Cmc Regulatory Project Coordinator

Regulatory Affairs Manager CMCFor 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 source...

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 submissions to Health...

The Life Science Career NetworkOur 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 world-leading...

Hobson Prior are collaborating with a brilliant pharma establishment who are currently looking for an individual to join their team on a permanent basis located in either Basel or Stockholm. Our client is focused on offering novel remedies that will transform the lives of those suffering from rare illnesses. Th opening position is for a Global regulatory CMC...

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...

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...

Hobson Prior are collaborating with a brilliant pharma establishment who are currently looking for an individual to join their team on a permanent basis located in either Basel or Stockholm. Our client is focused on offering novel remedies that will transform the lives of those suffering from rare illnesses. Th opening position is for a Global regulatory CMC...

**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...

**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...

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 documentation for our...

Posted: Today Location: Basel, Switzerland Job Ref: BH Job Type: Contract Salary:CHF40 CHF44 per hourExpiry date: 1/18/2023 Contact:Audwin CheungXplore 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 contract and you must have valid right...

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 possibleWorkload:100%Location: Basel cityDescription:As Associate Manager within our Global Regulatory Affairs CMC team, you support timely preparation of high-quality CMC (Chemistry,...

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...

**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...

**The Role**: **Here’s What You’ll Do**: Lead a team to develop/implement effective CMC regulatory strategies for submissions (e.g. IND/CTA/BLA/MAA) and identify regulatory risks Provide expertise for regulatory CMC aspects of product development projects Review documents for submission-readiness, to ensure that all submissions conform to health...

**The Role**: **Here's What You’ll Do**: Provide leadership for regulatory CMC aspects of product development projects Lead and drive all CMC submission activities (planning, Review documents for submission-readiness, to ensure that all submissions conform to health authority guidelines Develop effective CMC regulatory strategies for submissions (e.g....

**The Role**: Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners...

The Role:Here's What You'll Do:Provide leadership for regulatory CMC aspects of product development projectsLead and drive all CMC submission activities (planning,Review documents for submission-readiness, to ensure that all submissions conform to health authority guidelinesDevelop effective CMC regulatory strategies for submissions (e.g. IND/CTA/BLA/MAA)...

**The Role**: Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners...

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide,...