Technical Regulatory Support 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...

Proclinical are recruiting for a Regulatory Technical Manager for a pharmaceutical organisation. This role is on a contract basis and is located in Basel. *** **Responsibilities**: - Accountable for preparation and upkeep of CMC documentation in internal document management systems and assist with associate actions. - Handle regulatory changes throughout...

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...

**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...

**Your mission** To strengthen their team, they are looking **for a Quality & Regulatory Affairs Manager (80% - 100%). based in Neuchâtel.** **Tasks are the following**: **Quality Management** - Further development and implementation of quality management - Deputy to the Quality Management Representative - Conduct internal audits as per audit program -...

**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...

**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...

**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...

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...

Posted: - Today- Location: - Basel, Switzerland- Job Ref: - BH-34786- Job Type: - Contract- Salary: - CHF40 - CHF44 per hour- Expiry date: - 1/18/2023- Contact: - Audwin Cheung- Xplore Life Sciences are recruiting for an Associate Regulatory Affairs CMC Manager to work for a Global Leader in Pharmaceuticals based in Basel. This is an 18 Month freelance...

**For our client, a leading pharma company in Basel, we are looking for a Regulatory Affairs CMC Associate Manager to start asap.** **Your mission** As Associate Manager within our Global Regulatory Affairs CMC team, you support timely preparation of high-quality CMC (Chemistry, Manufacturing, and Control) regulatory documentation for our products and...

**Posted date **15 April 2024 **Location**Basel **Job type** Permanent **Salary**Negotiable **Discipline** Life Sciences **Reference**JO-2404-533260 **Work Location** Hybrid An exciting and growing business looking to bring state-of-the-art medical technology to the market, enabling people globally to self-manage diabetes and other chronic diseases,...

**For our client, a leading pharma company in Basel, we are looking for a Regulatory Affairs CMC Associate Manager to start asap.** **Contract duration**: 18 months with extension possible **Workload**:100% **Location**: Basel city **Description**: As Associate Manager within our Global Regulatory Affairs CMC team, you support timely preparation of...

Job PurposeBe 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 ResponsibilitiesSupport product development process and ensure compliance of deliverablesCompile the Regulatory...

Job PurposeBe 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 ResponsibilitiesSupport product development process and ensure compliance of deliverablesCompile the Regulatory...

**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...

ABOUT ARCONDIS Arcondis is a global consulting company with an exclusive focus on the healthcare and life science industries, with their particularly demanding requirements on quality and regulatory aspects. We have been managing challenges and solving problems for our clients in the areas of compliance, business processes, information technology, and...

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...

**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 including Computerized...

For our customer located in Basel/Switzerland we are currently looking for a**: Regulatory Affairs CMC Manager **(M/F/x) **Tasks & Responsibilities / Must Haves** - Responsible for regulatory activities specifically related to chemistry, manufacturing, and control (CMC). Activities such as the preparation & publication of REG CMC documentation for...