Head of Cmc/cmc-qa

GRANITE BIO is a recently established biotechnology company in the Ridgeline Discovery incubator located in Basel (Switzerland). Based on fundamental research over the last two decades, GRANITE BIO’s differentiated approach is to impact central disease biology nodes to transform inflammatory, autoimmune and fibrotic conditions. The lead therapeutic...

GRANITE BIO is a recently established biotechnology company in the Ridgeline Discovery incubator located in Basel (Switzerland). Based on fundamental research over the last two decades, GRANITE BIO’s differentiated approach is to impact central disease biology nodes to transform inflammatory, autoimmune and fibrotic conditions. The lead therapeutic...

GRANITE BIO is a recently established biotechnology company in the Ridgeline Discovery incubator located in Basel (Switzerland). Based on fundamental research over the last two decades, GRANITE BIO’s differentiated approach is to impact central disease biology nodes to transform inflammatory, autoimmune and fibrotic conditions. The lead therapeutic...

**CMC Regulatory Project Coordinator** You will be repsonsible for coordinating the budget of the CMC development activities of the late stage phase within the CMC Development organization. You will collaboaret with internal and external partners to support deliverables according to project timelines and defined budget. **Responsibilities**: - Monitoring...

Job Title: CMC Technical Dossier ManagerJoin our team as a CMC Technical Dossier Manager and take on a challenging role that requires strong technical expertise and leadership skills.About the Role:We are seeking a highly skilled and experienced CMC Technical Dossier Manager to join our team. As a key member of our CMC Dossier Management team, you will be...

Job Title: CMC Technical Dossier ManagerJoin Dova Pharmaceuticals as a CMC Technical Dossier Manager and take on a challenging role that requires strong technical expertise and excellent communication skills. As a key member of our team, you will be responsible for developing and managing technical eCTD sections to support regulatory CMC dossier...

Job SummaryGenentech is seeking a highly skilled External CMC Collaboration Lead to join our team. As a key member of our organization, you will be responsible for ensuring the successful planning and execution of outsourced activities supporting Chemistry Manufacturing Controls (CMC) deliverables for Roche's clinical pipeline in Biologics/Novel technologies...

Job Description SummaryOur Development Team is guided by our purpose: to reimagine medicine to improve and extend people's lives. To achieve this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities – all to bring our medicines...

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...

Job Description SummaryOur Development Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives.To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities – all to bring our medicines to...

Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives.To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities – all to bring our medicines to patients even faster.We...

**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 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....

Aixial Group, a leading CRO (Clinical Research Organization), is seeking a seasoned Senior Manager to lead our CMC Dossier Manager team. Located in Basel, Switzerland, this role will be part of our Life Science division, specializing in providing technical support for clinical projects from phases I to IV and post-market.With over 9 years of experience in...

**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 Position Roche’s CDMO Organization interfaces with 80+ contract development and manufacturing organizations (CDMOs) around the world to boost the capacity and capabilities of the supply network as our portfolio evolves. CDMO prioritizes speed, quality and cost with our CDMO partners to deliver clinical materials and 55 product families to more than 70...

**Who is Aixial Group ?** Aixial Group, we are a CRO (Clinical Research Organization), specialized in Life Science. We work with laboratories to provide technical support on clinical projects from phases I to IV and post market. Since 2014, we have been part of the Alten family. We are developing our activities in Switzerland, France, Belgium, Czech...

CMC Technical Writer – DP Drug Product Lyophilization PositionWe are seeking a skilled CMC Technical Writer to join our team at Aixial Group.As a CMC Technical Writer, you will be responsible for creating high-quality documentation related to drug product lyophilization processes.Key responsibilities include:Developing and maintaining technical...

CMC Technical Writer - DP Drug Product LyophilizationAt Aixial Group, we are seeking a skilled CMC Technical Writer to join our team in Basel, Switzerland. As a CMC Technical Writer, you will be responsible for creating high-quality technical documents for our drug product lyophilization projects.Key Responsibilities:Develop and maintain technical documents,...

Senior Manager – CMC Dossier ManagerLocation: Basel, SwitzerlandAixial Group is a CRO (Clinical Research Organization) specializing in Life Science.We work with laboratories to provide technical support on clinical projects from phases I to IV and post-market.Our team is developing activities in Switzerland, France, Belgium, Czech Republic, Denmark, UK,...