Conventional Safety Specialist Job at AWE (Aldermaston near Reading)

Nuclear Safety Assessment Specialist

Our Nuclear Safety Team makes sure that we keep our operations running as they s...

Location

United Kingdom , Aldermaston near Reading

Salary:

23500.00 GBP / Year

AWE

Expiration Date

Until further notice

Requirements

Any Engineering or Science based degree
Growth mindset
Curiosity
Innovation
Resilience
Teamwork

Job Responsibility

Work across the full project lifecycle, from designing new facilities to upgrading existing ones
Support research and production and help to safely decommission old sites
Solve complex technical problems
Model accident scenarios
Write detailed reports on how we manage nuclear, radiological, environmental and conventional risks
Collaborate with a range of experts including engineers, operators, project managers and external regulators
Build strong connections while delivering on real-time projects
Support the analysis of nuclear radiological, chemical, explosives and other major hazards associated with facilities, plant, equipment and products
Break down complex risks
Help design safety cases

What we offer

270 hours of annual leave
Nine-day fortnight (every other Friday off)

Fulltime

Senior Physician, Patient Safety

Join our dynamic Patient Safety team as a Senior Physician where you'll leverage...

Location

United States; Canada , Remote; Alberta

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experience in clinical medicine (general or specialist qualifications) which is expected to be kept up to date
Good knowledge of drug safety and the drug development process
Good knowledge/understanding of medical terminology
Relevant experience in pharmacovigilance/ Drug Safety/ Clinical Practice
3 - 5 years previous experience in pharmacovigilance and/or medical monitoring is required
US Board Certification/board eligibility or regional equivalent for Canada
Bachelor of Medicine, Bachelor of Surgery (MBBS) / Doctor of Medicine (MD)/ Medically qualified from an acknowledged Medical School
Completion of at least basic training in clinical medicine (residency, internship etc.)
Demonstrated success in technical proficiency and scientific creativity
Good presentation and verbal/written communication skills

Job Responsibility

Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and global drug safety regulations and guidelines
Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting
Performing medical review of cases not limited to (including complex and challenging cases requiring expert judgement)), clinical trial, and literature cases including combination products {drug-device}) according to client/Parexel Standard Operating Procedures (SOPs
as applicable) and liaising with the client, as require
Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality
Review appropriateness of medical content in narrative for medical coherence
Assessing seriousness, listedness / expectedness of reported events
Providing medical inputs to case processing team
Raising appropriate follow-up queries for relevant information from the reporter/HCP (Health Care Professional)
Review and verify appropriate selection of adverse events from source documents, assign appropriate Medical Dictionary for Regulatory Activities (MedDRA) code, review narrative

What we offer

Flexible approach to work that meets your personal needs
Work from home
Benefits vary by country
Investment in your professional and personal development

New

Therapeutic Specialist - Diabetes

Therapeutic Specialist, Tzield are part of the National Tzield Sales Team and pl...

Location

United States , Long Island, NY

Salary:

125250.00 - 208750.00 USD / Year

Sanofi

Expiration Date

Until further notice

Requirements

B.A. / B.S. degree required
3+ years of pharmaceutical, biotech or medical device sales experience
Account Management sales and / or rare specialty product experience
Demonstrated ability to understand and use data to drive improved business management and oversight of the sales within customer territories
Proven results of increasing educational awareness, provider adoption and customer engagement
Experience successfully launching products in the field
Experience collaborating and working in a matrix environment across multiple different sales, medical and support functions
Strong business acumen and solution-oriented mind-set
Ability to strategically plan and execute work
Robust communication skills and ability to engage in two-way stakeholder dialogue

Job Responsibility

Brand Awareness & Intent to Treat with Endos Build belief in Tzield mechanistic rationale and clinical narrative (e.g., MOA involving beta cell preservation, approved indication, efficacy / safety profile)
Develop in-depth knowledge and understanding of key accounts across territory, including barriers to Tzield use
Contribute to priority account strategy development lead by SAMs and own execution to engage endocrinology and primary care providers on Tzield use
For non-priority Endo in territories, own the development and execution of growth-oriented account & business plans (e.g., account mapping, influence mapping, etc.)
Identify account champions / KOLs and engage them as necessary and appropriate to communicate with peers and patients about Tzield
Screening Awareness & Development of T1D Ecosystem Build belief in T1D early detection and importance of screening for T1D in asymptomatic, undiagnosed, early detection population
Conduct strategic planning at territory level to understand and contribute to development of broader T1D ecosystem in order to prioritize time, engagement, and education strategy
Contribute to screening strategy development and own execution to engage PCP / Ped on early detection & screening
Collaborate with stakeholders to identify and educate on importance of urgent referrals for identified patients within narrow treatment window
Educate relevant stakeholders on at-risk populations, screening / monitoring best practices, and the value of early detection (e.g., DKA avoidance)

What we offer

High-quality healthcare
prevention and wellness programs
at least 14 weeks’ gender-neutral parental leave

Fulltime

Technical Specialist I – W&C Applications

This individual is independent for basic support needs and is learning from othe...

Location

United States

Salary:

71000.00 - 91000.00 USD / Year

H.B. Fuller

Expiration Date

Until further notice

Requirements

High School Diploma and at least 5 years of relevant work experience
Associate or technical degree in a related area and at least 2 years of relevant work experience
Bachelor of Science degree in Chemistry, Chemical Engineering, or related field

Job Responsibility

Proactively maintain a safe work environment by following company guidelines, industry safety rules, and using proper protective equipment
Build strong relationships with customers, influence decisions, and gain alignment
Apply application and equipment expertise to solve unmet customer needs, troubleshoot process problems, support claim investigations, and recommend products or process improvements based on data-driven conclusions
Train and educate customers on H.B. Fuller products and services, including product specifications, application, and equipment
Conduct manufacturing audits at customer locations, where applicable
Perform preventative maintenance and equipment repair of H.B. Fuller-manufactured equipment, where applicable
Utilize equipment and application expertise to construct new apparatus or modify existing equipment based on customer and equipment capabilities
Develop expertise in H.B. Fuller products and applications in the markets served
Stay current with industry trends by attending conventions, trade shows, and visiting key equipment manufacturers, machinery partners, institutes, and substrate suppliers
Maintain knowledge of customers, competition, market forces, and product/application needs

What we offer

comprehensive benefits
incentive and recognitions programs
health & wellness benefits
401K contributions
paid time off
paid holidays

Fulltime

New

Cadd Specialist

This role will provide technical drawing and CAD support services to internal an...

Location

United States , San Antonio

Salary:

70000.00 - 85000.00 USD / Year

Bodwé Professional Services

Expiration Date

Until further notice

Requirements

Associate’s degree in computer-aided design and drafting (CADD) from an accredited institution, or a CADD certificate from an accredited technical or vocational school
Minimum of two (2) years of documented experience using Autodesk AutoCAD or equivalent CAD software to create, modify, and maintain engineering or architectural drawings
Ability to read and interpret construction and as-built drawings for architectural, mechanical, and infrastructure systems
Must have or be able to obtain and maintain a Real ID or Passport in order to undergo commercial airfare travel
Must have or be able to obtain and maintain a valid driver's license

Job Responsibility

Update architectural and infrastructure as-built drawings to reflect additions, relocations, and modifications
Validate project room information changes in compliance with Medical Health Systems Space Planning Criteria
Update the DMLSS/LogiCole system with required room and facility information per DHA-FE standard operating procedures and project policies
Upload and link drawing elements to the DMLSS/LogiCole system
Perform all drawing work using current versions of Autodesk AutoCAD, Revit, or equivalent CAD software in accordance with DHA policies, procedures, and AEC standards
Assist MTF facility managers in organizing, maintaining, and updating building drawings, plans, and master plans
Follow DHA-defined file naming conventions and technical standards for drawing file management
Upload and maintain 100% Issued For Construction (IFC) design documents and red-lined As-Built or final Record Drawings in the MARS database
Produce Record Drawings by updating 100% IFC files with red-lined As-Built submissions if not provided by the construction contractor
Perform remote updates using phone, web conference, email, or fax for changes affecting less than 5,000 square feet within a single contiguous building

Fulltime

New

Medical Science Liaison

GSK is looking to hire a Medical Science Liaison, HIV to join our ViiV Healthcar...

Location

Canada , Mississauga; GTA

Salary:

115000.00 - 165000.00 CAD / Year

GSK

Expiration Date

Until further notice

Requirements

Advanced post-graduate scientific degree (MD, PhD, or PharmD)
Strong ability to interpret and communicate scientific and medical data in peer-to-peer discussions
Exceptional presentation and public speaking skills
Excellent interpersonal and collaboration skills with a focus on teamwork and execution
Knowledge of regulations governing medical information exchange in the Canadian pharmaceutical environment
Strong negotiation, leadership, and organizational skills
Valid driver’s license
Ability to work independently in a field-based role with significant travel (up to 70%)

Job Responsibility

Build and maintain strong peer-to-peer scientific relationships with key HIV external experts
Present balanced and credible scientific data and support medical education initiatives
Serve as a scientific expert in virology, maintaining deep knowledge of HIV disease, treatments, and the competitive landscape
Respond to unsolicited medical inquiries with accurate, non-promotional information
Engage with a wide range of stakeholders including healthcare professionals, investigators, advocacy groups, and formulary decision-makers
Act as a key liaison between the external healthcare community and internal ViiV teams, gathering insights to inform strategy
Provide scientific support at regional, national, and international medical conferences
Deliver scientific training to sales teams using approved materials
Collaborate with clinical development teams to identify and support clinical trial sites
Travel up to 70% within the assigned territory

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

New

Senior Technical Program Manager

We are seeking a Senior Technical Program Manager to drive execution, alignment,...

Location

United States , New York

Salary:

165000.00 - 200000.00 USD / Year

Genius Sports

Expiration Date

Until further notice

Requirements

6+ years of experience in technical program management
Demonstrated ability to coordinate delivery across multiple engineering teams and long-running initiatives
Comfort engaging deeply with technical discussions to understand requirements, constraints, and delivery risk
Excellent written communication skills, with experience authoring well scoped tickets for engineers and progress updates for stakeholders
Strong understanding of cloud infrastructure, DevOps practices, and distributed systems
Experience working with SRE or on-call operations models
Hands-on familiarity with: Container orchestration (e.g., Kubernetes)
Infrastructure as Code and CI/CD pipelines
Observability and operational tooling
AWS services (e.g., EC2, EKS, CloudWatch, IAM) or equivalent cloud platforms

Job Responsibility

Drive execution of cross-functional programs spanning multiple platform and product teams
Translate high-level initiatives into structured program plans with clear scope and milestones
Establish and run program operating rhythms, including planning, execution tracking, reviews, and retrospectives
Identify, track, and manage dependencies and risks across teams with competing priorities
Partner with technical leads to ensure initiatives balance developer velocity, operational excellence, security, and cost efficiency
Support initiatives such as multi-region Kubernetes platforms, MLOps workflows, standardized deployment systems, and shared authentication services

What we offer

Eligible to take part in Genius Sports Group's benefits plan
Competitive salary and range of benefits
Committed to supporting employee wellbeing and helping you grow your skills, experience and career

Fulltime

New

Knowledge Management Analyst

We are looking for a Knowledge Management Analyst to help develop and maintain a...

Location

Estonia , Tallinn

Salary:

Not provided

Genius Sports

Expiration Date

Until further notice

Requirements

Experience working with knowledge management, training or LMS programs
Strong written and spoken English skills
Experience using data visualization tools and creating educational content such as tutorials or guides
Ability to communicate complex information clearly to audiences with different skills
Strong prioritization, organization, and time management skills
Excellent communication and interpersonal skills
Experience managing projects and presenting information to stakeholders

Job Responsibility

Maintain accurate, high-quality, and searchable knowledge base content for both internal and external users
Connect teams across Operations to ensure the right knowledge and resources are shared
Track knowledge base usage and measure the impact and efficiency of documentation and learning materials
Coach and promote knowledge sharing practices across the Service area
Plan, test, and implement tools and processes that improve how knowledge is created and maintained
Create and manage structured documentation such as guides, FAQs, and training materials
Support continuous improvement by identifying outdated content, improving knowledge workflows and constantly seeking for better solutions

Conventional Safety Specialist

AWE

Location:
United Kingdom , Aldermaston near Reading

Category:
Public Sector

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 23, 2025

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Location:United Kingdom , Aldermaston near Reading

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Job Description:

Job Responsibility:

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