Regulatory Affairs Associate - East Windsor, NJ

We are hiring Regulatory Affairs Associate I. · Please let me know if you are interested or anyone who might be interested. · Client: Major Cosmetics Client · Position: Regulatory Affairs Associate I · Duration: 11+ months · Location: Clark, · NJ 07066 ...

We are hiring Regulatory Affairs Associate I. · Please let me know if you are interested or anyone who might be interested. Review formulas for compliance with local regulations in US and Canada. · Reviewing artwork for US and Canada Compliance. · Notifying products in US and Can ...

This is a Regulatory Affairs Associate position that requires a Bachelors level degree in Science or related field and strong working knowledge of Chemistry. · ...

The Fountain Group is seeking a Regulatory Affairs Associate for a prominent client located in Clark NJ. · This position involves reviewing formulas for compliance with local regulations particularly US and Canada notifying products in US and Canada as needed maintaining KPIs as ...

The General Affairs Associate ensures smooth day-to-day office operations by managing facilities, procurement, assets, vendors and administrative services. · Oversee daily office operations to ensure a safe clean functional and welcoming work environment. · Coordinate facility se ...

The General Affairs Associate ensures smooth day-to-day office operations by managing facilities, procurement, assets, · vendors and administrative services. This role maintains a safe efficient and compliant workplace while coordinating internal needs · and external service prov ...

+The General Affairs Associate ensures smooth day-to-day office operations by managing facilities and administrative services. · ...

The General Affairs Associate ensures smooth day-to-day office operations by managing facilities, procurement, assets, vendors, and administrative services. · ...

The Regulatory Affairs Associate prepares annual reports with FDA within Annual report timelines and in accordance with regulatory guidelines. · ...

The General Affairs Associate ensures smooth day-to-day office operations by managing facilities, procurement, assets and administrative services. · ...

Ensures a controlled documentation system record retention and information services including electronic records retention processes in accordance with regulatory requirements. · Maintains the technical and non-technical documentation change system · Interprets and enforces all d ...

Ensures a controlled documentation system record retention and information services including electronic records retention processes in accordance with regulatory requirements. · ...

The Regulatory Operations Associate is responsible for publishing, QC, and transmittal of eCTD submissions, · as well as document formatting and report-level publishing. · ...

The Regulatory Operations Associate is responsible for publishing, QC, and transmittal of eCTD submissions, · e.g., using Acadia's eCTD publishing (IQVIA RIM Smart) and document management (Veeva Vault RIM), publish eCTD submissions and reports in alignment with health authority ...

The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. · We're changing lives for a living. Are you ready to make a difference? · The Associate Director, Medical Affairs Omnichannel Engage ...

We are dedicated to building extraordinary futures by developing antibody products that change lives and the future of cancer treatment.The Associate Director Global Medical Affairs Training is responsible for developing training curricula supporting Health Evidence Liaisons and ...

This position is for an Associate Director of Medical Affairs Omnichannel Engagement at Novo Nordisk. The role will support the execution and governance of medical omnichannel engagement strategy across specific therapeutic areas.The ideal candidate will have experience in projec ...

We're changing lives for a living. Are you ready to make a difference? · ...

The Associate Director, Global Medical Affairs Training is responsible for developing implementing continuously elevating Genmab training curricula supporting Health Evidence Outcomes Liaisons HEOLs cross-functional Medical Affairs partners. · Strategic Training Leadership Provid ...

The Associate Director will independently review, approve and monitor product advertising for assigned products to ensure compliance with US regulatory requirements. · ...