Ra Cmc Manager

**Salary**:Competitive - **REF Number**:00055007 - **Consultant**:Katie Genever - **Contact**:+44 01438 870022 - **Date Published**:19.01.2023 - **Sector**: - **Location**:Basel, - **Discipline**: Katie Genever is recruiting for a Regulatory Affairs CMC Associate Manager to join a global healthcare company at their site based in Basel, Switzerland on a...

Basel, Switzerland - 15-06-2023 - JOB TYPE - Permanent - EMP TYPE - Full-Time - EXPERTISE - Regulatory Affairs - SALARY TYPE - Annually - SALARY - Negotiable Position: Head of Regulatory Affairs, CMC & Drug Substances **Responsibilities**: - Establishing and implementing the corporate Regulatory Affairs and CMC development standard across multiple...

Proclinical are recruiting a Director of Regulatory Affairs CMC - CDMO Switzerland for a pharmaceutical consultancy. This role is on a permanent basis and is located in Basel. **Responsibilities**: - Lead the system owners through the issuance, proposal and upkeep of all regulatory documents such as DMF's, CMC documentations for INDs, IMPDs, NDAs, MAAs,...

Proclinical are recruiting a Regulatory Affairs Manager - CMC for a pharmaceutical organisation. This role is on a contract basis and is located in Basel. *** **Responsibilities**: - Offer regulatory assistance for projects and project teams. - Write, evaluate and offer contribution from a CMC perspective on pertinent documents necessary for clinical...

Basel, Switzerland - 14-06-2023 - JOB TYPE - Permanent - EMP TYPE - Full-Time - EXPERTISE - Quality Assurance, Regulatory Affairs - SALARY TYPE - Annually - SALARY - Negotiable **Job Description: QA/RA Manager (Oncology Products)** **Position Overview**: We are seeking a highly skilled and experienced QA/RA Manager to join our pharmaceutical company based...

**At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our...

Job DescriptionContribute to dossier strategy and complex product development plans at a compound level, demonstrating autonomy and accountability.Lead and supervise dossier authoring activities for early and late-stage projects with limited guidance from the manager.Identify areas for business improvement and support the implementation of enhancements under...

**About Abbott** Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Abbott Established Pharmaceuticals (EPD) is looking for a **EM Regulatory Affairs Strategy Lead** for its global Pharma Division Headquarter...

In this role you are responsible for the management of the RA-owned procedural documents and mandatory training for RA GDD worldwide. Your responsibilities include: - Ensure updated and compliant status of RA-owned procedural documents (tracking and coordination of writing) - Support the RA SOPs authors with training and continuous guidance / operational...

**_The Life Science Career Network_** **Technical Regulatory Support Manager -5446** Our client is a pioneer in Drug Discovery and Development and one of the frontrunners in Personalised Healthcare. As the world's largest R&D spender in the pharmaceutical and diagnostics domain, they work in a vast number of drug discovery & therapeutic areas and are...

General Description:_ Associate Director, Supply Chain CMO Management & PM will own and enable the communication, coordinate tasks between the contract manufacturers (CMO) and the functions within the company to meet contract's deliverables, provide services, and keep the relationship positive & on track and deliver performance goals. He/she will also work...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 113,000 colleagues serve people in more than 160 countries.Abbott...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 113,000 colleagues serve people in more than 160 countries. Abbott...

Unsere Mandantin ist ein Schweizer KMU, das sich in einer Nische im Pharmabereich erfolgreich etabliert hat. In ihrem Auftrag suchen wir eine Persönlichkeit mit ausgeprägtem Verantwortungsbewusstsein als Regulatory Affairs Manager Pharma EU/CH (m/w/d). **Arbeitsort**: Grossraum Zürich Aufgaben - Selbständiges Erstellen von...

**CSV Project Manager** **COMPANY** ALTOGEN is a swiss engineering and consulting company specialized in life sciences with proven expertise in pharmaceuticals, biotechnology, medical devices. With several years of experience, technical expertise and project coordination, we support our partners throughout all areas of the product life cycles. We...

**CSV Project Manager** **COMPANY** ALTOGEN is a swiss engineering and consulting company specialized in life sciences with proven expertise in pharmaceuticals, biotechnology, medical devices. With several years of experience, technical expertise and project coordination, we support our partners throughout all areas of the product life cycles. We...

**Why Join Us?** - Be a hero for our rare disease patients_ Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating a supportive and inclusive environment of profound learning and growth - so employees can thrive in all areas of their lives, in and outside...

We have an exclusive mandate for one of our clients in Medical Devices based in Canton of Neuchatel. As a Regulatory Affairs Manager, you will be responsible for: - Support new product development by using in-depth knowledge and understanding of US domestic and international medical device, regulations (including 510k, and International dossiers) - Lead...

**Salary**: CHF120000 - CHF130000 per annum**Job type**: Permanent **Location**: Basel, Schweiz **Function**: Regulatory Affairs, Development **Posted**:22/01/2024 **Ref**: BBBH24375 - Hi I'm Henry , I manage this role Hobson Prior are partnering with a brilliant pharmaceutical organisation who are seeking for an individual to join their team on a...

**Salary**: Highly Competitive Job type: PermanentDiscipline: Project Manager**Location**: Switzerland- Basel, Schweiz - Posting date: 27 Feb 2024 Reference: 57992 Proclinical are recruiting for a Regulatory Affairs Manager - EMEA to join a pharmaceutical organisation. This role is on a permanent basis and is located within the EMEA with the ability to...