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Regulatory Affairs Specialist

Lgcgroup · Milford, MA, United States · Hybrid · Active · $72,000–$97,000 / year · SmartRecruiters

Job facts

FieldValue
CompanyLgcgroup
TitleRegulatory Affairs Specialist
Normalized title-
Department / teamQuality Assurance and Regulatory Affairs
LocationMilford, MA, United States
Work modelHybrid / Hybrid
Employment typeFull Time
Salary$72,000–$97,000 / year
Statusactive
ATS providerSmartRecruiters
Posted / first seen2026-04-16 / 2026-05-31
Changed / last seen2026-05-31 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Lgcgroup.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through SmartRecruiters.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Milford.Open
Department jobsActive postings in Quality Assurance and Regulatory Affairs.Open
Work model jobsActive Hybrid postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyLgcgroup
Source83f5fcd4-e68b-481e-8dc8-eef103f08d97
ATS providerSmartRecruiters

Description

With 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. We'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 agencies Analyze and interpret regulatory requirements, mentorship materials, and industry standards to ensure organizational compliance Maintain comprehensive knowledge of current and emerging regulations affecting product development, manufacturing, and commercialization Develop and implement regulatory strategies for new product launches and existing product modifications Coordinate with quality assurance, research and development, and manufacturing teams to gather necessary information for regulatory submissions Monitor regulatory changes and communicate updates to relevant collaborators Maintain organized regulatory files and documentation systems in compliance with record-keeping requirements Conduct regulatory impact assessments and provide recommendations to senior management Support internal and external audits related to regulatory compliance Track regulatory timelines and ensure all submissions meet established deadlines Interact with regulatory agencies about submissions, inquiries, and compliance matters Minimum Qualifications: Minimum 3-5 years of experience in regulatory affairs, compliance, or quality assurance Bachelor's degree in a relevant field of study Strong knowledge of FDA regulations, Code of Federal Regulations (CFR), and Good Manufacturing Practices (GMP) Proficiency in preparing and managing regulatory submissions and documentation Excellent written and verbal communication skills with the ability to translate complex regulatory requirements into clear mentorship Advanced organizational and project management skills with the ability to prioritize several tasks simultaneously Proficiency with regulatory databases, electronic submission systems, and standard office software Strong analytical skills with the ability to interpret regulatory mentorship and industry standards Attention to detail and dedication to accuracy in all regulatory documentation Experience working cooperatively with diverse groups in a fast-paced environment Professional demeanor and ability to interact effectively with regulatory agencies and external partners Preferred Qualifications: Experience in the pharmaceutical, medical device, or healthcare industry Experience with global regulatory standards (European Union/IVDR, Canada, or other regions) Knowledge of quality assurance processes and procedures Experience with electronic submissions and digital regulatory systems Understanding of product lifecycle management from development through commercialization Advanced Excel skills and/or database experience The customary salary range for this position is: Minimum pay rate : $72,000 USD Maximum pay rate : $97,000 USD The 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: PASSION CURIOSITY INTEGRITY BRILLIANCE RESPECT Equal 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

Full job record

Job IDce3d6bcb4a2fbd479af0bfccc312b4e5c9f0143f
Org IDe2c2d32c-96b7-49c9-a6d3-d90dbdc4e28e
Source ID83f5fcd4-e68b-481e-8dc8-eef103f08d97
Board ID83f5fcd4-e68b-481e-8dc8-eef103f08d97
Providersmartrecruiters
Provider Job Key744000121274697
TitleRegulatory Affairs Specialist
Normalized Title
Statusactive
Activeyes
Location TextMilford, MA, United States
DepartmentQuality Assurance and Regulatory Affairs
Team
Employment Typefull_time
Workplace Typehybrid
Remote Policyhybrid
CountryUnited States
RegionMA
CityMilford
Salary RawUSD 72000-97000 year
Salary Min72,000
Salary Max97,000
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://jobs.smartrecruiters.com/LGCGroup/744000121274697-regulatory-affairs-specialist
Apply URLhttps://jobs.smartrecruiters.com/LGCGroup/744000121274697-regulatory-affairs-specialist?oga=true
First Seen At2026-05-31 17:42:28Z
Last Seen At2026-06-06 10:48:01Z
Last Checked At2026-06-06 10:48:01Z
Last Changed At2026-05-31 17:42:28Z
Inactive At
Source Posted At2026-04-16 18:41:08Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=smartrecruiters/board=lgcgroup/date=2026-06-06/2026-06-06T10-47-56-217Z-9625894523ee165344a3f1dadd7e3dff699b9185d60ebe0b7649cdbb5f80764d.json
Event Fields
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Parsed Structured
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Extensions
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Native Structured
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