Regulatory Affairs Specialist at LGC Group

Milford, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

16 Jul, 26

Salary

97000.0

Posted On

17 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory affairs, Compliance, Quality assurance, FDA regulations, Code of federal regulations, Good manufacturing practices, Regulatory submissions, Project management, Regulatory strategy, Technical writing, Communication, Analytical skills, Documentation, Risk assessment, Audit support, Product lifecycle management

Industry

Biotechnology Research

Description

Company 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. Job Description 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 Qualifications 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 Additional Information 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 Work Arrangement: Hybrid Department: Quality Assurance and Regulatory Affairs Compensation: USD 72000 - USD 97000 - yearly

Responsibilities

The Regulatory Affairs Specialist is responsible for ensuring organizational compliance with federal, state, and international regulatory requirements. They will prepare and submit regulatory documentation while collaborating with cross-functional teams to drive product approvals.