Regulatory Technical Manager

**EINFÜHRUNG**: As a preferred supplier for Roche in Basel, we are looking for an individual as **Technical Regulatory Support Manager**: with contract for 1 year. The earliest start date is within 2 months. Home Office will be possible for max. 2 days a week. **AUFGABENBESCHREIBUNG**: - Proactively support the technical regulatory department on the...

**_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...

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...

For our client, an international pharmaceutical company in Zurich, we are in search for a **Senior Regulatory CMC Manager (f/m/d).** **Responsibilities**: - Prepare CMC responses to health authority questions during development, registration and product lifecycle - Identify the required documentation for global submissions and negotiate the delivery of...

For our client, an international pharmaceutical company in Basel, we are in search for a **Senior Regulatory CMC Manager (f/m/d).** **Responsibilities**: - Prepare CMC responses to health authority questions during development, registration and product lifecycle - Identify the required documentation for global submissions and negotiate the delivery of...

**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...

**The Life Science Career Network** Our client is a leading global player in the Pharmaceutical industry with global headquarters in Basel, Switzerland. They are undergoing a transformation with respect to culture and outside perception. The organisation focusses on novel therapies in Oncology and Ophthalmology and is also currently developing a...

Location: role can be located anywhere in Europe At Corza Medical, our mission is to support surgical providers with remarkable service, trusted performance, and outstanding value by creating an unmatched experience that stems from listening to the surgical experts themselves. Our product family is the result of years of experience championing surgeons and...

**Arxada** is a pioneering leader with a powerful legacy**:Over 120 years **of creating specialty chemicals and solutions that potentiate the performance of our customers and their products. Our solutions, our expertise and our support help them to perform better - to be more efficient, more effective and more sustainable. We are passionate about empowering...

EUMEDICA Pharmaceuticals AG is an independent and privately owned pharmaceutical company founded in 1986 in the heart of Basel, Switzerland.Our responsibility is to ensure continuity of access to patients and healthcare professionals to our unique and targeted therapeutic solutions portfolio.We focus on niche, severe pathologies, and therapeutic...

About UsExponent is a global leader in providing expert consulting services to clients in the industrial chemicals sector. Our team of experts has extensive experience in managing regulatory projects and providing technical and regulatory consultancy services.Job DescriptionThe successful candidate will be responsible for managing REACH regulatory projects,...

Regulatory Affairs Manager CMC For our client in Basel, we are looking for RA CMC Manager who will be responsible for global CMC submission activities for assigned projects. **Responsibilities**: - Identify the required documentation and any content, quality and/or timeliness issues for global submissions and negotiate the delivery of approved technical...

**The Role**: The Regulatory Operations Submission Manager is responsible for the planning, managing and tracking of regulatory submissions. In collaboration with the Regulatory Lead, he/she plans and prepares high quality global submissions, in-house or via CRO, ensuring delivery of compliant submissions to global health authorities in a timely manner. The...

In this critical role, you will lead a portfolio of IT infrastructure projects, ensuring alignment with strategic business goals, objectives, and adherence to the overall program management methodologies.You will identify, evaluate, and manage program-level risks and issues, developing robust mitigation strategies to address technical, regulatory, and...

**Quality Assurance & Regulatory Affairs (QA/RA) Manager - Medical Devices** 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...

For our customer located in Basel/Switzerland we are currently looking for a**:Regulatory Affairs CMC Associate Manager **(M/F/x)** - * pay rate range - given by our client: 51 chf/h* * Hiring Manager Job Description: * - As Associate Manager within our Global Regulatory Affairs CMC team, you support timely preparation of high quality CMC regulatory...

Manager Scientific Regulatory Strategy - Neuchatel, Switzerland Be a part of a revolutionary change. At PMI, we’ve chosen to do something incredible. We’re totally transforming our business, and building our future on smoke-free products. With huge change, comes huge opportunity. So, wherever you join us, you’ll enjoy the freedom to dream up and...

**Job Purpose** Be a member of product development project-teams from the initiation phase, ensure implementation of quality and Regulatory Affairs requirements for Europe, US & Canada, perform product registration in EU, US & Canada. **Main Tasks and Responsibilities** - Support product development process and ensure compliance of deliverables - Compile...

Title : Manager, Regulatory Affairs (CMC) Hybrid working pattern : 2 WFH Location : Basel or Visp Relocation support is provided – subject to criteria. Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented...

**Technical QA Manager** **Technical QA Manager (M/F/d) - GMP / Pharma / Qualification / Validation / CSV** **Projekt**: For our client, a big pharmaceutical company in Basel we are looking for Technical QA Manager (M/F/d). **Background**: **Tasks & Responsibilities**: - Running, maintaining and continuously improving Qualification/Validation activities...