Quality and Regulatory Systems Development Specialist

The Opportunity:Avantor is seeking a skilled professional to develop and implement systematic solutions that address the complex business challenges of global Quality and Regulatory business users. The ideal candidate will provide necessary support to ensure systems are available and functioning properly during operational hours, focusing on areas such as...

Job OverviewMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly motivated Regulatory Compliance Specialist to join our team. As a key member of our clinical development team, you will be responsible for ensuring compliance with regulatory requirements and guidelines in the assigned countries.Key Responsibilities:Maintain awareness of...

At Avantor, we are committed to helping you grow your career through our diverse and inclusive culture. We offer a wide range of opportunities for professional development and advancement.About the RoleWe are seeking an Advanced Quality Systems Specialist - Global Regulatory Expert to join our team in Mexico City, MEX. This is a full-time position that will...

Job SummaryA Quality Systems Supervisor at Medtronic is responsible for ensuring the development and maintenance of quality programs, systems, processes, and procedures that meet internal and external standards.The ideal candidate will have expertise in interpreting policies, regulatory, and governmental regulations, and internal regulations to assure...

Job SummaryWe are seeking a highly skilled Compliance Content Manager and Regulatory Specialist to join our team at ERM Libryo. This is a unique opportunity to work with a leading compliance platform that helps global organizations navigate their regulatory requirements.About the RoleThe successful candidate will be responsible for managing and maintaining...

About the OpportunityAvantor, a global leader in the life sciences industry, is seeking a Quality Expert with Regulatory Compliance expertise to join its team.The Role:This is an exciting opportunity for a seasoned Quality Expert to work closely with cross-functional teams to ensure compliance with regulatory requirements and industry standards. The...

About the Opportunity">Avantor is seeking a highly skilled Quality, Trade and Regulatory System Export to join its Information Technology department. This role will involve working closely with global Quality and Regulatory business users to develop and implement systematic solutions that address their most complex challenges.The successful candidate will...

Regulatory & Start Up SpecialistWe are seeking a skilled Regulatory & Start Up Specialist to join our cFSP team in a Home Based role.Location: Argentina & MéxicoJob Summary:We are looking for a detail-oriented and organized Regulatory & Start Up Specialist to perform site activation activities in accordance with local and international regulations, standard...

Rivka Development is seeking a skilled Software Development Specialist to join our team. As a key member of our development team, you will be responsible for designing, developing, and maintaining scalable software applications using TypeScript/Javascript (Angular or React).Key Responsibilities:Develop high-quality front-end software applications, ensuring...

We are looking for a highly skilled Regulatory and Compliance Specialist to join our team in a Home Based role. This role will focus on performing tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements, and...

Regulatory & Start Up Specialist Role OverviewThis position is responsible for participating in end-to-end site management from feasibility to site closure, serving as a primary point of contact for investigative sites and study team members.Key ResponsibilitiesSupport site qualification, regulatory green light, and site maintenance/close-outs.Participate in...

We are seeking a Regulatory Affairs Specialist to ensure the delivery of regulatory activities on a global level.Key ResponsibilitiesContribute to the production of client administrative documents for regulatory submissions.Compile regulatory dossiers in accordance with national requirements.Manage systems and administer regulatory processes.Track and...

We are seeking a Regulatory Affairs Specialist to contribute to ensuring the delivery of regulatory activities on a global level.Key Responsibilities:To assist in the production of client administrative documents for regulatory submissions.To compile regulatory dossiers in accordance with national requirements and ensure their accuracy.To manage systems and...

Job Description:We are looking for a skilled Regulatory Document Specialist to develop new projects that include managing and preparing regulatory applications in eCTD format. Key responsibilities include ensuring timely and accurate submissions, performing quality control, and maintaining knowledge of FDA, HC, and ICH requirements.Key...

Job DescriptionThis role ensures adherence to regulatory requirements, ensuring compliance with laws and regulations. Key responsibilities include maintaining documentation systems, record retention, and information services.About the RoleManage global regulatory submission projects, providing strategic input on technical-related regulatory strategy and...

EHS/HSE Content Manager and Regulatory SpecialistAt ERM, we're redefining the way organizations manage their environmental, health, and safety (EHS) regulatory requirements. We're looking for a skilled EHS/HSE Content Manager and Regulatory Specialist to join our team and help us achieve our mission. About the RoleThis is a senior-level position that...

Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at ProductLife Group. As a Regulatory Affairs Specialist, you will be responsible for managing post-approval activities for the Canadian market, including life cycle management, change controls, and regulatory submissions.Key Responsibilities:Manage...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, MEX Labcorp Clinical Development, S. de R.L. de C.V. provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than...

We are seeking a Quality Assurance Specialist to join our team at Freudenberg Group.**Job Summary:**This role is responsible for ensuring that our quality systems meet the required standards and that our products meet customer expectations.**Key Responsibilities:**• Evaluate and analyze quality data to identify trends and areas for improvement• Develop...

We are seeking a Regulatory Submission Specialist to join our team at ProductLife Group. The ideal candidate will have a strong background in regulatory affairs and experience with eCTD submissions.Key Responsibilities:Manage and prepare IND, NDA, BLA, and DMF regulatory applications in eCTD format for submission to the applicable regulatory authority...