...regulatory authorities) on defined matters.
·
Face external audits / inspection, coordinate and communicate with external auditors / inspectors for compliance.
Qualifications
Expertise in regulatory compliance ...
Job Overview
Full-time position based in Gurgaon, responsible for leading the global regulatory activities of our agrochemical products. The ideal candidate will have extensive experience in regulatory affairs and a strong understanding of glob...
...dossiers for different dosage forms as per products for different countries.
Coordination for sample and test reports.
Please send your updated resume with current salary, expected salary and Notice period to [HIDDEN TEXT].
be...
...of Modules-I as per regulatory requirement.
Note: The candidate can work individually.
Regulatary Affairs,dossiers,regulatory documents
Designation: Assistant Manager/Sr..Regulatory Affairs Off...
...labeling materials with the Generics Law and other relevant laws.
c) Ensure regulatory support to GMP inspections if required
d)... ...relevant regulations (e.g. FDA
EMA).
Profici...
My client are seeking a highly skilled Regulatory Affairs Team Lead to join their dynamic team in India. The ideal candidate will have extensive experience in regulatory affairs, particularly in handling DCP submissions, and...
Required Finance SOP Compliance Specialist
Location: Surat Gujarat India
Industry Pharma Industry
Must have 25 years in Finance SOP Compliance preferably from a Pharma background
We are currently seeking a highly skilled and motivated Fi...
Job Title:
Regulatory Specialist
Company:
Concept Medical
Location:
Surat, Gujarat
Job Type:
Full-Time
About Us:
Concept Medical is at the forefront of developing and manufacturing innovative medic...
...affairs activities to assist in regulatory submission, annual reports, registrations and listings. Assure compliance with applicable medical device regulations per jurisdiction, guidance and standards. Assist in cre...
...regulatory requirements at GPC Medical.
Roles and Responsibilities
· Prepare and update technical documentations as per EU MDR and 510 (k) regulatory requirements as required.
· Prepare and update risk management...
New Delhi
GPC Medical Ltd.
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