Regulatory Compliance Officer

We are looking for a Regulatory Compliance Specialist to join our team in Tolochenaz, Switzerland. As a key member of our quality team, you will be responsible for ensuring the compliance of our processes and products with relevant regulations and standards.In this role, you will work closely with our manufacturing, engineering, and development teams to...

Job Description:The role of Principal Product Compliance Scientist at SICPA involves ensuring the company's products are safe and effective for customers and end-users. This includes creating and aligning regulatory strategies with business goals, identifying regulatory pathways, and preparing strategies for submissions to authorities.A key responsibility is...

We are looking for a Regulatory Compliance Manager to join our team at Panda International. The ideal candidate will possess a strong background in MedTech, FDA regulations, and 510(k) submissions. They should have experience working with Good Manufacturing Practices (GMP) and supporting clinical trials, particularly in Clinical Phase II B.Key...

About MedTech InnovatorWe are dedicated to pushing the boundaries of medical innovation, combining cutting-edge technologies to transform the field of minimally invasive surgery.Our company culture values diversity, inclusivity, and continuous growth, where talented professionals collaborate to drive progress and shape the future of medicine.If you are...

We are seeking a highly motivated and experienced Regulatory Compliance Officer to join our team at Randstad. As a key member of our quality assurance department, you will be responsible for ensuring that our laboratory services meet the highest standards of quality and regulatory compliance.Responsibilities:Maintain Regulatory Compliance: Ensure that our...

At Debiopharm, we strive to make a meaningful impact in the lives of patients by developing innovative therapies for unmet medical needs. Our Quality Management team is responsible for ensuring that our clinical trials meet the highest standards of quality and compliance.Clinical Development Quality LeadKey Responsibilities :The Clinical Development Quality...

Responsibilities and RequirementsThis Senior Regulatory Affairs Specialist role requires a strong background in EU regulations and directives, as well as experience managing regulatory submissions and compliance activities. The ideal candidate will have a minimum of 8+ years of experience in regulatory affairs within the medical device industry, with...

We're passionate about making a difference through minimally invasive care. Our team members are grounded in integrity, have a strong capacity to learn, and bring diverse, real-world experiences to help us think in new ways.Job DescriptionThe Senior Regulatory Affairs Specialist will play a key role in providing advanced regulatory support for NPD and...

About the RoleWe are seeking an experienced Environmental Compliance Specialist to join our team at Intuitive Surgical. As a critical member of our organization, you will play a vital role in ensuring our products and operations comply with European environmental regulations and industry standards.This individual contributor role requires deep regulatory...

Responsibilities:The Principal Product Compliance Scientist at SICPA is responsible for:Developing and implementing regulatory strategies to ensure compliance with relevant regulations.Providing regulatory guidance and support to cross-functional teams.Collaborating with R&D teams to develop innovative products that meet regulatory requirements.Ensuring...

Job OverviewWe are seeking a seasoned Senior Regulatory Affairs Specialist to join our team at Intuitive. This role plays a critical part in providing advanced regulatory support for New Product Development (NPD) and sustaining operations across designated Business Units.Key ResponsibilitiesLead regulatory efforts in NPD projects and sustaining activities,...

As a pioneer in robotic-assisted surgery, we strive to foster an inclusive and diverse team committed to making a difference. We lead with inclusion and empower our team members to do their best work as their most authentic selves.Job RoleThe Senior Regulatory Affairs Specialist will provide advanced regulatory support for NPD and sustaining operations,...

At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a...

Job DescriptionThe Regulatory Affairs Specialist will be responsible for leading substantial and complex regulatory projects, collaborating with management to establish the overall strategic direction for Regulatory Affairs, and ensuring our products and services meet the needs of our patients, customers, regulators, and remain compliant with our internal...

Company Overviewembecta is a leading global diabetes care company dedicated to empowering people with diabetes to live their best life through innovative solutions and partnerships.Job DescriptionThe Global Customs Analyst will provide critical support for Customs and trade compliance matters across multiple regions, working closely with regional teams to...

At Intuitive Surgical, we're dedicated to advancing minimally invasive care. As a pioneer in robotic-assisted surgery, we strive to foster an inclusive and diverse team committed to making a difference.Job OverviewThe Senior Regulatory Affairs Specialist plays a critical role within the Regulatory Affairs Department, focusing on providing advanced regulatory...

Source Technology is hiring a GMP Compliance Manager to ensure our CAPEX projects meet regulatory requirements. As a key member of our team, you will be responsible for managing risks and developing strategies to maintain compliance.Key Responsibilities:Develop and implement compliance strategies to ensure regulatory adherence.Collaborate with internal...

About ONWARD (GTX Medical)We are committed to developing innovative medical systems for individuals with spinal cord injuries. As a Software Quality Engineer at ONWARD, you will play a critical role in ensuring the production and delivery of high-quality medical systems.Key Job ResponsibilitiesDevelop Quality Strategy: Develop a quality strategy to ensure...

About the RoleThis Senior Regulatory Affairs Specialist position is responsible for providing advanced regulatory support for NPD and sustaining operations across designated Business Units. The ideal candidate will have a deep understanding of EU regulations and directives, as well as experience managing regulatory submissions and compliance activities.Key...

Environmental Compliance SpecialistJoin our dynamic team at Intuitive Surgical as an Environmental Compliance Specialist! In this critical role, you will ensure our products and operations comply with European environmental regulations and industry standards.This individual contributor role requires deep regulatory expertise, analytical skills, and the...