Demo S.A. Jobs in India

At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Post-Approval Manager to join our team. The candidate will be responsible for execution of post-marketing regulatory activities for MENA ...

Job Title: · Regulatory Affairs Post-Approval Manager · About Demo SA: · We are looking for talented professionals to join our team at one of the world's largest pharmaceutical manufacturers. · Main Responsibilities: · ...

At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Associate to join our team. The job responsibilities for this position includes post-marketing regulatory submissions for Europe and othe ...

At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Senior Associate to join our team. The job responsibilities for this position includes post-marketing regulatory submissions for Europe a ...

At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Senior Associate to join our team. The job responsibilities for this position includes post-marketing regulatory submissions for Europe a ...

Job Title: Regulatory Affairs Post-Approval Manager · This role involves managing variations, life-cycle management, and compliance for authorised products for sterile and non-sterile products globally. · Oversee planning, authoring coordination and submission of European variati ...

At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Associate to join our team. The job responsibilities for this position includes post-marketing regulatory submissions for Europe and othe ...

Regulatory Affairs Post-Approval Associate-Europe · This role involves post-marketing regulatory submissions for Europe and other global markets for sterile and non-sterile products. · Understanding of EU regulations including renewals and extensions · Collections preparation com ...

Job Summary · This role involves post-marketing regulatory submissions for Europe and other global markets for sterile, non-sterile, and oral solid/liquid products. · Main Responsibilities: · Understanding of Regulatory strategy and documentation requirements for EU variations in ...

At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Post-Approval Manager to join our team. The candidate will be responsible for managing variations, life-cycle management, and compliance ...

At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Post-Approval Manager to join our team. The candidate will be responsible for execution of post-marketing regulatory activities for MENA ...

At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Post-Approval Manager to join our team. The candidate will be responsible for managing variations, life-cycle management, and compliance ...

At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Post-Approval Manager to join our team. The candidate will be responsible for execution of post-marketing regulatory activities for MENA ...