Virology Regulatory Specialist, Associate Director

**Job Description**Gilead Sciences, Inc. is a leading biopharmaceutical company that seeks an experienced Regulatory Affairs professional to join its team as an Associate Director, Global TA Regulatory Liaisons, Virology. This role will oversee the preparation and maintenance of regulatory submissions, labeling, and packaging for assigned products or...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Director to lead our Global Therapeutic Area (TA) Regulatory Affairs team in Virology. As a key member of our team, you will be responsible for defining the regulatory strategy, plans, and objectives for assigned products or projects. You will also oversee the preparation and maintenance of...

**Job Summary**Gilead Sciences, Inc. is a biopharmaceutical company that develops life-changing scientific innovations. We are seeking an experienced Regulatory Affairs professional to join our team as an Associate Director, Global TA Regulatory Liaisons, Virology.This role requires a deep understanding of European Medicines Agency (EMA) regulations and...

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Proclinical are recruiting for a Regulatory Affairs Associate to join a pharmaceutical organisation. This role is on a contract basis and is either located in Uxbridge or Cambridge. **Key Skills and Requirements**: - Familiarity in an administrative field within a corporate or similar setting preferably within a healthcare sector. - Educated to a degree...

Transforming Lives through Regulatory ExcellenceBristol Myers Squibb is a company that pushes the boundaries of what's possible in the world of pharmaceuticals. As an Associate Director, Global Regulatory Sciences, Precision Medicine, you'll be at the forefront of this innovation, driving regulatory strategies that bring life-changing treatments to patients...

We are seeking a talented Regulatory Affairs Specialist to join our dynamic team at BTA. As the CMC Regulatory Manager, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products.Key Responsibilities:Develop submission strategies and...

Job DescriptionWe are seeking a highly skilled Director, Regulatory to join our team at Gilead Sciences. As a key member of our quality assurance department, you will be responsible for leading the development and implementation of procedures and templates to assist in the evaluation and improvement of our auditing process. This will include developing...

Lifelancer offers a unique opportunity for a talented professional to join our team as a Global Regulatory Sciences Director. This role is an excellent fit for individuals who are passionate about transforming patients' lives through science.As a Global Regulatory Sciences Director at Lifelancer, you will be responsible for leading the development of...

The Director of Regulatory Affairs will provide strategic leadership on global regulatory activities for assigned products. Responsibilities will focus on Clinical Regulatory filings and provide regulatory guidance on project teams in this area. We are a hands-on culture, so responsibilities will include support to some clinical study activities.Key...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Senior Regulatory Affairs Associate / Regulatory Affairs Manager EU contract jobYour new company This global biopharmaceutical company is looking for an experienced Regulatory Affairs professional to join them on a contract basis, 12 month, hybrid contract job with scope for extensionYour new role As Senior Regulatory Affair Associate / Regulatory Affairs...

Career Category Regulatory **Job Description**: - Job Description: - Amgen is a leading human therapeutics company in the biotechnology industry. For more than 40 years, the company has tapped the power of scientific discovery and innovation to advance the practice of medicine. As a Fortune 500 company serving millions of patients. Amgen continues to be...

The Director- QA Compliance, will report to the Executive Director of Supplier Management and Auditing. This key position will be the acting Global Process Owner for External Audits and conduct GMP audits of Gilead's global suppliers with a primary focus on external biologics manufacturing, contract packaging and contract testing labs.Responsibilities:Lead...

About the Role:The Global Regulatory CMC Director will be responsible for developing and implementing global regulatory strategies for cell therapy products, ensuring compliance with current regulations and guidelines.Key Responsibilities:Represent regulatory CMC on and/or lead matrix teams for cell therapy pipeline products and/or commercial products...

Lifelancer is seeking a highly qualified Principal Regulatory Affairs Consultant to join our team. As an Associate Director level professional, you will be responsible for providing expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule development.This role offers a unique opportunity to showcase your technical skills, specialist...

Regulatory Affairs Senior Associate RoleWe are seeking a highly skilled Regulatory Affairs Senior Associate to join our team at Regeneron Pharmaceuticals Inc.About the RoleThis is an exciting opportunity for a talented individual with a passion for regulatory affairs to support our CMC Regulatory submissions. As a key member of our team, you will play a...

Transform Patients' Lives through ScienceBristol Myers Squibb is a leader in the pharmaceutical industry, dedicated to transforming patients' lives through science. As an Associate Director of Scientific Writing, you will play a crucial role in ensuring the accuracy and quality of regulatory documents.About the RoleWe are seeking an experienced professional...

About the Role:Gilead Sciences, Inc. is a leader in the development of innovative therapies that address some of the world's most pressing health challenges. We are seeking an experienced Associate Director to join our dynamic Medical Writing team.Key Responsibilities:Develop and author high-quality regulatory documents, including clinical study reports,...