Job Title / Designation
Regulatory Affairs (RA)
Job Description / Responsibilities
1) Responsible for obtaining approval for new pharmaceutica ...
Job Title / Designation
Regulatory Affairs (RA)
Job Description / Responsibilities
1) Responsible for obtaining approval for new pharmaceutica ...
2) Updating legal or regulatory knowledge
2)Learn the regulations that apply to the products in said subfield
3)Compilation of Dossier as per Country requirement i.e. CTD,ACTD or Country Specific .
4)Co-ordination with F & D, BD, QA,QC, Purchase as per relevant Department for Document requirement
5)Handling of Query as per Ministry of Country
6) Reviewing documents required for submissions to ensure they are appropriate for submissions.
7) Maintained RA product files to support compliance with regulatory requirements.
8) Provided regulatory support for currently marketed products as necessary.
9) Maintains status registration of each country per distributor or representative agent of each product line.
10) Variation filing for product as per country guideline
11) Reviewing & checking of Artwork as per country requirement.
12)Responsible for the interpretation, direction, determination, and reporting of regulatory agency requirements.
13) FDA Application : Product Permission, Free Sale Certificate, Certificate of Pharmaceutical Product, Test License, Renewal Manufacturing License for Own & Loan.
Minimum Skill Required
About company (Industry, Size, Products/Services, Standing in India/World etc.)
Pharmaceutical Manufacturer and exporter of formulations (tablets/capsules), Supplements, and semi finished dosages (DC Granules).Been in business for 30 years with reputation for high quality and wide range of medicines across therapeutic categories.
Desired profile of the candidate
Candidate preferred be from Pharma / CDMO / EOU pharma companies
Background.
Learning Attitude.
Experience
1 – 10 years
Salary (Min & Max)
As per Candidate & Exp
Qualification
B.Pharm/M.Pharm
Job Location
Hyderabad, India
Interested candidayes can share CVs at jhelam.s@randstad.in
Job Title / Designation
Regulatory Affairs (RA)
Job Description / Responsibilities
1) Responsible for obtaining approval for new pharmaceutical product
2) Updating legal or regulatory knowledge
2)Learn the regulations that apply to the products in said subfield
3)Compilation of Dossier as per Country requirement i.e. CTD,ACTD or Country Specific .
4)Co-ordination with F & D, BD, QA,QC, Purchase as per relevant Department for Document requirement
5)Handling of Query as per Ministry of Country
6) Reviewing documents required for submissions to ensure they are appropriate for submissions.
7) Maintained RA product files to support compliance with regulatory requirements.
8) Provided regulatory support for currently marketed products as necessary.
9) Maintains status registration of each country per distributor or representative agent of each product line.
10) Variation filing for product as per country guideline
...
11) Reviewing & checking of Artwork as per country requirement.
12)Responsible for the interpretation, direction, determination, and reporting of regulatory agency requirements.
13) FDA Application : Product Permission, Free Sale Certificate, Certificate of Pharmaceutical Product, Test License, Renewal Manufacturing License for Own & Loan.
Minimum Skill Required
About company (Industry, Size, Products/Services, Standing in India/World etc.)
Pharmaceutical Manufacturer and exporter of formulations (tablets/capsules), Supplements, and semi finished dosages (DC Granules).Been in business for 30 years with reputation for high quality and wide range of medicines across therapeutic categories.
Desired profile of the candidate
Candidate preferred be from Pharma / CDMO / EOU pharma companies
Background.
Learning Attitude.
Experience
1 – 10 years
Salary (Min & Max)
As per Candidate & Exp
Qualification
B.Pharm/M.Pharm
Job Location
Hyderabad, India
Interested candidayes can share CVs at jhelam.s@randstad.in
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