Lead Counsel Regulatory, Safety

**Position Purpose**: The Dir., Sr. Global Regulatory Lead, Hematology TA, is a member of a GRA GPS Therapeutic Area and contributes to the vision and goals for Global Regulatory Affairs (GRA) as: - ** GRA** Representatives** **on Product/Project Strategy Teams (PSTs), key Delivery Teams (e.g., Clinical Development Teams [CDTs], Safety Management Teams...

In order to complete our team of team of experts in Global Regulatory we our looking for a Global Regulatory Study Lead. In this challenging and important role you will be expected to: 1) Lead CTA activities for global clinical trials during the entire study lifecycle - Develop the CTA submission strategy for clinical trials - Act as an accountable interface...

**Responsibilities**: - Plan, direct, and monitor regulatory affairs activities so the organization has the permits, licenses, certificates, authorizations, and other approvals needed to conduct current and future business activities; and produce, sell, and distribute its goods and services. - Support development of consistent roles and work processes. -...

The Regional Regulatory Representative is responsible for all regional regulatory strategic and operational tasks for a range of products in the assigned Therapeutic Areas (TA) and Intercontinental (ICO) Region (Latin America, Eastern Europe (non-EU), Middle East and Africa). In consultation with the Therapeutic Area Lead, Regional Regulatory Lead...

CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, haematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Global Regulatory Affairs...

**Our client is a distinguished Energy trading company with a global presence.** **Location - Switzerland, France & Singapore** As the Legal Counsel, you will be responsible for leading and managing the company's legal affairs worldwide. This position will be responsible for overseeing and managing all legal matters, including contracts, litigation,...

Responsibilities: The Pharmacovigilance & Regulatory Quality Assurance (PVRQA) Lead / PV Auditor is responsible for leading and coordinating the Global PVRQA activities in the respective region (Americas, Asia-Pacific (APAC), European Economic Area (EEA), ECI) under the general direction of the PVRQA Regional Head, to ensure that CSL's (CSL Behring / CSL...

Responsibilities: The Pharmacovigilance & Regulatory Quality Assurance (PVRQA) Lead / PV Auditor is responsible for leading and coordinating the Global PVRQA activities in the respective region (Americas, Asia-Pacific (APAC), European Economic Area (EEA), ECI) under the general direction of the PVRQA Regional Head, to ensure that CSL's (CSL Behring / CSL...

The Opportunity We are looking for a Regulatory Quality Assurance (RQA) Lead to join the global Quality team on an ongoing basis. Based anywhere in the Asia Pacific region and working globally, you will provide oversight for the development and maintenance of sustainable and scalable, globally aligned quality processes across Global Regulatory...

**The Life Science Career Network** **Regional/Local Regulatory Head - 5373 LBD** Our client, a large pharmaceutical organization, is looking for a **Regional/Local Regulatory Head** for a** 12-month contract (with possibility of extension) in Bern**. **Responsibilities**: - Support GRA Region Intercontinental team members to obtain and maintain...

The Associate Director, Global Critical Safety Systems is accountable for development, deployment and governance of core technical environment, health and safety (EHS) processes and standards across all CSL/Seqirus units. You will help ensure global program understanding, and implementation. You will collaborate as part of the Global EHS team, reporting into...

Swissmedic ist die Schweizerische Überwachungsbehörde für Arzneimittel und Medizinprodukte. Sie gewährleistet, dass nur qualitativ einwandfreie, sichere und wirksame Heilmittel in der Schweiz in Verkehr gebracht werden. Die **Abteilung Arzneimittelsicherheit** begutachtet unerwünschte Arzneimittelwirkungen, klärt vermutete Risiken ab und setzt...

Beschreibung: We make it GmbH is a nationally active company in Switzerland with a high level of expertise in the field of personnel services thanks to many years of successful experience. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We at it GmbH set the highest...

**CMC Lead - Plasma Product Development - 5378 URA** Our client is a specialist biotherapeutics manufacturer with over a century of experience treating various diseases worldwide. They are committed to patients with coagulation disorders, immunological diseases, enzyme deficiency diseases and other rare diseases. This senior leadership role will be...

We make it GmbH is a nationally active company in Switzerland with a high level of expertise in the field of personnel services thanks to many years of successful experience. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We at it GmbH set the highest standards for...

The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipeline. Responsibilities include: - Acts as a Regulatory Intelligence Triage Manager, responsible for driving...

Beschreibung: We make it GmbH is a nationally active company in Switzerland with a high level of expertise in the field of personnel services thanks to many years of successful experience. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We at it GmbH set the highest...

**Start date**:As soon as possible **Company Overview**: Ikerian AG (formely RetinAI Medical) is a fast-growing medical device software company headquartered in Bern, Switzerland. Our mission is to enable the right decisions sooner in healthcare, through transformative AI & data management solutions for disease screening, monitoring. Join our diverse team...

**Join our team at TechFirm Industrial Services as**: **Operational Project Manager in Manufacturing (w/m/d)** in the GMP environment here in Switzerland! **We are looking for**: - Strong technical background in **chemical engineering** - Significant production experience in the **GMP environment** (chemical, pharmaceutical, ) - Thorough understanding of...

**Join our team at TechFirm Industrial Services as**: **Operational Project Manager in Manufacturing (w/m/d)** in the GMP environment here in Switzerland! **We are looking for**: - Strong technical background in **chemical engineering** - Significant production experience in the **GMP environment** (chemical, pharmaceutical, ) - Thorough understanding of...