Regulatory Compliance Expert in Pharmaceutical Manufacturing

About the RoleAs a Quality Assurance Manager at Roche, you will play a critical role in ensuring the delivery of Investigational Medicinal Products (IMPs) to our patients in compliance with current Good Manufacturing Practices (cGMP). You will be responsible for providing quality and compliance oversight of all manufacturing units and clinical packaging in...

Job DescriptionAbout the RoleThe Senior Manager of GMP/GDP Quality Compliance will play a critical role in ensuring the regulatory compliance status of BeiGene and its vendors. This position requires a strong understanding of global regulatory and health authority requirements, as well as excellent communication and interpersonal skills.Key...

Stratpharma AG, a leading pharmaceutical company, is seeking a highly skilled Quality Assurance and Regulatory Associate to join their team. This is a challenging global role that will work closely with the International Quality Assurance and Regulatory Director in managing the company's global quality assurance and regulatory functions.This is a highly...

Job SummaryWe are seeking a highly experienced and skilled Head of International Regulatory Affairs and Compliance to join our team at Ironwood Pharmaceuticals. This is a critical role that will lead our global regulatory strategy and ensure compliance with all applicable regulations.Key ResponsibilitiesDevelop and Implement Regulatory Strategy: Develop and...

About the RoleIn this position, you will be working in the Synthetic Molecules Technical Development team at Roche. This team brings a broad range of experience across drug substance, drug product, analytical sciences, and manufacturing science & technology, and collaborates closely with key partners in Research and Early Development as well as with our...

About Mepha and Teva in SwitzerlandMepha Pharma AG and Teva Pharma AG are two leading pharmaceutical companies in Switzerland, operating together as a single entity. Since 2011, Mepha has been part of the internationally active Teva Group, one of the world's leading suppliers of generic medicines. Our companies are based in Basel and employ a total of 174...

Job OverviewAmaris Consulting is seeking a skilled Manufacturing Operator to join our team. As a key member of our production team, you will play a vital role in ensuring the efficient and compliant execution of manufacturing processes.Key ResponsibilitiesProcess Execution: Prepare, execute, and complete manufacturing tasks efficiently and in compliance with...

About the RoleWe are seeking a highly experienced and skilled Senior Quality Assurance Manager to lead our Quality Systems and Compliance team at our Basel Drug Substance Manufacturing site. As a key member of our Quality organization, you will be responsible for ensuring regulatory compliance and providing strategic direction for regulatory inspections and...

About the RoleRoche is a global leader in the pharmaceutical industry, committed to fostering diversity, equity, and inclusion in all aspects of our business. As a key player in the healthcare sector, we recognize the importance of diversity in driving success and delivering exceptional care to our customers.The Pharma Technical Operations (PT) Global MSAT &...

About the RoleWe are seeking a highly skilled Quality Assurance Manager to join our team at Gi Group SA. As a Quality Assurance Manager, you will be responsible for ensuring the quality and compliance of our pharmaceutical products.Key ResponsibilitiesSupport and drive the implementation of Annex 1 requirements in our Clinical Supply Centre for sterile Drug...

About Mepha and Teva in SwitzerlandMepha Pharma AG and Teva Pharma AG are two leading pharmaceutical companies in Switzerland, operating together as a single entity. Since 2011, Mepha has been part of the internationally active Teva Group, one of the world's leading suppliers of generic medicines. Our companies are based in Basel and employ a total of 174...

About the RoleWe are seeking a highly skilled Quality Assurance Manager to join our team at Gi Group SA. As a key member of our Quality Operations Unit, you will be responsible for ensuring the quality and compliance of our Investigational Medicinal Products (IMPs) manufactured and packed for clinical studies in Switzerland.Key ResponsibilitiesImplementation...

About the RoleIn this position, you will be working in the Synthetic Molecules Technical Development team at Roche, a leading pharmaceutical company. This team brings a broad range of experience across drug substance, drug product, analytical sciences, and manufacturing science & technology, and collaborates closely with key partners in Research and Early...

Stratpharma AG, a leading pharmaceutical company, is seeking a highly skilled Quality Assurance and Regulatory Associate to join their team. This is a challenging global role that will work closely with the International Quality Assurance and Regulatory Director in managing the company's global quality assurance and regulatory functions.This is a highly...

Stratpharma AG, a leading pharmaceutical company, is seeking a highly skilled Quality Assurance and Regulatory Associate to join their team. This is an exciting opportunity to work closely with the International Quality Assurance and Regulatory Director in managing the company's global quality assurance and regulatory functions.This is a highly successful...

Job DescriptionAbout the RoleThe Senior Manager of GMP/GDP Quality Compliance will play a critical role in ensuring the regulatory compliance status of BeiGene and its vendors. This position requires a highly motivated and collaborative individual with a strong understanding of global regulatory and health authority requirements.Key ResponsibilitiesExecute...

About the RoleAs a Senior Consultant MES Expert at ARCONDIS, you will play a key role in managing and coordinating projects in the Manufacturing of Pharma and/or MedTech clients. Your primary responsibility will be to deliver successful consulting and solution engagements with manufacturing clients, focusing on the implementation and optimization of MES and...

About the RoleAs a Clinical Trial Regulatory Lead at Roche, you will play a critical role in shaping the company's regulatory strategy for clinical trials globally. This is an exciting opportunity to work with a dynamic team and contribute to the development of life-changing therapies.Key ResponsibilitiesDevelop and implement regulatory strategies for...

About D-ployD-ploy is a leading provider of IT and Engineering Solutions, serving clients across the EMEA region and the USA. Our company prides itself on delivering innovative and superior services and solutions to numerous industry-leading clients.We build trusted partnerships within the IT community, optimizing our customers' IT productivity and...

About the RoleAs a Senior Consultant MES Expert at ARCONDIS, you will play a key role in managing and coordinating projects in the Manufacturing of Pharma and/or MedTech clients. Your primary responsibility will be to deliver successful consulting and solution engagements with manufacturing clients, focusing on the implementation and optimization of MES and...