...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...
..., working standards, document data, license related documents.
~ Should have knowledge with regard to checking of samples.
~ Courier of documents and samples to the respective customer.
~ Maintaining sta...
...As a Senior Quality Engineer you will be a key member of the Medtronic Post Market Quality Engineering team responsible for maintaining highest standards of product reliability and patient well-being through gather ...
...regulatory submissions and activities for products throughout the life-cycle of a product in compliance with Health Canada regulatory requirements... ...to junior staff in the creation of sub...
...Respiratory Care is a medical device company with a product portfolio of respiratory solutions focused on airway clearance and ventilation therapies. Our mission is to advance the healthcare industry by developing i...
Position name – Global Quality Head (Pharmaceutical Manufacturing)
Years of experience – 16-27 years
Industry - Pharmaceutical Manufacturing
Job Location - Maharashtra
Client - leading pharmaceutical manufacturing
Responsibilities:
- Drive an...
...Working location shall be around 20 Km from Vadodara and company transport will be available.
Regulatory Affairs,Regulatory Compliance,dossier registration,CTD,ACTD
Designation: Assistant Regulatory ...
...following key services to GRA colleagues in support of achieving GRA business objectives:
Responsibilities of this role are:
Supervise, mentor and support the work of junior colleagues.
Supports in resource...
Bangalore
GSK India
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