Senior Consultant (m/f/d) Chemical Regulatory Affairs

at  Rambll

London SE1, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate25 Jul, 2024Not Specified01 May, 2024N/AGood communication skillsNoNo
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Description:

COMPANY DESCRIPTION

We invite you to bring your experience of product safety and stewardship into play as you support organisations around the world bring to the market products in a range of uses that meet relevant regulatory requirements and are safe for human health and the environment.
o succeed in this role, you must have a strong academic background in chemistry, toxicology, ecotoxicology, sustainability, or a similar subject, and possess several years of experience in product stewardship, chemical compliance and / or regulatory affairs. Are you our Senior Regulatory Affairs Consultant? Click the apply-button to send your application.

Responsibilities:

Your key tasks and responsibilities will be:

  • Providing subject matter expertise in chemical legislation (e.g., UK REACH, EU REACH, CLP, etc.) for the team
  • Providing authorisation strategies and regulatory advice for clients (including development of testing programmes for industrial chemicals)
  • Compiling approval/authorisation dossiers according to the EU and GB Chemical Regulations (e.g., REACH, Biocide)
  • Performing hazard, exposure and risk assessment, and/or efficacy assessments, in your field of expertise
  • Coordinating collaborative and timely preparation of application dossiers for the chemical industry together with our subject matter experts
  • Communication and close cooperation with our clients and the competent authorities
  • Supporting project management and existing client relationships
  • Develop and maintain a comprehensive understanding of the current and future regulatory landscape, attending conferences to keeping up to date with developments in the appropriate laws and guidance
  • Provide support to business development activities by providing industry expertise when needed during visits to clients, through discussion and responses to new project briefs and administratio

From the moment you join Ramboll, we will support your personal and professional development so that you grow with the company. For this role, we believe your starting point is:

  • Strong academic background with, as a minimum, a relevant science-based degree
  • You may also have a further degree in a relevant subject and/or relevant professional experience or qualifications (e.g., toxicology)
  • Prior experience of, or evidence of working in product regulatory affairs and product stewardship
  • Knowledge and understanding of regulatory affairs, especially European regulations governing product safety and stewardship, ideally with demonstratable experience as a regulatory specialist in industry or consultancy
  • Knowledge of EU and GB chemical regulatory requirements and/or global regulatory requirements an advantage
  • Strong skills in project management
  • Experience with IUCLID 6 and human or environmental exposure models (e.g., Chesar, EUSES)
  • IT packages including MS Word, MS Excel and MS Outlook.
  • Fluent in English, but other languages may be an asse


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

London SE1, United Kingdom