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Reproductive non clinical regulatory toxicologist

Maidstone
NonStop Consulting
Posted: 27 October
Offer description

Reproductive Toxicologist / Regulatory Toxicologist


I am supporting a global science-led organisation recognised for its long-standing commitment to product safety, regulatory excellence, and innovation. They are now seeking a Senior Regulatory Toxicologist to strengthen their global human health safety function, with a particular focus on developmental and reproductive toxicology.


This position offers the chance to apply deep scientific expertise in a business where data, risk evaluation, and innovation intersect. The role sits at the centre of regulatory decision-making, influencing how products are designed, tested, and brought to market responsibly across multiple regions.


Why This Role is Different

This is not a routine toxicology support role — it’s a strategic and visible position that shapes how safety and innovation coexist in a global setting. You’ll be the go-to expert for developmental and reproductive toxicology, supporting internal teams, regulators, and partners with scientifically sound assessments that underpin product approvals and ongoing compliance.


The company operates with a balance of scientific integrity and practical execution. You’ll work closely with regulatory affairs, product stewardship, and R&D to integrate toxicological thinking into every phase of product development — from early research to global launch. The work is diverse, combining complex data interpretation with proactive influence in regulatory and scientific discussions.


The organisation itself is known for its collaborative, knowledge-driven culture. It invests heavily in modern risk assessment methods — including the use of New Approach Methodologies (NAMs) and data analytics — while giving its experts autonomy to innovate and lead from the front.


Responsibilities

* Deliver high-level toxicological guidance to support global registration submissions, ensuring product safety positions are evidence-based and aligned with regulatory expectations.
* Act as the organisation’s recognised authority on developmental and reproductive toxicology (DART), providing scientific leadership on all matters related to human health risk assessment.
* Plan and manage toxicology programmes, commissioning and supervising studies conducted against REACH and/or TSCA
* Company representation at trade association / body meetings as well as mentor staff providing strategic direction.


Key Requirements

* PhD or equivalent degree in Toxicology, Biology, Biochemistry, or related field
* 10–15 years’ experience in regulatory toxicology and proven reproductive developmental toxicology expertise
* Demonstrated ability to evaluate toxicological data within global regulatory frameworks
* Experience supporting global chemical or product registrations under REACH, TSCA, or equivalent schemes
* Certified or eligible for ERT (European Registered Toxicologist)
* Fluent English (additional European languages beneficial)


For more information, send your CV to this advert or email Abid Kanji on a.kanji@nonstopconsulting.com

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