Compliance & Regulatory Affairs Manager - Pitampura, Delhi, Delhi

About the role We are seeking a dynamic and strategic Corporate Affairs Manager to oversee and manage the company's interactions with internal and external stakeholders including regulatory bodies government agencies industry groups media and the public This role is critical in s ...

Zoot Systems is a New Delhi, India based company. For years, it has been our continuous endeavours to understand Client quality-conscious discerning business needs and to successfully meet those. We specialize in the creation of high-quality I.T./Non-I.T. based HR Solutions, Recr ...

Plans and executes events from concept to completion managing budgets vendors logistics and client communication. · ...

This role involves developing and implementing effective government affairs strategies to promote the company's interests in the power industry. · ...

We are looking for a dynamic professional with proven expertise in corporate communication and government liaising. · Build and maintain relationships with government authorities. · Facilitate teams in pursuing new business opportunities. · ...

Seeking Compliance & Regulatory Affairs Manager (5+ yrs exp) to ensure global/domestic compliance and manage submissions labeling audits. · ...

The Public Affairs Manager will drive stakeholder centricity across India by establishing managing customer and government relationships gathering market intelligence advising the CCO on commercial opportunities laying groundwork for developing new customers. · Master`s level edu ...

Thepharmadaily LLP is looking for Regulatory Affairs Executive/ Manager to join our dynamic team and embark on a rewarding career journey · Regulatory Compliance: Monitor changes in regulations and legislation that pertain to the organization's industry and products to ensure com ...

Seeking Compliance & Regulatory Affairs Manager (5+ yrs exp) at Wonder Products. · ...

Driving policy advocacy, regulatory engagement and government relations to support business objectives in the medical devices sector. · Tracking policy developments, representing the company at industry forums and engaging with government stakeholders. · ...

Should have minimum 14+ years of relevant experience in Corporate Affairs and Regulatory matters · Roles and Responsibilites: · Play a key role in designing and implementing a structured liaisoning framework, and oversee the development, execution, and assessment of activities re ...

This is a unique opportunity to make a real impact at the intersection of entertainment policy and global affairs. · ...

The Public Affairs Manager will drive stakeholder centricity across India by establishing and managing customer and government relationships. · ...

Should have minimum 14+ years of relevant experience in Corporate Affairs and Regulatory matters · Play a pivotal role in setting up structured liaising plan, develop, administer, and evaluate activities and operations related to the Governmental affairs and Ministries · Represen ...

· Job Description: · Oversee and manage commercial agreements and legal compliance. · Handle contract negotiations and mitigate legal and commercial risks. · Ensure adherence to regulatory requirements and industry standards. · Coordinate with internal departments to ensure cont ...

The Manager - Regulatory Affairs will be responsible for overseeing US regulatory operations and ensuring compliance for product portfolios in the US market. · ...

The Manager - Regulatory Affairs will be responsible for overseeing US regulatory operations. · ...

The Regulatory Affairs team brings new medical advancements to the world by facilitating communications and procedures that allow swift compliance partnering with external regulatory agencies. · We are on the leading-edge of healthcare breakthroughs that help provide reliable and ...

The Manager - Regulatory Affairs will be responsible for overseeing US regulatory operations, · 12-15 years of experience in US Regulatory AffairsProven expertise in USFDA regulatory strategy and submissions ...

Must have knowledge of CTD & country specific dossiers compilation site master files SMF & stability study reports regulatory submissions prepare and submit regulatory documentation including applications amendments and notifications to health authorities ensure compliance with r ...