Regulatory Affairs Specialist

hace 1 mes


Santiago de Querétaro, Querétaro de Arteaga, México Kerry A tiempo completo
Job Title: Regulatory Specialist

At Kerry, we are seeking a highly skilled Regulatory Specialist to join our team. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with relevant regulations and standards.

Key Responsibilities:
  • Implement changes to standard documentation based on new regulations as needed.
  • Develop a regional network of experts to support and develop knowledge.
  • Participate in Kerry's Regulatory Affairs Steering Group.
  • Work as a customer champion to ensure documentation turnaround time consistently meets or beats customer segmentation and service level agreements.
  • Act as the regulatory liaison to account managers, customer care for standard documentation requests, recipe change management, vendor documentation collection, and other duties as assigned.
  • Execute against functional initiatives.
  • Work in partnership with regulatory team members and other Kerry colleagues.
  • Support internal/external stakeholders by providing standardized technical information, including site quality technical packets and customer questionnaires.
  • Create and maintain regulatory documents.
  • Manage emerging issues, including being the point of contact to internal stakeholders to solve customer issues as required.
  • Understand and share best practice/trends internally, including knowledge management across regions.
  • Perform various duties assigned from manager, including queries, projects, audit support.
  • Routine metrics reporting to the business and attendance at business meetings as required.
  • Lead regulatory-related business projects as appropriate.
  • Develop relationships with customer contacts to facilitate continued/improved business relationships.
  • Process recipe changes (ECORs, Kerry Tracks), requests for information for sample delivery, collect vendor documentation for raw materials.
Qualifications and Skills:
  • Full understanding of relevant regulations globally.
  • Key technical contact for identified customers, with responsibility to foster good relationships.
  • Understanding of the Food Industry structure and regulatory implications.
  • Food regulatory and legislative knowledge.
  • Capability to train and support junior members of the department/RDA function as appropriate.
  • Ability to identify opportunities for the regulatory function to enable business growth.
Language Requirements:
  • Fluent in English.
Technical Competencies:
  • Computer literate with a working knowledge of Microsoft Office.
  • Experience in SAP and Optiva systems an advantage.
  • Fluency in English. Fluency in another language an added advantage.
Qualifications and Skills:
  • 5+ years post-grad in food/pharma regulatory or quality industry.
  • Food industry knowledge.
  • Executes using established processes and structures.
  • Analytical, self-starter, decisive, and able to perform under pressure and a team player; able to take instruction and perform work accordingly.
  • Possess good co-operation/communication/presentation/interpersonal and organization skills.
  • Excellent communication skills.


  • Santiago de Querétaro, Querétaro de Arteaga, México Kerry A tiempo completo

    Key ResponsibilitiesAs a Regulatory Specialist at Kerry, you will be responsible for implementing changes to standard documentation based on new regulations as needed. You will develop a regional network of experts to support and develop knowledge, actively participate in Kerry's Regulatory Affairs Steering Group, and work as a customer champion to ensure...


  • Santiago de Querétaro, Querétaro de Arteaga, México Kerry A tiempo completo

    Job Summary:Kerry is seeking a highly skilled Regulatory Affairs Specialist to join our team.Key Responsibilities:Implement changes to standard documentation based on new regulations as needed.Develop a regional network of experts to support and develop knowledge.Actively participate in Kerry's Regulatory Affairs Steering Group.Work as a customer champion to...


  • Ciudad de México, Ciudad de México ProductLife Group A tiempo completo

    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...


  • Ciudad de México, Ciudad de México Thermo Fisher Scientific A tiempo completo

    In this role as a Regulatory Affairs Specialist, you will be part of our Regulatory Liaison team, leading on communications with regulatory agencies as part of centralized regulatory submissions. You will partner with our Regulatory Affairs leads, in providing regulatory affairs strategy and technical/project leadership on a regional/global level.Key...


  • Ciudad de México, Ciudad de México ProductLife Group A tiempo completo

    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...


  • Ciudad de México, Ciudad de México ProductLife Group A tiempo completo

    Job DescriptionWe are seeking a highly skilled Global Regulatory Affairs Specialist to ensure the delivery of regulatory activities on a global level. This role requires strong organizational and interpersonal skills, with excellent oral and written communication abilities.


  • Ciudad de México, Ciudad de México ProductLife Group A tiempo completo

    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...


  • Ciudad de México, Ciudad de México ProductLife Group A tiempo completo

    In the context of a new project, we are seeking a Regulatory Affairs Specialist to support our teams in Mexico/LATAM.Key ResponsibilitiesProvide guidance and support on Mexican and Central America legislation.Contribute to regulatory activities, including pre-licensing, new registrations, and post-licensing submissions.Assist in the production of client...


  • Ciudad de México, Ciudad de México Solventum A tiempo completo

    Job Description:Regulatory Affairs Specialist, Mexico (Solventum)Solventum is a company committed to innovation and excellence in the healthcare sector. We are seeking a highly skilled Regulatory Affairs Specialist to join our team in Mexico.Key Responsibilities:Provide regulatory support for medical products sold in Mexico, including managing licenses with...


  • Ciudad de México, Ciudad de México Novo Nordisk AS A tiempo completo

    Position for Novo Nordisk GBS MexicoPursue a challenging career in regulatory affairs with Novo Nordisk's Global Business Service Centre in Mexico City.We are seeking a highly skilled Regulatory Affairs Coordinator to support the compilation, submission, and approval of Country Specific Submissions files for responsible countries.Key ResponsibilitiesSupport...


  • Ciudad de México, Ciudad de México ProductLife Group A tiempo completo

    Job TitleRegulatory Affairs Specialist in CanadaAbout UsProductLife Group is a leading provider of regulatory services for the pharmaceutical industry.Job DescriptionWe are seeking an experienced Regulatory Affairs Specialist to join our team in Mexico or Canada. As a Regulatory Affairs Specialist, you will be responsible for managing post-approval...


  • Ciudad de México, Ciudad de México Solventum A tiempo completo

    Job OverviewSolventum is seeking a highly skilled Regulatory Affairs Specialist to join our team in Mexico. As a Regulatory Affairs Specialist, you will be responsible for providing general regulatory support for medical products sold in Mexico, including managing medical product licenses with COFEPRIS, reviewing and approving product labeling and...


  • Ciudad de México, Ciudad de México Solventum A tiempo completo

    Improve Healthcare with SolventumSolventum is a company dedicated to enhancing healthcare by pioneering game-changing innovations at the intersection of health, material, and data science. As a Regulatory Affairs Specialist, you will be part of our team that ensures every solution created for our customers' toughest challenges adheres to the highest...


  • Ciudad de México, Ciudad de México Icon Plc A tiempo completo

    The Regulatory Affairs Specialist will contribute to the preparation, compilation, and submission of regulatory documents, including CT/IND, MAA, and NOA. Key Responsibilities:- Regulatory Document Preparation: Prepare and submit regulatory documents in a timely and accurate manner.- Collaboration with Teams: Work with the Regulatory Submissions team and...


  • Ciudad de México, Ciudad de México Thermo Fisher Scientific A tiempo completo

    In a pivotal role at Thermo Fisher Scientific, the Sr Regulatory Affairs Specialist will be part of our Regulatory Liaison team, spearheading communications with regulatory agencies as part of centralized regulatory submissions. This includes collaboration with regulatory affairs leads to provide strategic guidance and technical/project leadership on a...


  • Ciudad de México, Ciudad de México Mccormick & Company A tiempo completo

    **Scientific and Regulatory Affairs Manager LATAM**Mccormick & Company, a world leader in the spice, flavor and seasonings industry, is seeking a full time Scientific and Regulatory Affairs Manager LATAM. This new hire will work in our Mexico City location.We create differentiating flavors consumers prefer with unmatched quality, science, innovation and...


  • Ciudad de México, Ciudad de México Qiagen A tiempo completo

    Regulatory Affairs Manager RoleWe are seeking an experienced Regulatory Affairs Manager to lead and undertake regulatory responsibility for Mexico and Central Americas to ensure our IVD products comply with regional regulations and laws.This role involves developing and implementing regulatory strategies to facilitate product approvals, registrations, and...


  • Ciudad de México, Ciudad de México Novo Nordisk AS A tiempo completo

    Position OverviewWe are seeking a Regulatory Affairs Coordinator to join our team in GBS Mexico City. As a key member of our Global Business Service team, you will be responsible for supporting the compilation, submission, and approval of Country Specific Submissions files.About the RoleAs a Regulatory Affairs Coordinator at Novo Nordisk A/S, your main...


  • Ciudad de México, Ciudad de México ICON Plc A tiempo completo

    Regulatory Affairs Specialist with Expertise in Clinical TrialsAt ICON Plc, we're seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs team, you will be responsible for leading the preparation, submission, and maintenance of regulatory documents for clinical trials. Your expertise in clinical...


  • Ciudad de México, Ciudad de México Ortho Clinical Diagnostics A tiempo completo

    The OpportunityAt Ortho Clinical Diagnostics, we are committed to delivering innovative solutions that transform the power of diagnostics into a healthier future for all. We are seeking a highly skilled Regulatory Affairs Associate to join our team and contribute to our mission.Key ResponsibilitiesPrepare and submit regulatory documents, including technical...