BAT is evolving at pace - truly like no other organisation.
To achieve the ambition, we have set for ourselves, we are looking for colleagues who are ready to live our ethos every day. Come be a part of this journey!
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BAT UK IS LOOKING FOR AN IN VITRO LABORATORY TOXICOLOGIST
SENIORITY LEVEL: Experienced Non-Management Level
FUNCTION: Scientific Research
SUB FUNCTION: Scientific Research
LOCATION: Southampton, UK
TYPE OF CONTRACT: Permanent
BENEFITS
- UK yearly Incentive Bonus – competitive % based on business results and average annual salary
- Attractive Private Pension Plan - up to 15%, Private Medical cover, Doctor @hand-24/7 GP appointments, by video or by phone, 365 days a year, from anywhere in the world
- Share Reward Scheme (free shares and share saving scheme), Group Personal Accident Insurance, Life Assurance
- Flexible Benefits Scheme: Tax Return Assistance, Cycle To Work, Holiday Trading, Dental Insurance, Travel Insurance; Onsite Gym and Gyms Discounts-discounts at over 3,700 gyms, SPAs, pools, studios and outdoor fitness events across the UK; Season Ticket loans-Interest free loans for purchase of annual tickets for public transport
What are the key objectives and expectations from this role?
Support the execution of pre-clinical capabilities, inclusive of in silico and in vitro toxicology studies, for predominantly regulatory submissions, inclusive of but not limited to FDA authorisations and approvals.
The role will be responsible for supporting the tools, knowledge, and data in preclinical sciences across all BAT categories.
The primary purpose for of preclinical data is to satisfy BAT’s duty of care by substantiating consumer product safety, meeting regulatory obligations and providing scientific substantiation of health-related claims such as reduced risk versus a cigarette or wellbeing and stimulations claims in the beyond nicotine strategy.
The role will also partner with the team accountable for bringing new preclinical capabilities into BAT, including Science Discovery function, to ensure we can meet our emerging needs such as disease focussed toxicity mechanisms.
The scientific programme must position BAT, and any associated acquisitions or investments, product portfolio as a trusted brand in safety and efficacy and must be recognised credibly externally.
What is the direct impact of this role on the team or organization?
The pre-clinical screening and evaluation capabilities will be utilised in supporting BATs nicotine and tobacco and beyond tobacco product category strategy, in the first instance enabling launches and in the second instance identifying a competitive pipeline.
Role directly delivers BAT’s core purpose of A Better Tomorrow, via the science and technical framework proving the reduction in public health impact of our business
Reports to
Senior Scientist Pre Clinical Regulatory
Number of Direct Reports
0
Core Relationships
Internal - Scientific Research, New Categories R&D, Procurement, US Submissions Teams
External - Regulators, 3rd Party suppliers
Geographic Scope
Global
Travel Required
Infrequent
WHAT YOU WILL BE ACCOUNTABLE FOR
- Support the execution of the delivery of the data packages to submit regulatory dossiers, such as the FDA pre-market approvals and modified risk claims
- Lead the maintenance and running of the relevant laboratory requirements to support the pre-clinical team
- Input into applying knowledge in a broad range of cell biology and in-vitro toxicology methodologies, including knowledge of respiratory and / or cardiovascular diseases
- Input in the delivery of high content screening approaches, data integration and analysis to support pre-clinical and consumer product safety assessments for regulatory purposes
- Input into engagement activities with key stakeholders and prepare and deliver presentations at internal and external meetings on behalf of BAT Scientific Research
- Identify requirements and approve procedures/processes to ensure ‘Best Practice’ is followed e.g. HTA; GLP.
- Input in the development of pre-clinical assessment strategies to deliver transformational skills and cutting-edge capabilities for product assessment.
- Monitor the competitor landscape and coordinate the activities of preclinical researchers, statisticians, data analysts and other research team members involved in pre-clinical studies.
- Contribute to regulatory dossier preparations, internal and external communications, and publications.
- Complete tasks in accordance with BAT R&D business strategy and the code of business conduct.
CAN THIS BE YOUR FUTURE ROLE?
- Have you performed in vitro toxicology studies?
- Do you have experience in high throughput assays?
- Have you experience in genetic toxicology assays?
ESSENTIAL EXPERIENCE, SKILLS, AND KNOWLEDGE
Experience Required
- Expertise in cell biology, molecular toxicology, or pharmacology with a relevant degree and preferably PhD in biological sciences.
- Proven ability in the application of innovative in-vitro approaches in the pre-clinical field to bridge to clinical endpoints and human health effects.
- Preferably, experience in disease pathways/ adverse outcome pathway-based approaches
- Demonstrable ability to apply bioinformatics tools to process and assess biological data.
- Demonstrable experience in disease modelling, adverse outcome pathways, toxicology and / or pharmacology with the ability to set the strategy for the team - integrating and interpreting complex data to provide clear guidance and support for product launches and the evaluation of the competitor and safety landscape.
- Ability to apply knowledge in a broad range of novel in-vitro biology / toxicology methodologies to determine direction.
- Expertise in basic IT (Word/ Excel/ Power Point) and the application of bioinformatics, data analysis / computational tools.
Technical / Functional / Leadership Skills Required
- Proven track record in execution of in vitro studies
- Study design and interpretation in a relevant field
- Proven skills at scientific communication to technical and non-technical, internal, and external audiences
Education / Qualifications / Certifications Required
- Relevant degree in biological sciences
BENEFICIAL
- Experience in FDA submissions and engagement
- PHD in biological sciences
WE ARE BAT
At BAT we are committed to our Purpose of creating A Better Tomorrow. This is what drives our people and our passion for innovation. See what is possible for you at BAT.
- Global Top Employer with 53,000 BAT people across more than 180 markets
- Brands sold in over 200 markets, made in 44 factories in 42 countries
- Newly established Tech Hubs building world-class capabilities for innovation in 4 strategic locations
- Diversity leader in the Financial Times and International Women’s Day Best Practice winner
- Seal Award winner – one of 50 most sustainable companies
BELONGING, ACHIEVING, TOGETHER
Collaboration, diversity and teamwork underpin everything we do here at BAT. We know that collaborating with colleagues from different backgrounds is what makes us stronger and best prepared to meet our business goals. Come bring your difference!
