirements.
2. To prepare the dossiers (eCTD, CTD & country specific format) that review, organization for AFRICAN, CIS, LATAM and MENA region countries.
3. Receipt and submission of responses to the queries of dossier of data packages submitted to AFRICAN, CIS, LATAM and MENA countries.
4. To co-ordinate with cross functional teams to initiate the new studies for suffice the query response & dossier requirement towards country specific requirements for product registration.
5. To prepare & submission of post approval changes (PAC) in accordance with country specific variation guidelines & get the approvals.
6. Keeping abreast with updating of country specific regulations and guidance.
Interested Candidates share profile to edukondalu.m@heterodrugs.com
FOR MORE JOB UPDATES
No comments:
Post a Comment