Senior Regulatory Affairs Specialist

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🕒 April 28

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CDM Smith

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1947

⚡ Energy

Engineering • Construction • Environment • Infrastructure • Energy

CDM Smith is a privately owned engineering and construction firm that provides expert consulting and smart solutions in the sectors of water, environment, transportation, energy, and facilities. The company is committed to addressing and solving the world's environmental and infrastructure challenges through innovation and sustainable practices. CDM Smith works with public clients, industry investors, and offers development assistance to drive transformative projects worldwide. Their mission is to make the world better, safer, and more resilient, while fostering a secure and attractive workplace for their employees.

📋 Description

• Lead regulatory strategy and execution for assigned Professional Hygiene and Crop Protection products across EMEA in compliance with relevant regulations (PPP, BPR, REACH, CLP, and national requirements). • Act as Regulatory Lead for assigned active substances, owning dossiers and overseeing technical content, submission planning, and procedural compliance with EU authorities (e.g. RMS, co‑RMS, EFSA). • Coordinate and deliver EMEA product registration activities, including compilation, submission, and lifecycle management of regulatory dossiers (PPP, BPR, national transitional). • Manage post‑submission activities and interact with regulatory authorities, task forces, and external stakeholders to achieve positive regulatory outcomes. • Provide clear regulatory analysis, guidance, and recommendations to internal stakeholders and customers to support strategic and commercial decisions. • Collaborate closely with R&D, Toxicology, and Hazard Communication teams on scientific and technical aspects of regulatory projects. • Coordinate with consultants and data providers as needed. • Monitor evolving regulatory requirements and proactively assess and communicate potential impacts on the product portfolio.

🎯 Requirements

• Master’s degree in natural sciences or a related discipline (PhD is an advantage). • Typically 5–10 years of experience in Regulatory Affairs within the chemical, biocides, or crop protection industry. • Strong working knowledge of the EU regulatory framework for plant protection products and biocides (PT1–5), with exposure to REACH and CLP. • Experience with EU Active Substance registration under Regulation (EC) No 1107/2009 is highly desirable. • Solid scientific understanding of areas such as chemistry, toxicology, ecotoxicology, efficacy, or risk assessment. • Business‑fluent English with strong written and verbal communication skills. • Proactive, resilient, and detail‑oriented, with the ability to manage multiple priorities and work effectively under pressure in a matrix organization.

🏖️ Benefits

• Equal opportunity employer