Regulatory Auditor for Biologics and Small Molecules

OverviewLundbeck is a global pharmaceutical company dedicated to transforming lives through innovative treatments for brain diseases. Our team of experts in Process Chemistry R&D is seeking a highly skilled Lead Synthetic Chemist to join our dynamic team.Job SummaryWe are looking for an experienced synthetic organic chemist to lead the development of new...

GMP/GDP Auditor Role OverviewThis is a great opportunity for an international position as GMP/GDP auditor in CMC Development QA, supporting the development of new innovative treatments for brain diseases. You will have an important role as lead auditor conducting external audits of CMC vendors as well as internal audits of CMC. We offer an exciting job,...

GMP/GDP Auditor, CMC Development QA RoleThis is an exciting opportunity for an international position as a GMP/GDP auditor in CMC Development QA, supporting the development of new innovative treatments for brain diseases. As a lead auditor, you will have an important role conducting external audits of CMC vendors as well as internal audits of CMC. We offer a...

Role SummaryLundbeck seeks a highly skilled GMP/GDP Auditor to join its CMC Development QA team. As a key member of this team, you will play a vital role in ensuring the quality and compliance of our CMC vendors.Key ResponsibilitiesConduct external audits of CMC vendors to ensure compliance with GMP/GDP regulationsLead internal audits of CMC to identify...

GMP/GDP Auditor, CMC Development and Quality Assurance Specialist This is an exciting opportunity for an international position as a GMP/GDP auditor in CMC Development and Quality Assurance, supporting the development of new innovative treatments for brain diseases. In this role, you will have a vital part as a lead auditor conducting external audits of...

About Ferring PharmaceuticalsFerring Pharmaceuticals A/S is a global company that helps people build families and live better lives. We are committed to scientific advances in reproductive and women's health, gastroenterology, and urology.Job Title: CMC Regulatory Expert - Product LifecycleWe are seeking an experienced Global Regulatory Affairs Manager to...

This role offers a unique opportunity to join Lundbeck's CMC Development QA team as a GMP/GDP Auditor.About the RoleAs a GMP/GDP Auditor, you will be responsible for conducting external audits of CMC vendors and internal audits of CMC. You will also contribute to the continuous improvement of the audit process.Key ResponsibilitiesConduct external audits of...

GMP/GDP Auditor, CMC Development QA SpecialistThis is an exciting opportunity to join our team as a GMP/GDP auditor in CMC Development QA, supporting the development of new innovative treatments for brain diseases. You will have a key role as lead auditor conducting external audits of CMC vendors as well as internal audits of CMC. We offer a challenging job,...

GMP/GDP Auditor, CMC Development QA RoleThis is a great opportunity for an international position as GMP/GDP auditor in CMC Development QA, supporting the development of new innovative treatments for brain diseases. You will have an important role as lead auditor conducting external audits of CMC vendors as well as internal audits of CMC. We offer an...

GMP/GDP Auditor, CMC Development QAThis is an exciting opportunity for a professional to join our team as a GMP/GDP auditor in CMC Development QA, supporting the development of new innovative treatments for brain diseases. As a lead auditor, you will have an important role in conducting external audits of CMC's vendors as well as internal audits of CMC.Your...

Senior Regulatory Scientist RoleWe are continuing to grow our Nordic business and are now seeking a Senior Regulatory Scientist. This role is suitable for those who are excited at the pace of change and innovation in Life Science, who want to partner with cutting-edge clients and continuously learn, develop, and progress personally and professionally.Key...

**About the Role**We are seeking a seasoned Senior Regulatory Scientist to spearhead our regulatory affairs efforts in the Nordic region. This is an excellent opportunity for individuals who thrive in dynamic environments and are passionate about driving innovation in Life Science.**Responsibilities:**Develop and execute regulatory strategies for assigned...

Senior Regulatory ScientistWe are seeking a highly skilled Senior Regulatory Scientist to join our team at Voisin Consulting SARL. This role will involve developing and executing regulatory strategies for assigned projects, including the preparation and submission of regulatory filings.Key Responsibilities:Develop and execute regulatory strategies for...

About this roleGMP/GDP Auditor, CMC Development QAThis is a fantastic opportunity for a skilled auditor to support the development of innovative treatments for brain diseases. As a GMP/GDP auditor, you will play a crucial role in conducting external audits of CMC vendors and internal audits of CMC, ensuring compliance with regulatory requirements.As a key...

Senior Regulatory Scientist RoleWe are expanding our business and seeking experienced Senior Regulatory Scientists to work with cutting-edge clients in the Life Sciences industry.This consulting role is ideal for individuals who bring deep regulatory expertise, have commercial acumen, and can provide strategic advice and build strong client relationships.The...

Regulatory Affairs SpecialistWe are seeking an experienced Regulatory Affairs Specialist to join our team at VCLS. As a key member of our regulatory team, you will play a critical role in ensuring that our clients' products meet the latest regulatory requirements.Your primary responsibilities will include:Developing and implementing regulatory strategies for...

Senior Regulatory Scientist (Consultant)We are expanding our business and seeking experienced Senior Regulatory Scientists who are passionate about the evolving Life Sciences industry and excited by the opportunity to work with cutting-edge clients. This consulting role is ideal for individuals who not only bring deep regulatory expertise but also have the...

Unlock Your Potential as a Clinical Biomarkers SpecialistLundbeck is seeking a highly skilled Clinical Biomarkers Specialist to join our team in Valby, Denmark. As a key member of our Clinical Biomarkers team, you will play a critical role in developing and validating biomarker assays for clinical trials.About the RoleLead the development and validation of...

Unlock Your Potential as a Clinical Biomarkers SpecialistLundbeck is seeking a highly skilled Clinical Biomarkers Specialist to join our team in Valby, Denmark. As a key member of our Clinical Biomarkers team, you will play a critical role in developing and validating biomarker assays for clinical trials.Your Key ResponsibilitiesLead the development and...

Quality Assurance Specialist, CMCLeverage your expertise in quality assurance to support the development of new treatments for brain diseases at Lundbeck. As a Quality Assurance Specialist, CMC, you will ensure patient safety and GMP compliance of Investigational Medicinal Products (IMPs) for clinical trials.Your Key ResponsibilitiesReview batch records to...