Cmc Dossier Manager
Vor 3 Tagen
**CMC Dossier Manager**
The CMC Dossier Manager works in the Sobi Technical Operations Department within in the CMC Program Management unit. The role is responsible for technical oversight and the coordination of generation of CMC documentation. Within the scope is the source documentation for process development, process validation, GMP and non-GMP manufacture of drug substance, drug product and finished product, both for clinical and marketed products from a regulatory perspective. The Dossier Manager will coordinate between SME’s, Global Regulatory Affairs and External Manufacturing and Development organizations to ensure in-time generation of high-quality CMC modules for development products. The CMC Dossier Manager role also entails the support of CMC variations, Health Authority requests and the Life Cycle Management for the global expansion of Sobi’s marketed product portfolio.
**Key responsibilities**
- Provide leadership to ensure development and life-cycle management of Sobi’s products from a technical and regulatory perspective.
- Compile sections of the Module 3 and 2.3 as required.
- Support meetings with Regulatory Agencies (Advice Meetings, Pre-Filing and others) and manage negotiations to resolve CMC issues. Provide support for preparation of meetings with Health Authorities including preparation of briefing packages.
- Liaise with Global Regulatory functions and partner organizations or external consultants as appropriate.
**Qualifications**
- Master’s in Biotechnology, Chemistry, Pharmacy or equivalent and strong knowledge in scientific and technical aspects of pharmaceutical development and manufacturing in a GMP environment.
- 8 years plus of experience in CMC development activities for Biologics and/or Small Molecules.
- 5 years plus experience in regulatory aspects regarding Chemistry, Manufacturing and Control of Manufacture as well as development.
- Excellent project management skills, attention to detail and the ability to manage a team.
- Effective verbal and written communication skills.
- Good level of oral and written English
- Good knowledge of cGMP's and the know-how to work and manage within the highly regulated pharmaceutical environment.
**Personal attributes**
- Strong leadership qualities including strategic thinking, communication, organization and out-of-the-box thinking.
- Able to identify problems and implement solutions in ambiguous environment.
- Able to balance and communicate risks appropriately.
- Able to convince internal and external partners.
- Good organizational and communication skills, both written and oral skills, and “do-what-it-takes” attitude.
- Independently motivated, detail-oriented and good problem-solving ability.
- Excellent organizational skills, sufficient to multi-task in an extremely fast-paced environment In addition, you must demonstrate behaviors in line with Sobi's core values: Care, Ambition, Urgency, Ownership and Partnership.
**Location**
The position will be based in Basel, Switzerland
**Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services to them. Our employees come from a variety of backgrounds within research, healthcare, industry and the academic sphere.**
**Sobi is an affirmative action and equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, disability, age, sexual orientation, gender identity, or national origin. Sobi is committed to providing access, equal opportunity and reasonable accommodation for individuals with disabilities in employment, its services, programs and activities.**
**Why Join Us?**
We are a global company with around 1,500 employees in more than 30 countries, and are committed to the societies where we operate. With a deeply skilled management team directing our day-to-day wins, and a Board with a stellar track record, we’re ready to take on the world’s diseases, ailments and adversity. Our people believe they have the power to make a positive impact in others’ lives because that’s exactly what we do here. If you’re seeking a career that taps into your talents in a way that makes the world a better, healthier place, we just may have a job for you.
We know our employees are our most valuable asset, and our culture conveys that. We offer a competitive benefits package, to support the health and happiness of our staff.
**Sobi Culture**
At Sobi, we refuse to accept the status quo. This is because we have witnessed first-hand the challenges facing those affected by rare diseases, and have used this knowledge to shape our business to find new ways of helping them.
As a specialized biopharmaceutical company, we are dedicated to rare diseases. And we see this focus as a strength. By effectively turning our research into ground-breaking trea
-
Senior Manager – CMC Dossier Manager
Vor 3 Tagen
Basel, Schweiz Aixial Group VollzeitSenior Manager – CMC Dossier Manager (M/F) Location : Basel, Switzerland 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...
-
Regulatory Affairs Manager
Vor 7 Tagen
Basel, Schweiz Proclinical VollzeitProclinical 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...
-
Regulatory Affairs Manager
Vor 7 Tagen
Basel, Schweiz Thermo Fisher Scientific VollzeitCMC Expert - Client Dedicated (Regulatory CMC - Biologics) We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we...
-
Sr. Manager, Cmc Regulatory Science
Vor 4 Tagen
Basel, Schweiz Moderna Vollzeit**The Role**: **Here’s What You’ll Do**: Develop effective CMC regulatory strategies for submissions (e.g. IND/CTA/BLA/MAA) and identify regulatory risks Provide guidance for regulatory CMC aspects of product development projects Review documents for submission-readiness, to ensure that all submissions conform to health authority guidelines Contribute...
-
Sr. Manager, Cmc Regulatory Science
Vor 7 Tagen
Basel, Schweiz Moderna Therapeutics Vollzeit**The Role**: **Here’s What You’ll Do**: Develop effective CMC regulatory strategies for submissions (e.g. IND/CTA/BLA/MAA) and identify regulatory risks Provide guidance for regulatory CMC aspects of product development projects Review documents for submission-readiness, to ensure that all submissions conform to health authority guidelines Contribute...
-
Senior Manager – CMC Dossier Manager
Vor 2 Tagen
Basel, Schweiz TN Switzerland VollzeitClient:Aixial GroupLocation:Job Category:OtherJob Reference:90452fb773fdJob Views:10Posted:24.01.2025Job Description:Who is Aixial Group?Aixial Group is 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...
-
Manager, Regulatory Affairs
Vor 6 Tagen
Basel, Schweiz Lonza VollzeitTitle: Manager, Regulatory Affairs (CMC)Hybrid working pattern: 2 WFHLocation: Basel or VispRelocation 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 people working...
-
Sr. Manager International Operations
Vor 5 Tagen
Basel, Schweiz Moderna Therapeutics Vollzeit**The Role**: This role is an exciting opportunity to be part of a growing CMC international organization, responsible for the manufacturing and supply of Moderna’s COVID mRNA vaccine internationally, as well as preparation for commercial manufacturing for further projects coming via our pipeline. Reporting to the Director, International Operations, the...
-
Ra Manager
vor 1 Woche
Basel, Schweiz Proclinical Staffing VollzeitProclinical is seeking a Regulatory Affairs Manager to join our client's team in Basel, Switzerland. This role focuses on supporting regulatory submissions for biological medicinal products within the dermatology sector. You will play a crucial role in ensuring compliance and facilitating communication with health authorities. Please note that to be...
-
Regulatory Affairs Manager
Vor 3 Tagen
Basel, Schweiz TN Switzerland VollzeitSocial network you want to login/join with:Responsibilities:Author and review CTD module 3.2 sections (drug substance/ drug product) for biological medicinal products;Prepare high-quality clinical trials applications, BLA/ MAA, and post-approval submissions;Manage timely responses to Health Authority (HA) questions;Lead and coordinate activities to ensure...
-
Regulatory Affairs Manager
Vor 6 Tagen
Basel, Schweiz CTC Resourcing Solutions VollzeitThe Life Science Career NetworkCTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes.Our client, a global market leader in the production and process...
-
Associate Director Global Cmc Quality Operations
vor 9 Stunden
Basel, Schweiz Moderna Therapeutics Vollzeit**The Role**: Reporting to the Director, Product Quality Lead the Associate Director, Product Quality Lead will be responsible for developing, approving, monitoring and maintaining critical quality standards, identifying quality risks, ensuring quality management of product and processes lifecycle, leading improvement and alignment with current regulatory...
-
RA Manager, Basel
Vor 3 Tagen
Basel, Schweiz TN Switzerland VollzeitProclinical is seeking a Regulatory Affairs Manager to join our client's team in Basel, Switzerland. This role focuses on supporting regulatory submissions for biological medicinal products within the dermatology sector. You will play a crucial role in ensuring compliance and facilitating communication with health authorities.Please note that to be...
-
QA Manager GMP/GDP
vor 1 Woche
Basel, Schweiz CTC Resourcing Solutions VollzeitQA Manager (GMP/GDP) – 6166 ADAOur client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking for a QA Manager with GMP and/or GDP experience for 1 year contract with high possibility of extension based in...
-
QA Manager GMP/GDP, Basel
Vor 3 Tagen
Basel, Schweiz TN Switzerland VollzeitSocial network you want to login/join with:Responsibilities:Provide GMP/GDP quality assurance expertise during development and commercialization of client’s products.Ensure all required quality activities are initiated and completed according to the development stage.Ensure that medicinal products are designed, developed, manufactured and controlled...
-
Technical Regulatory Support Manager
Vor 3 Tagen
Basel, Schweiz CTC Resourcing Solutions Vollzeit**_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...
-
QA Manager
vor 2 Wochen
Basel, Schweiz Idorsia Pharmaceuticals Ltd. Vollzeit**About Idorsia Pharmaceuticals Ltd** Idorsia Ltd is reaching out for more - We have more ideas, we see more opportunities and we want to help more patients. In order to achieve this, we want to develop Idorsia into one of Europe’s leading biopharmaceutical companies, with a strong scientific core. Headquartered in Switzerland - a European biotech hub -...
-
Senior Process Manager
Vor 6 Tagen
Basel, Basel-Stadt, Schweiz Sobi VollzeitCompany OverviewSobi is an international pharmaceutical company focused on specialty pharmaceuticals. We cater to the high medical needs of rare disease patients and provide treatment and services to them.Job DescriptionWe are seeking a Senior Process Manager to join our team. As a key member of our Global CMC, Science & Technology Department, you will be...
-
Technical Regulatory Support Manager
Vor 3 Tagen
Basel, Schweiz GITR Vollzeit**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...
-
Sr. Manager, Regulatory Compliance
vor 9 Stunden
Basel, Schweiz Moderna Therapeutics Vollzeit**The Role**: Reporting to the Director Quality Systems & Compliance the Snr Manger/AD Regulatory Compliance will be responsible to be the liaison function between Quality and the Regulatory CMC functions of Moderna. The role will implement and continuously improve required processes to ensure the compliance of Moderna’s product with the registered...