Regulatory Affairs Specialist

Company DescriptionWith manufacturing sites across the US, UK, Germany and Denmark, LGC Biosearch Technologies has plans to continue growing. We deliver mission critical genomics to our diverse customer base in molecular diagnostics, pharma/biotech and agrigenomics. Our integrated portfolio of products, services and expertise supports our purpose of Science for a Safer World and we have embodied our mission by working with customers to enable research into life-altering treatment for disease and illness worldwide. We are currently seeking candidates who are up for the challenge of operating in a high-growth, purpose-driven organization.Job DescriptionWe're looking for a meticulous and analytical Regulatory Affairs Specialist to join our team in Milford, United States. This outstanding opportunity at LGC will allow you to be at the forefront of regulatory excellence and conformity, ensuring our organization competes successfully in the global marketplace. In this role, you will be responsible for ensuring our organization maintains full compliance with all applicable federal, state, and international regulatory requirements. The ideal candidate will demonstrate careful organizational skills, strong communication abilities, and a dedication to maintaining the highest standards of regulatory excellence. You will work collaboratively with cross-functional teams to navigate complex regulatory landscapes and drive timely product approvals.Prepare, review, and submit regulatory documentation and applications to the FDA and other regulatory agenciesAnalyze and interpret regulatory requirements, mentorship materials, and industry standards to ensure organizational complianceMaintain comprehensive knowledge of current and emerging regulations affecting product development, manufacturing, and commercializationDevelop and implement regulatory strategies for new product launches and existing product modificationsCoordinate with quality assurance, research and development, and manufacturing teams to gather necessary information for regulatory submissionsMonitor regulatory changes and communicate updates to relevant collaboratorsMaintain organized regulatory files and documentation systems in compliance with record-keeping requirementsConduct regulatory impact assessments and provide recommendations to senior managementSupport internal and external audits related to regulatory complianceTrack regulatory timelines and ensure all submissions meet established deadlinesInteract with regulatory agencies about submissions, inquiries, and compliance mattersQualificationsMinimum Qualifications: Minimum 3-5 years of experience in regulatory affairs, compliance, or quality assuranceBachelor's degree in a relevant field of studyStrong knowledge of FDA regulations, Code of Federal Regulations (CFR), and Good Manufacturing Practices (GMP)Proficiency in preparing and managing regulatory submissions and documentationExcellent written and verbal communication skills with the ability to translate complex regulatory requirements into clear mentorshipAdvanced organizational and project management skills with the ability to prioritize several tasks simultaneouslyProficiency with regulatory databases, electronic submission systems, and standard office softwareStrong analytical skills with the ability to interpret regulatory mentorship and industry standardsAttention to detail and dedication to accuracy in all regulatory documentationExperience working cooperatively with diverse groups in a fast-paced environmentProfessional demeanor and ability to interact effectively with regulatory agencies and external partnersPreferred Qualifications:Experience in the pharmaceutical, medical device, or healthcare industryExperience with global regulatory standards (European Union/IVDR, Canada, or other regions)Knowledge of quality assurance processes and proceduresExperience with electronic submissions and digital regulatory systemsUnderstanding of product lifecycle management from development through commercializationAdvanced Excel skills and/or database experienceAdditional InformationThe customary salary range for this position is:Minimum pay rate: $72,000 USDMaximum pay rate: $97,000 USDThe salary range provided covers the minimum and maximum amounts projected for this role. The base salary will be influenced by factors like experience, skills, and location.All your information will be kept confidential according to EEO guidelines.Join LGC and become part of a team that values collaboration, integrity, and brilliance in all we do. We are committed to encouraging a workplace where everyone can thrive and contribute to our mission.Our values:PASSIONCURIOSITYINTEGRITYBRILLIANCERESPECTEqual opportunities LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, parental responsibilities, religion, or belief. Shortlisting, interviewing, and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership.For more information about LGC, please visit our website www.lgcgroup.com#scienceforasaferworld