Regulatory Submission Lead - Mexico City

We are seeking a Regulatory Submission Lead to support the lifecycle management of pharmaceutical products in Mexico City. · Candidate must have strong understanding of regulatory submission requirements and lifecycle management processes. · ...

Are you ready to make a meaningful impact in a dynamic regulatory role? As a Submission Lead in Submission Delivery Excellence, Lifecycle Management, you will play a key role in ensuring the timely and high-quality delivery of regulatory submissions. · ...

We are seeking professionals with the following required skills and qualifications to help us achieve our goals:Bachelor's degree in pharmacy, chemistry, biotechnology or a related field. · Strong understanding of regulatory submission requirements and lifecycle management proces ...

We have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. · ...

This role will provide YOU the opportunity to lead key activities to progress YOUR career. · Own end‑to‑end delivery of assigned complex lifecycle regulatory submissions (e.g., variations, PBRERs, renewals, site registrations/renewals, tenders, etc.), ensuring they meet agency re ...

We are looking for a Legal Directory Specialist (LDS) to lead the end-to-end management of legal directories and rankings · (Chambers & Partners, The Legal 500, IFLR, Leaders League, among others). This role is pivotal to strengthening the visibility and reputation of firms and l ...

+Join Amgen's Mission of Serving Patients to help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. · Master's degree in health sciences or related field · Bachelor's degr ...

Job summary · We are seeking a Senior Translations Project Manager to coordinate and manage Regulatory Submissions translation/localization projects from receipt to completion. · ...

Syneo Health is looking for Senior Regulatory Consultants who will contribute to their project teams by providing technical expertise in proposals, assisting with Business Development initiatives, understanding project budgets, scope of projects allocated hours tracking complianc ...

We are looking for a Start-Up Specialist to join our team and make a difference in the execution of study start-up activities. · ...

Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access – Providing high quality trusted medicines regardless of geography or circumstance; Leadership – Advancing sustainable operations and innovative solutions to improve patient health; a ...

Astellas' Global Capability Centres – Overview Astellas' Global Capability Centres are strategically located sites that give Astellas the ability to access talent across various functions in the value chain and to co-locate core capabilities that are currently dispersed. Our thre ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · ...

Regulatory Affairs Director in Mexico for a leading global pharmaceutical company. Opportunity to shape regulatory operations from the ground up. · ...

Job summary · Sr. Técnico Regulatorio - Solo México D.F. · Proactivo identificar y mitigar riesgos a través del sistema CTIS relacionados con documentación y subir datos en línea · ...

This job is with Johnson & Johnson, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. · We are searching for the best talent for Regulatory Affairs Head to be in our Mexico City office. · ...

We're looking for an inspiring Clinical Operations Manager to lead a team of 20 professionals across clinical operations — ensuring excellence in performance, quality, compliance, and delivery. · In addition to core Clinical Operations leadership, this role plays a key strategic ...

As a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you will be central to the successful delivery of complex global oncology clinical trials (Phases I–III) for some of the world's most renowned and innovative pharmaceutical ...

As Regulatory Technician you will work with the Clinical Trials Information System (CTIS) providing support for submissions documents by performing necessary tasks including assembly dispatch among others coordinating resources for submissionsProactively identify mitigate risks t ...

+Job summary · Make a real difference in the lives of patients.+Monitor regulatory intelligence with stakeholders. · Prepare submission documents for Health Authorities. · ...