147 Oil & Gas jobs in Ireland

**Summary:**
Production Engineers (PEs) at Meta are specialized software engineers who develop the underlying infrastructure for all of Meta's products and services, forming the backbone of every major engineering effort that keeps our platforms running smoothly and scaling efficiently.PEs work across Meta's product and infrastructure teams to ensure our services are reliable, performant, and capable of supporting billions of users. This means writing high‑quality code, solving complex problems in live production, and tackling challenges that impact over 2 billion people worldwide.Our PEs are embedded in teams across the spectrum - from products like Instagram, WhatsApp, Oculus, and Videos to critical backend services such as Storage, Cache, and Networking. The team brings together diverse levels of experience and backgrounds. Working alongside some of the best engineers in the industry, you'll contribute to code and systems that go into production and are used by millions every day. In Production Engineering at Meta, we navigate uncharted waters daily - solving problems at a scale few others face.
**Required Skills:**
Production Engineer Responsibilities:
1. Own the end-to-end reliability and scalability of the platforms, services, and products built on top of Meta's underlying infrastructure and network
2. Write and review code, develop documentation and capacity plans, and debug the hardest problems, on some of the largest and most complex systems in the world
3. Together with your engineering team, you will share an on-call rotation and be an escalation contact for live service incidents
4. Partner alongside the best engineers in the industry on the coolest stuff around, the code and systems you work on will be in production and used by billions of users all around the world
**Minimum Qualifications:**
Minimum Qualifications:
5. 4+ years experience coding in higher-level languages (e.g., PHP, Python, C++, Rust or Java)
6. 4+ years experience building, maintaining, and debugging production services/platforms such as cloud infrastructure, load balancers, relational databases, and messaging systems
7. 4+ years experience with software development, frameworks and APIs
8. Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience
**Preferred Qualifications:**
Preferred Qualifications:
9. Depth of understanding in an areas such as operating systems or TCP/IP network fundamentals
10. Experience with distributed web-scale & Data systems
**Industry:** Internet

Location: Waterford
Job Type: Regular, Full-time, 5 days on-site
**About the Opportunity**
Reporting directly to the Head of Lyo Fill Finish Operations and as a leader for Sanofi, you will play an integral role within the Fill Finish Autonomous Production Unit management team, ensuring reliable supply of lyophilised vial products to our rare disease patients globally.
**About Sanofi Business Unit**
The multiple national award-winning Sanofi Waterford biopharmaceutical and medical device campus is located in Waterford on Ireland's southeast coast. Established in 2001 and now with more than 900 employees, the site has seen more than 600m invested in state-of-the-art infrastructure and technology. Diversification continues to bring new products to Waterford and the expanded site portfolio continues to create new opportunities.
**Key responsibilities**
+ Lead all assigned operations activities to ensure that objectives are met; turnaround time, batch release cycle time, annual planning, project and program implementation etc
+ Develop and lead a continuous improvement program that will result in savings to COGs
+ Ensure all activities are undertaken in compliance with cGMP and Safety standards
+ Ensure all employees, for which they are responsible, are trained against SOPs and GMP requirements relevant to their job
+ Ensure procedures are correctly defined and followed.
+ Monitor the level of GMP compliance in their area on an on-going basis through audit, deviations and GMP document reviews
+ Develop and improve the effectiveness of training on a regular basis
**About You**
To excel in this role you will need to have:
**_Essential requirements:_**
Higher level Diploma/Degree in Third level qualification or equivalent
+ Minimum 2 years' experience as an Operations Manager/ other Management role
+ Minimum 1 years experience of pharmaceutical manufacturing environment
+ Technical knowledge of relevant manufacturing technology
+ Detailed knowledge of cGMP
+ Excellent interpersonal skills - active listener
+ Good problem solving and analytical skills
+ Effective facilitator
+ Influences site KPI's
+ Full understanding of Health &Safety and legal requirements for the safe operation of his team
**It would be advantageous to have (not essential):**
+ Sterile Operations experience
+ cGMP experience in a management position
**What Sanofi can offer you**
+ A role where you are instrumental to ensuring reliable supply of critical products to a global patient population, in an environment where you can develop and grow a meaningful career.
+ We offer a generous package including flexible benefits, and are committed to helping you have a healthy work-life balance throughout your career with us
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (

**Program Manager, NPI**
Role: Permanent
Location: Stryker Anngrove, Cork
Type: Hybrid
As a Program Manager, you will be joining the Advanced Operations, New Product Development team. In your role, you will lead your global teams on complex projects in developing the high quality new products in global footprint and ensure completed on-time and within budget. You will support cutting edge medical device products from the early inception phase to launch. You are expected to lead strategically-critical projects or programs to ensure timelines and goals are met/communicated appropriately.
**What you will do:**
+ Lead teams to maintain the governance structure for AO Foot & Ankle project portfolios, including tools, templates, reporting cadence, and compliance requirements.
+ Manage AO F&A project portfolio. Work with project managers and resource managers to ensure resources are appropriately assigned and managed.
+ Ensure all F&A projects follow standard PMO methodologies and processes (e.g., phase gates, risk management, resource planning).
+ Collaborate with BU leadership to define, manage and own program scope. Create detailed Work Breakdown Structure.
+ Develop and manage the detailed program Gantt chart. Analyze critical path, major workstreams, and intersecting milestones. Own the program schedule. Monitor and track the status
+ Create program budget with cross-functional managers and directors. Optimize, monitor, and maintain costs within budget.
+ Partner with project teams to create program Quality Plans using a multitude of quality planning tools and techniques. Monitor and maintain plans.
+ Develop a risk management plan for the program. Identify, analyze, and understand project risks, develop and monitor a risk response plan.
+ Develop a Procurement Management Plan and be a strategic partner in the selection of procurement partners.
+ Develop a Stakeholder engagement plan for the program, based on the identification, analysis and understanding of Stakeholder expectations and requirements.
+ Develop and Execute communications management plan for program team, key stakeholders, and business leaders.
+ Incorporates end-user feedback to refine scope through the project lifecycle and can communicate changes, updates, and decisions to key stakeholders
+ Builds successful working relationships with internal and external personnel in various departments. Understands quality system(s).
**Required Qualifications**
+ B.S. in a scientific or engineering field preferred; business will be considered in conjunction with experience required.
+ 8+ years of work experience required; 5+ years of project management experience preferred.
**Preferred Qualifications (Strongly desired):**
+ Proven track-record: experience successfully completing multiple projects delivering products or solutions as a project manager.
+ Adept at team management: selects the right people to the right tasks all while maintain team morale and recognizing contributions.
+ Can influence without direct authority in a way that makes others want to be on their team.
+ Can understand and communicate how goals fit into broader organizational goals and prioritize tasks/schedule accordingly.
+ Experience working in a regulated environment
+ Proficient in Microsoft Project with experience creating and regularly maintaining project timelines.
+ Keeps the customer at the heart of what we do
+ Exercises good judgment and can weigh benefits and risk to make solid decisions despite ambiguity
+ Growth mindset - ability to learn quickly and adapt to a changing environment
+ Additional role-specific knowledge and capabilities may be added as deemed necessary by the local hiring manager.
**Preferred Skills / Engineering tools:**
+ PMP or PgMP or equivalent preferred
+ Microsoft Project and/or Smartsheet's
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

**Senior Operations Manager - Stryker Tullagreen, Cork**
Due to significant growth, we are looking to hire a Senior Operations Manager to join our Stryker Tullagreen manufacturing site in Cork, in collaboration with our customers, we are mission driven to make healthcare better by providing innovative orthopaedic and spine implants which help to improve patient outcomes daily.
Here you will be a key member of the Site Leadership Team with responsibility for Site Strategy, Future Capacity Planning & the gate keeper for NPI's, PT's and MT's. This role will suit someone who puts people first, has a track record of developing top talent, has strong business acumen and an ability to understand technical manufacturing processes.
**What You will Do:**
+ Day-to-day effective management of production, ensuring products are produced in a timely and cost-effective manner.
+ Has demonstrated ability to lead teams to deliver a quality first culture, customer service, enabling growth, continuous improvement of products and processes and drive engagement of the operations teams, while ensuring alignment to Stryker Corporate and SGS requirements and standards.
+ Mentor to other Operations Managers.
+ Establish performance targets for the Business Unit(s), and monitor actual Business Unit performance against targets, taking appropriate and timely corrective action where negative trends begin to emerge.
+ Leadership of one or multiple high performing teams across units, provides guidance / direction to the operational and functional areas on site, fostering an environment of proactive and continuous improvement approach.
+ Mentors and coaches other Operations Managers
+ Ensure that sufficient processes are in place for capacity planning so the organisation's commitment to meets or exceeds customer requirements are met.
+ Sponsors an environment of Safety, Quality, People Development and CI within Stryker by working with business partners to define expected standards and the roles/responsibilities in the conservation of these standards.
+ Champions a positive employee environment by promoting open communication, engagement, and development of quality teams. Promotes a culture of inclusiveness, trust, flexibility, and teamwork.
+ Ensures effective processes in selection of competent talent and supports the development of future potential experts and leaders. Ensures effective training and performance management processes are in place and executed.
+ Sponsors and ensures engagement in all internal and external audit programmes such as Corporate, notified body & FDA audits.
+ Oversight and responsibility to ensure operation units maintains adherence to all KPI's (Safety, Quality, Service, Cost, and People Development). Continuously monitors and partakes in Local and global forums to assess opportunities for improvement.
+ With global alignment, ensures that necessary Capacity is in place across the network to meet our Customers' Demands.
+ Represent the Operations function in NPI launches, ensuring availability of resources and FG product to meet agreed launch plans.
+ Foster strong collaboration across all functions, has a strategic view in identifying alignment and developing strategies.
+ Contribute as a key member of SYK Site Management Team to develop and implement an operational execution plan for the site
+ Build a high trust and engagement culture within operations. Lead and demonstrate behaviors that drive engagement every day.
+ Build and develop talent within the function and site. Support and mentor other team members as required and participate in talent review process outside of own area
+ Ensure effective performance management, communications, and recognition within function.
+ Supporting and / or managing major CI Programs as required, which may include being involved at any or all phases of project / program from idea to execution phase.
+ Project manage the more complex improvement initiatives as required
+ Support Standardising approaches and practices across Operations Locally and Globally.
+ All other duties as required
**What You Need:**
+ At least 5 years manufacturing experience, preferably at production management level, within a team-based manufacturing environment (Medical Device background desirable but not essential).
+ Degree in Mechanical/Production Engineering or equivalent essential.
+ An excellent team player that can leverage the abilities of all personnel working within the business unit.
+ Competent in preparing business strategies and implementing action plans.
+ PC literate and strong knowledge of inventory systems, MRP and measurement tools essential.
+ Excellent presentation and communication skills are required.
+ Individual must be challenged by a team-based environment, which places high degree of emphasis on accountability for service levels, inventory management, standard cost, and expense control and quality/GMP compliance.
+ Strong leadership skills, persuasive but firm and decisive when necessary, and can demonstrate success in managing change, developing the team, and confronting performance issues (such experience in a unionized environment an advantage but not essential).
+ Competent in preparing business strategies and implementing action plans.
+ An excellent team player that can leverage the abilities of all personnel working within the business unit
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

**About Abbott**
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 113,000 colleagues serve people in more than 160 countries.
**Abbott in Ireland**
Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford, and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations, and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
**Abbott Ireland Nutrition Division Cootehill Cavan**
Abbott Nutrition produces a range of infant formulae in all pack sizes under the brand name "Similac". To complement the range of "Similac" infant formulae, the facility also manufactures a range of follow-on formulae under the brand name of "Gain". The essential ingredient is liquid skim-milk and this is combined with carbohydrate, vegetable oils, vitamins and minerals. The product is blended, pasteurised, dried and packaged at the site and once packaged, is distributed to Europe, Southeast Asia, the Middle East, Latin America and Canada.
Established in 1975, Abbott Nutrition in Ireland is the largest powder manufacturing facility for the production of infant formulae within the Abbott Corporation worldwide. Approximately 1,000 dairy farms in Ireland and Northern Ireland supply quality milk to the Cootehill facility which processes 500,000 litres per day. This secure supply together with Ireland's reputation as a green, clean environment is of significant strategic importance to Abbott Nutrition.
**Primary Function I Goals / Objectives**
- The Food Safety Specialist has the responsibility for reviewing all SOP's for any job task he/she may carry out and ensure he/she fully understands and adheres to the SOP.
- The Food Safety Specialist provides guidance and direction of plant sanitation for manufacturing operations, warehouse and plant grounds.
- The purpose of the job is to implement food safety, sanitation, and regulatory compliance policies, procedures and training.
- This Job function will change where update procedures to GMP, EHS, Technical/ New Equipment, Quality Procedures & SOP's are made.
- This list of responsibilities may change depending on plant needs and employees are expected to be adaptable and flexible were this need arises.
**Major Responsibilities**
The role of the Food Safety Specialist is part of the site's success and compliance by:
- Driving and implementing holistic plant sanitation programs, policies and procedures for plant, warehouse and plant grounds; Assuring compliance with all local, state and federal regulations and all food safety policies and procedures
- Acting as sanitation support in the process of assessing and mitigating safety risk associated with construction and major maintenance.
- Collaborate/Coordinate with Facility Supervisor, Operations Leadership, Operations Associates and Site Cleaning staff to achieve desired Environmental Monitoring performance and Pest Control performance
- Evaluating facility sanitary conditions, assessing risk based on food safety and public health principles, prioritizing corrective actions, and verifying sanitation activities and validation testing
- Evaluating monthly environmental samples for monitoring of pathogenic organisms in plant, trending the results and developing corrective actions
- Conformance to master cleaning schedule and applicable cGMP guidelines, best practices and requirements.
- Assist in developing and implementing all sanitation related training for sanitation and plant employees as needed;
- Ensures all safety requirements related to sanitation are met including proper
chemical storage, MSDS, PPE (Personal Protective Equipment) and procedures.
- Maintaining and writing detailed clean up procedures and Sanitation Standard Operating Procedures for all plant equipment, driving towards reduced water and air usage.
**Education & Experience**
You will have BSc a in plant quality/food safety/Sanitation with a minimum of 3yrs experience in a similar role with demonstrated Leadership skills (direct or cross functionally leadership skills)
Certification as a Sanitarian and Pesticide Application is an advantage for this role
**Key Skills:**
- Understanding and application of microbiological principles with in depth food borne pathogen knowledge.
- Knowledge of HACCP, Sanitation principles and Food Safety Preventive Controls (FSPC)
- Understanding of the appropriate wet cleaning and dry cleaning methodology.
- Experience in successfully addressing environmental sanitation challenges in areas such as drains, floors, walls, roofs, and equipment.
- Proven leadership capabilities
- Project planning & execution experiences
- Process control knowledge
- Proven plant financial understanding
- Experience with working on Continuous Improvement Projects
- Experience with Word, Excel, PowerPoint, etc.
**Accountability / Scope**
- The Food Safety Specialist works under the direct supervision of the Food Safety Manager. Position assists and with all phases of sanitation, pest control, microbiological and cleaning programs for the site. The decision-making process of this position is key to the ongoing compliance of the production operation, and to the quality and safety of the food products.
Connect with us at on LinkedIn at , on Facebook at and on Twitter @AbbottNews.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

Req ID: 128082
Remote Position: No
Region: Europe
Country: Ireland
State/Province: Galway
City: Galway
**General Overview**
**Functional Area:** Quality (QUA)
**Career Stream:** Operations Quality (OPQ)
**Role:** Senior Manager (SMG)
**Job Title:** Senior Manager, Operations Quality
**Job Code:** SMG-QUA-OPQ
**Job Level:** Level 11
**Direct/Indirect Indicator:** Indirect
**Summary**
The Senior Manager, Global Quality for HealthTech is responsible for the global HealthTech quality team in Celestica Galway to establish and maintain a quality-first culture across worldwide manufacturing facilities. This involves managing a large global organization, collaborating with customers, suppliers, and partners, and ensuring compliance with regulatory requirements (FDA, ISO, ASQ, RAC).Significant experience with FDA certification processes is required.
**Detailed Description**
Candidate Profile
The Senior Manager, Global Quality for HealthTech in Celestica Galway will be a strategic visionary with a strong operational background, a customer-centric approach, and a proven ability to deliver results. This individual will be an accomplished and strong leader with excellent communication and interpersonal skills, able to quickly establish and maintain strong cross-functional relationships with key stakeholders. The successful candidate will have a proven history of driving operational excellence and achieving business goals in a complex and dynamic environment.
Responsibilities:
Develop and implement the global quality strategy in collaboration with regional and site leadership, identifying gaps and creating short and long-term plans.
Share best practices across HealthTech teams and host quality forums for issue discussion, decision-making, and plan execution.
Establish the HealthTech Quality Strategy (e.g., MDSAP / EU MDR).
Define annual quality objectives and metrics aligned with business priorities, driving quality culture and performance improvements.
Oversee the quality management system globally, including industry certifications, customer surveys, operational reviews, and system applications.
Cultivate an "audit-ready" culture and direct the Global Regulatory Compliance Audit Program, ensuring internal audits are effective and findings are tracked to closure.
Conduct Quality Management Reviews and training with manufacturing sites and executive management, advising on risks and mitigation plans.
Maintain an effective 8D reporting system for quality issues and resolutions, involving cross-functional staff.
Manage talent within the Quality team, including hiring and training.
Provide program management leadership for special projects and initiatives and guide quality communities and internal teams.
**Knowledge/Skills/Competencies**
Strong relationship management and interpersonal skills.
Proficiency in Microsoft Office for data analysis and reporting.
Understanding of validation principles and testing procedures.
Knowledge of FDA, ISO, RAC, and CQA regulations and standards.
Willingness to travel internationally (15%+).
Education:
Degree in Engineering or Sciences required.
RAC(US), CQA, ASQ, or ISO/RABSQA Auditor Certification is desirable.
Experience:
10-12 years in quality management and related functions (Manufacturing Quality, Design Quality, Validation, Quality Assurance, Quality Systems).
Minimum 5 years conducting quality audits.
Experience with FDA and regulatory inspections.
In-depth knowledge of quality management systems and global compliance.
Experience in the HealthTech industry.
Global and multi-site leadership experience.
Experience in driving cultural change for quality awareness.
**Physical Demands**
+ The job works in generally good conditions with occasional exposure (10% - 33%) to noise, odours, dust, drafts, chemicals, operating machinery, temperature extremes, hazardous substances, etc.
+ Duties may require extended periods of sitting and sustained visual concentration on a computer monitor or on numbers and other detailed data. Sustained visual concentration on numbers, legal documents.
+ Occasional overnight travel is required.
**Notes**
This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time.
Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law).
At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them.
**COMPANY OVERVIEW:**
Celestica (NYSE, TSX: CLS) enables the world's best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development - from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud. Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers.
Celestica would like to thank all applicants, however, only qualified applicants will be contacted.
Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services.

**About Abbott**
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Abbott in Ireland**
Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo.
**Abbott Diabetes Care Kilkenny**
Abbott Diabetes Care has opened a new site, in Kilkenny, that is at the forefront of Diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems.
**This is how you can make a difference:**
As a Quality Operations Manager you will guide our team of Quality Team Leads and Engineers. In this role, you will be pivotal in ensuring our site delivers safe and effective products that meet customer needs while maintaining compliance. You will implement quality standards and execute compliance at every stage of the process.
**Key Responsibilities:**
+ Lead a team of quality professionals to achieve individual, team, and site goal.
+ Develop and implement quality assurance strategies and regulations.
+ Ensure compliance with Quality, Abbott Division, and Corporate Procedures and Standards by developing and implementing all required Quality and EHS documentation.
+ Assess potential risks, ensure compliance, and provide recommendations.
+ Take responsibility for all quality control aspects of the process, including laboratory studies, clinical research, testing, operations, raw materials, production, and finished products or services.
+ Facilitate audits and regulatory inspections.
+ Liaise with external vendors, contractors, or suppliers to ensure their products or services meet our organization's quality standards.
+ Coordinate quality training sessions.
+ Implement quality standards and ensure compliance at every stage of the process.
**Education and Experience:**
+ Minimum NFQ Level 8 in Science/Engineering or a relevant qualification.
+ At least 2 years of experience in a similar position.
+ Proven problem-solving abilities.
+ Quality management experience gained in a regulated industry is essential.
**Why Join Us?**
We offer competitive salaries, comprehensive benefits, and opportunities for professional development.
If you're passionate about quality management and want to make a difference in a dynamic team, we encourage you to apply today!
Connect with us at and on LinkedIn , Facebook ( , Instagram , X ( and YouTube .
Abbott is an equal opportunities employer.
#LI-SO2
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

**Summary:**
You will be joining the team that is responsible for the design and implementation of Meta's global core IP networks (Express Backbone). The team is responsible for the routing platforms, protocols, and architecture that connect Meta's data centers to each other as well as to the networks that connect them to the internet.Our backbones continue to rapidly expand globally, based on the, most recently, network demands that our AGI journey brings. One of them, "Express Backbone", handles machine to machine traffic between our Data Centers.You are an experienced network engineers with demonstrated experience in software engineering, who regularly perform analytical and data-driven dives into the workings of the backbone but also hold manufacturers to deliver and scale their products and work in cross functional environment. You will have a chance to participate in designing and growing of one of the largest backbone networks in the world.
**Required Skills:**
Network Production Engineer - Core Networking, Backbone Responsibilities:
1. Propose, describe and develop designs to scale Express Backbone to meet the business demand.
2. Participate and drive migration processes from one design to the next iteration through cross-functional engagement.
3. Perform analytical and data-driven dives on complex technical issues across networks, ranging from automated tooling to hardware failures and network issues.
4. Manage and maintain multi-vendor relationship and provide quality feedback to drive vendor's development.
5. Contribute to team growth and development through new hire onboarding and peer mentorship.
6. Help with the process of finding a root cause for the Express Backbone issues.
7. Be an escalation contact for high-impact, high-priority incidents.
**Minimum Qualifications:**
Minimum Qualifications:
8. Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience.
9. 2+ years of experience coding in higher-level languages (e.g., Python, C++, Go, etc.).
10. 5+ years of experience in one or more of BGP, MPLS, ISIS or similar routing protocols - knowledge in typical configurations and performance tuning.
**Preferred Qualifications:**
Preferred Qualifications:
11. 5+ years of experience understanding and mitigating network hardware and topology failures.
12. Proficient level knowledge of TCP/IP and IPv6.
13. Experience operating and designing Software Defined Networking-based backbone networks.
14. Knowledge in routing and switching - hardware design and knowledge of forwarding and data planes.
15. Experience developing and understanding network device configuration for at least one vendor (Juniper, Cisco, Arista, Brocade, etc.).
16. Experience working in a multi-vendor network environment.
17. Experience with developing distributed systems and operating them at scale.
18. Experience with automation frameworks and tools such as Ansible, Puppet, or Chef.
19. Experience in configuration and maintenance of network devices and Network Management Systems, or applications such as web servers, load balancers, relational databases, storage systems and messaging systems.
20. Experience learning software, frameworks, and APIs.
**Industry:** Internet

**Summary:**
Meta is seeking a forward-thinking experienced Engineer to join the Production Operations Engineering team within Infra Data Centers. Our data centers, and the hundreds of thousands of servers installed in them, are the foundation upon which our rapidly scaling infrastructure efficiently operates and upon which our innovative services are delivered. Meta is at the leading edge of the global data center industry both in terms of how data centers are designed and operated. This person should enjoy working in a fast paced, technical environment where adaptability and flexibility will be key to their success. We seek an IT professional with advanced, hands-on technical skills in server hardware and Linux (ideally in a Data Center environment). Having extensive knowledge of server administration and performing on complex projects in a large-scale distributed data center environment is a core competency of this individual. The candidate should also have practical knowledge and experience in at least one of the following core areas: Hardware, OS repair, Tooling and Automation and Project Management.
**Required Skills:**
Data Center Production Operations Engineer Responsibilities:
1. Perform dives and analyze complex technical issues within the data center, ranging from automated tooling to hardware failures, Linux OS, and network issues
2. Work as a subject matter expert with cross functional teams on large scale data center projects and initiatives
3. Provide cross data center support and identify potentially larger issues, displaying effective communication when something is identified
4. Work with internal hardware teams and vendors to help drive complex technical issues to resolution, provide an ownership stake in ensuring high quality levels of hardware, and influence future design to ensure ease of serviceability
5. Capacity to solve issues at scale using scripting, automation and tooling
6. Use data to drive maximum server fleet up-time and utilization rates, by understanding hardware failure rates and Service Level Agreements to customers. Identify trends and systemic issues in the fleet and drive resolution
7. Coach/Mentor team members to evaluate and identify better ways to resolve issues and define updates to tools and processes
8. Provide mentorship and be the go-to technical resource for management
9. Build cross functional relationships and have the experience to influence policies and procedures to improve global data center operations
10. Participate in an on-call rotation
11. Daily use of our ticketing system to support servers that are unavailable and need to be returned to capacity
**Minimum Qualifications:**
Minimum Qualifications:
12. BS, BA or BEng in technical field or commensurate experience
13. 5+ years of infrastructure or related experience
14. Knowledge of Linux and hardware systems support in an Internet operations environment
15. Experience managing multiple technical issues concurrently
16. Knowledge of the interdependencies of data center functions and technologies including electrical, cooling, structured cabling, security, network and server systems
17. Knowledge of out-of-band/lights-out server communication methods, such as IPMI and serial console
18. Time and project management experience
19. Experience in modifying and developing in commonly used scripting or programming languages
**Preferred Qualifications:**
Preferred Qualifications:
20. Experience with large-scale GPU based systems
21. Experience in debugging, modifying and developing in commonly used scripting or programming languages including Bash, PHP, Python, SQL, or Perl
22. Experience in a large-scale data center environment
23. Experience in providing technical guidance to external vendors
**Industry:** Internet