100 Safety Team jobs in Ireland
Food Safety Officer
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Health & Safety Officer
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Health & Safety Officer
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Health & Safety Specialist Limerick
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Functional Safety Manager

Posted 4 days ago
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Cadence is a pivotal leader in electronic design, building upon more than 30 years of computational software expertise. The company applies its underlying Intelligent System Design strategy to deliver software, hardware and IP that turn design concepts into reality.
Cadence customers are the world's most innovative companies, delivering extraordinary electronic products from chips to boards to systems for the most dynamic market applications including consumer, hyperscale computing, 5G communications, automotive, aerospace industrial and health.
At Cadence, we hire and develop leaders and innovators who want to make an impact on the world of technology.
Job Title: Design Engineering Director
Location: Edinburgh
Reports to: Sr Solutions Architect
Job Overview:
The Functional Safety Manager will be responsible for the ISO 26262 safety management of Cadence design IP products targeted for automotive products, and development of ISO 26262 compliant processes, infrastructure, and work products. He/she will work with the safety organizations of our customers, vendors, external safety expert consultants and internal product development teams to ensure that the functional safety process is well understood, executed and documented.
This role will be an integral part of an agile engineering team that focuses on bringing safety solutions per the ISO26262 standard to Cadence customers in the fast growing Automotive/ADAS markets.
This individual will support the organization's mission, vision, and values by exhibiting the following behaviors: excellence and competence, collaboration, flexibility, innovation, respect, accountability, ownership, and a sense of humor.
Job Responsibilities:
+ Act as Functional Safety Manager for safety related hardware and software products
+ Analyze impact of ISO 26262 releases for DIP and create Functional Safety awareness across department
+ Perform safety management activities according to relevant standards during all project phases (concept, product development, production) such as developing safety plans including defining the necessary safety related activities, work products and processes
+ Manage creation of safety work products which include the Safety Plan, Safety Manual, Safety Requirements, and Safety Analysis including FMEDA and DFA and Safety Verification and Validation activities
+ Collaborate with project engineers, marketing & development team, safety consultants, vendors and customers on Functional Safety activities
+ Define and implement functional safety processes associated with hardware development
+ Create/review functional safety documentation according to ISO 26262
+ Conduct reviews with product teams to ensure functional safety standards are being met throughout product development cycles
Job Qualifications:
+ BSEE/BS Computer Science, Computer Engineering, Electrical Engineering (or equivalent). MS preferred.
+ 10+ or more years of relevant work experience.
+ Experience with ISO 26262 standard. Preferable if holds Safety certification.
+ Experience in functional safety compliance, testing or auditing or QA (quality assurance) of embedded HW/SW systems
+ Experience in safety analysis of hardware including FMEA, FMEDA and DFA
+ Experience in working with certification bodies to gain product certification to ISO26262
+ Experience with standards-based embedded HW/SW systems Product Development Life Cycle i.e. HW IP design and verification processes, ASIC design methodologies, and software development tools and methods.
+ Familiarity with Configuration, Requirements, and Documentation Management tools (e.g. GitHub, Jama, DOORS, JIRA, etc)
+ Strong analytical and problem-solving skills and clear, concise documentation writing skills
+ Excellent verbal and written communications skills and the ability to communicate complex ideas succinctly and persuasively to peers, management, customers and partners.
Additional Skills/Preferences:
+ Proven record of taking customer safety requirements from concept to final product.
+ Experience in working with certification bodies to gain product certification to ISO26262
+ Experience in fault injection techniques
+ Experience in development of software safety diagnostic routines
+ Experience in Software Quality and process (e.g., SPICE, CMMI).
+ Experience of applying MISRA standards in software development
+ Knowledge of ISO 9001 Quality Management standard
+ Knowledge of cybersecurity and ISO21434
Cadence is committed to equal employment opportunity and employment equity throughout all levels of the organization. We strive to attract a qualified and diverse candidate pool and encourage diversity and inclusion in the workplace.
Travel: Occasional travel, including international travel, will be required.
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E-Verify Cadence participates in the
E-Verify program in certain U.S. locations as required by law. Download More Information on E-Verify (64K) ( plays a critical role in creating the technologies that modern life depends on. We are a global electronic design automation company, providing software, hardware, and intellectual property to design advanced semiconductor chips that enable our customers create revolutionary products and experiences.
Thanks to the outstanding caliber of the Cadence team and the empowering culture that we have cultivated for over 25 years, Cadence continues to be recognized by Fortune Magazine as one of the 100 Best Companies to Work For. Our shared passion for solving the world's toughest technical challenges, our dedication to pushing the limits of the industry, and our drive to do meaningful work differentiates the people of Cadence.
Cadence is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, basis of disability, or any other protected class.
Cadence is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, basis of disability, or any other protected class.
Affiliate Safety Representative

Posted 4 days ago
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AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are seeking an Affiliate Safety Representative to join our Citywest office in Dublin. In this role, you will lead the coordination and implementation of all pharmacovigilance activities, ensuring that AbbVie's legal and ethical obligations are fulfilled. You will serve as the primary contact for the Affiliate on pharmacovigilance matters, liaising with the National Regulatory Agency and AbbVie's Pharmacovigilance and Patient Safety (PPS) function. This position provides strategic leadership for managing and supporting the pharmacovigilance team in carrying out their duties. It reports directly to the Affiliate Medical Director, with an additional indirect reporting line to the EU Qualified Person for Pharmacovigilance (QPPV) for all PV-related issues.
Responsibilities:
+ Foster effective business relationships across the affiliate to implement patient safety standards.
+ Enhance PV systems through continuous improvement and collaboration with PPS experts.
+ Support recruitment, training, coaching, and performance management of PV staff.
+ Monitor affiliate PV compliance, workload, and resource management.
+ Address compliance issues and ensure PV processes for digital media and internet safety data.
+ Ensure local SDEAs meet AbbVie procedures and local requirements; manage inventory in PPS PV Agreements Database.
+ Maintain compliance with local agreements.
+ Serve as key contact for internal PV audits and regulatory inspections.
+ Ensure timely audit responses and corrective actions; support vendor audits and corrective plans.
+ Collaborate with Affiliate Risk Management Team to review RMPs and implement risk minimization measures.
+ Develop and revise Local RMPs with ARMT & Benefit Risk Management Team.
+ Monitor medicinal product safety profiles and emergent concerns.
+ Communicate safety data changes to PPS Product Safety Team Lead and EU QPPV.
+ Establish after-hours reporting and disaster recovery plans for critical PV processes.
+ Strengthen relationships with affiliate colleagues and enhance understanding of PV requirements.
Qualifications
+ Degree in medical, pharmacy, or life sciences (or equivalent).
+ Minimum of 2-5 years in a pharmacovigilance role within the pharmaceutical industry is required; experience managing direct reports is preferred.
+ Excellent written and verbal communication and presentation skills.
+ Fluency in written and spoken English is essential for communication with Pharmacovigilance and Patient Safety, Area/Regional Medical, and other headquarters functions. Fluency in the local language is required for interactions within the affiliate medical department and with the National Regulatory Agency.
+ High focus on customer service.
+ Strong commitment to adhering to all relevant regulations and guidelines.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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