Executive – Regulatory Affairs - chennai, India - TTK Healthcare

Regulatory Affairs and Scm

1 week ago

**Job Title**:Regulatory Affairs and SCM -Executive · **Location**:Chennai, India**Employment Type**:Permanent**About OMRON** · - Founded in 1933, OMRON has come a long way since and has evolved to become an organization committed to creating new social values. Today, In the APAC ...

Regulatory Affairs Officer

1 week ago

Explain regulations, policies, or procedures · - Maintain data in information systems or databases · - Ensure compliance with regulations · - Advise others on regulatory and compliance matters · - Evaluate applicable laws and regulations to determine impact on company activities ...

Executive - Regulatory Affairs (Plmds)

3 days ago

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds. · ClinChoice, is searching for an Executive - Regulatory Affairs (PLMDS) ...

Regulatory Affairs Executive

4 days ago

Job Summary · The Regulatory Affairs Specialist is responsible for ensuring compliance with all applicable · regulations governing the development, manufacturing, and distribution of the company's · products. This role involves collaborating with internal teams and regulatory age ...

HCL is Hiring Regulatory Affairs@Chennai

2 weeks ago

HCL Technologies is a next-generation global technology company that helps enterprises reimagine their businesses for the digital age. Our technology products and services are built on four decades of innovation, with a world-renowned management philosophy, a strong culture of in ...

Scientific Communication

21 hours ago

**Industry** · Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications · **Position** · Full Time, Permanent · **Division** · Pubrica Brand · **Reports to**: · Pubrica Business Head · **About Company** · Guires Group is a renowned glob ...

Associate I

3 days ago

Why Patients Need You · We're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attentio ...

Rapd Associate I

3 days ago

Contribute to the completion of project milestones and organize own work to meet project task deadlines. · - Ensure compliance of the team to the submission standards, procedures and policies framed by Global Regulatory Affairs. · - Responsible for the preparation and finalizatio ...

Associate Ii

1 week ago

Functions as Regulatory support for assigned projects and the life-cycle changes; works with Project Leads/Product Leads, cross-funcational teams, local and regional regulatory colleagues, external partners (in-licensed products) and Global Health Authorities (if required) to ind ...

Associate Ii

2 days ago

Manages day-to-day regulatory activities associated with assigned Renewals within agreed upon timelines under the guidance of Team Lead / designee. · Has fundamental knowledge of the principles and concepts of process been followed, the activities which includes but not limited t ...

Associate Ii, Cdm

1 week ago

Why Patients Need You · We're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attentio ...

Associate Ii

21 hours ago

Manages day-to-day regulatory activities associated with assigned Renewals within agreed upon timelines under the guidance of Team Lead / designee. · Has fundamental knowledge of the principles and concepts of process been followed, the activities which includes but not limited t ...

Rapd Associate I

1 week ago

Qualifications · Must-Have · - Bachelor's Degree · - Proven ability to manage complex regulatory or drug development issues · - Knowledge of the regulations and guidelines in the various markets · - Strong relationship with the local health agency and other relevant stakeholders ...

Rapd Associate I

1 week ago

Qualifications · Must-Have · - Bachelor's Degree · - Proven ability to manage complex regulatory or drug development issues · - Knowledge of the regulations and guidelines in the various markets · - Strong relationship with the local health agency and other relevant stakeholders ...

Associate I

1 week ago

Why Patients Need You · We're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attentio ...

Associate Ii

21 hours ago

Role Summary: · Functions as the CMC author & strategist for the Life Cycle Management (LCM) activities of assigned projects providing regulatory assessments and developing regulatory strategies for global markets including US/EU/APAC/LATAM & AfME regions; Accountable for assigne ...

Associate I

2 days ago

PROCESS IMPROVEMENT/ OPTIMIZATION INITIATIVES · - Represents India Strategy Organization for all GRA process improvement initiatives · - To work on deliverables related to optimization and efficiency in the processes and systems that are utilized within the India Strategy organiz ...

Associate Ii

17 minutes ago

Primarily Responsible for managing assigned regulatory projects/ CMC programs of moderate complexities, managing and ensuring daily delivery of regulatory and strategic activities, post · - approval regulatory submission activities for Brands in collaboration with Global Regulato ...

Associate Ii

2 days ago

Execution of CMC strategies for Pfizer Global Supply (PGS) initiated prioritized post approval changes globally in collaboration with the CMC GRS.- Global regulatory strategy development in collaboration with the CMC GRS.- Liaise with Pfizer Global Supply and other support functi ...

Associate Ii

3 days ago

Manages day-to-day regulatory activities associated with assigned LEC variations within agreed upon timelines. · - Evaluate change controls for completeness, accuracy and required supporting documents. Initiate change controls when needed. · - Performs Market Impact Assessment (M ...