73 Weekend Staff jobs in Ireland

**Operations Supervisor - Stryker Model Farm Road**
Shift = Weekend: 7:00am to 7:00pm Fri, Sat, Sun (shift allowance applies)
Due to continued growth, we are seeking an Operations Supervisor to join our Neurovascular facility on Model Farm Road, Cork. In this role, you'll have the opportunity to lead, inspire, and mentor diverse teams across our site. We believe in winning together-by doing things the right way, challenging one another, and always striving for excellence. Our passion, purpose, and integrity set us apart. At Stryker, you'll experience unmatched energy, opportunity, and a shared commitment to making a difference-for our customers, for patients, and for our Stryker family
**What you will do:**
+ Leads a production team to ensure targets/KPIs for quality/service/costs/people development are achieved.
+ Ensures quality standards and expectations are communicated and deployed. Quality standards and objectives (rework, scrap, line clearance, QA audits, cell/value stream shutdown) are communicated and achieved.
+ Manages and prioritises production to meet customer requirements and maintain inventory levels. Communicate and manage output levels.
+ Sets team and individuals up for success by providing training, coaching, feedback and support.
+ Creates a positive employee relations environment and facilitates high engagement within the production team and with the cross functional team.
+ Provides timely feedback and review, and ensures all performance issues are dealt with in a constructive, fair and prompt manner. Ensures that all employees are treated with fairness and respect.
+ Facilitates open two-way communications regarding individual, team and company performance through weekly team meetings and daily interaction on the line with a view to optimising efficiency and productivity.
+ Liaises with training to develop and implement training curriculums and team training plans.
+ Participates in the selection and hiring of Production Operators
+ Maintains GMP / 6S at a high level within the department through the involvement of all team members.
+ Lead / participate in continuous improvement activities, e.g. Lean/Cost Reduction initiatives
+ Ensures Time and Attendance system compliance and effective Annual Leave and Overtime planning
+ Provides leadership and direction for the advancement of Lean Manufacturing
+ All other duties as assigned.
**What you will need:**
+ Degree or Masters in Business, Production Management, Engineering or similar Discipline or demonstrated equivalent experience
+ 4 years minimum experience in a manufacturing environment.
+ 2 years minimum Supervisor experience.
+ Good knowledge of GMP / FDA regulatory requirements, housekeeping, health and safety.
+ Genuine interest in investing in people and facilitates individual and team engagement and development.
+ Ability to coach, provide effective feedback and manage performance.
+ ·Problem solving methodology experience required with process knowledge desirable.
#IJ
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.

Operations Supervisor - Stryker Model Farm Road Shift = Weekend: 7:00am to 7:00pm Fri, Sat, Sun (shift allowance applies) Due to continued growth, we are seeking an Operations Supervisor to join our Neurovascular facility on Model Farm Road, Cork. In this role, you'll have the opportunity to lead, inspire, and mentor diverse teams across our site. We believe in winning together-by doing things the right way, challenging one another, and always striving for excellence. Our passion, purpose, and integrity set us apart. At Stryker, you'll experience unmatched energy, opportunity, and a shared commitment to making a difference-for our customers, for patients, and for our Stryker family What you will do: Leads a production team to ensure targets/KPIs for quality/service/costs/people development are achieved. Ensures quality standards and expectations are communicated and deployed. Quality standards and objectives (rework, scrap, line clearance, QA audits, cell/value stream shutdown) are communicated and achieved. Manages and prioritises production to meet customer requirements and maintain inventory levels. Communicate and manage output levels. Sets team and individuals up for success by providing training, coaching, feedback and support. Creates a positive employee relations environment and facilitates high engagement within the production team and with the cross functional team. Provides timely feedback and review, and ensures all performance issues are dealt with in a constructive, fair and prompt manner. Ensures that all employees are treated with fairness and respect. Facilitates open two-way communications regarding individual, team and company performance through weekly team meetings and daily interaction on the line with a view to optimising efficiency and productivity. Liaises with training to develop and implement training curriculums and team training plans. Participates in the selection and hiring of Production Operators Maintains GMP / 6S at a high level within the department through the involvement of all team members. Lead / participate in continuous improvement activities, e.g. Lean/Cost Reduction initiatives Ensures Time and Attendance system compliance and effective Annual Leave and Overtime planning Provides leadership and direction for the advancement of Lean Manufacturing All other duties as assigned. What you will need: Degree or Masters in Business, Production Management, Engineering or similar Discipline or demonstrated equivalent experience 4 years minimum experience in a manufacturing environment. 2 years minimum Supervisor experience. Good knowledge of GMP / FDA regulatory requirements, housekeeping, health and safety. Genuine interest in investing in people and facilitates individual and team engagement and development. Ability to coach, provide effective feedback and manage performance. Problem solving methodology experience required with process knowledge desirable. #IJ This role will be posted for a minimum of 3 days. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.

Shift - This role is for the Weekend shift. Working hours are 7am - 7pm, Friday, Saturday and Sunday. Who we want Performance: Deliver high quality products. Team Player: Build positive relationships with others to achieve common goals. Reliable: Manage time to effectively get the job done. A Manufacturing Operator effectively builds the products manufactured by Stryker to the required quality standard What you will do Responsible for manufacturing product in accordance with the relevant Stryker manufacturing procedures and relevant quality standards Participation in continuous improvement programmes or team projects to enhance our quality customer service and cost Monitor and verify quality in accordance with workmanship standards and operating procedures Adhere to procedures in relation to production methods, completion of documentation, current Good Manufacturing Practices and safety requirements Provide cross training to other employees Contribute as part of a team in achieving the line core metrics Build Quality into all aspects of their work by maintaining compliance to all quality requirements What you need Leaving Certificate, Trade or equivalent education level is required Previous experience in production/ assembly roles is desirable Basic mathematics and good English skills Good communication skills Willingness to work in a team and promote teamwork Previous experience in production/ assembly roles is an advantage The employee may be required to use protective clothing and safety equipment such as safety glasses and respirators, and the use of personal protective equipment (PPE) * Please note this is initially a 12 month fixed term contract based in our Model Farm Road location #IJ This role will be posted for a minimum of 3 days. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.

Shift - This role is for the Weekend shift.

Working hours are 7am - 7pm, Friday, Saturday and Sunday.

Who we want Performance: Deliver high quality products.

Team Player: Build positive relationships with others to achieve common goals.

Reliable: Manage time to effectively get the job done.

A Manufacturing Operator effectively builds the products manufactured by Stryker to the required quality standard What you will do Responsible for manufacturing product in accordance with the relevant Stryker manufacturing procedures and relevant quality standards Participation in continuous improvement programmes or team projects to enhance our quality customer service and cost Monitor and verify quality in accordance with workmanship standards and operating procedures Adhere to procedures in relation to production methods, completion of documentation, current Good Manufacturing Practices and safety requirements Provide cross training to other employees Contribute as part of a team in achieving the line core metrics Build Quality into all aspects of their work by maintaining compliance to all quality requirements What you need Leaving Certificate, Trade or equivalent education level is required Previous experience in production/ assembly roles is desirable Basic mathematics and good English skills Good communication skills Willingness to work in a team and promote teamwork Previous experience in production/ assembly roles is an advantage The employee may be required to use protective clothing and safety equipment such as safety glasses and respirators, and the use of personal protective equipment (PPE) * Please note this is initially a 12 month fixed term contract based in our Model Farm Road location #IJ This role will be posted for a minimum of 3 days.

To be considered for this role you will be redirected to and must complete the application process on our careers page.

To start the process, click the Apply button below to Login/Register.

Operations Supervisor - Stryker Model Farm Road Shift = Weekend: 7:00am to 7:00pm Fri, Sat, Sun (shift allowance applies) Due to continued growth, we are seeking an Operations Supervisor to join our Neurovascular facility on Model Farm Road, Cork.

In this role, you'll have the opportunity to lead, inspire, and mentor diverse teams across our site.

We believe in winning together-by doing things the right way, challenging one another, and always striving for excellence.

Our passion, purpose, and integrity set us apart.

At Stryker, you'll experience unmatched energy, opportunity, and a shared commitment to making a difference-for our customers, for patients, and for our Stryker family What you will do: Leads a production team to ensure targets/KPIs for quality/service/costs/people development are achieved.

Ensures quality standards and expectations are communicated and deployed.

Quality standards and objectives (rework, scrap, line clearance, QA audits, cell/value stream shutdown) are communicated and achieved.

Manages and prioritises production to meet customer requirements and maintain inventory levels.

Communicate and manage output levels.

Sets team and individuals up for success by providing training, coaching, feedback and support.

Creates a positive employee relations environment and facilitates high engagement within the production team and with the cross functional team.

Provides timely feedback and review, and ensures all performance issues are dealt with in a constructive, fair and prompt manner.

Ensures that all employees are treated with fairness and respect.

Facilitates open two-way communications regarding individual, team and company performance through weekly team meetings and daily interaction on the line with a view to optimising efficiency and productivity.

Liaises with training to develop and implement training curriculums and team training plans.

Participates in the selection and hiring of Production Operators Maintains GMP / 6 S at a high level within the department through the involvement of all team members.

Lead / participate in continuous improvement activities, e.g.

Lean/Cost Reduction initiatives Ensures Time and Attendance system compliance and effective Annual Leave and Overtime planning Provides leadership and direction for the advancement of Lean Manufacturing All other duties as assigned.

What you will need: Degree or Masters in Business, Production Management, Engineering or similar Discipline or demonstrated equivalent experience 4 years minimum experience in a manufacturing environment.

2 years minimum Supervisor experience.

Good knowledge of GMP / FDA regulatory requirements, housekeeping, health and safety.

Genuine interest in investing in people and facilitates individual and team engagement and development.

Ability to coach, provide effective feedback and manage performance.

Problem solving methodology experience required with process knowledge desirable.

#IJ This role will be posted for a minimum of 3 days.

To be considered for this role you will be redirected to and must complete the application process on our careers page.

To start the process, click the Apply button below to Login/Register.

Our Lady of Lourdes in Drogheda require Registrars in Paediatrics to cover Night Shifts Active IMC registration required Irish Hospital experience and references required Must have Irish/UK/EU passport OR Stamp 1G OR 4 visa Skills: Registrar Paediatric Drogheda IMC HSE Hospital Louth

Our Lady of Lourdes in Drogheda require Registrars in Paediatrics to cover Night Shifts Active IMC registration required Irish Hospital experience and references required Must have Irish/UK/EU passport OR Stamp 1 G OR 4 visa Skills: Registrar Paediatric Drogheda IMC HSE Hospital Louth

**What We Offer**
Attractive compensation package that includes **competitive pay and structure Bonus** , as well as benefits such as
+ 18.56 per Hour (inclusive of shift allowance)
+ Private Health Insurance for you and your family
+ Occupational Pension Scheme with an excellence contribution rate of 12%
+ 10% Bonus Target
+ Life assurance
+ Career Development, further education
+ Subsided onsite canteen
+ Onsite gym and access to personal trainer
+ Growing business plus access to many more benefits
+ Weekend Shift Friday to Sunday
**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 110,000 colleagues serve people in more than 160 countries.
Abbott serves the Irish market with a diverse range of healthcare products including diagnostics, medical devices and nutritionals products. In Ireland, Abbott employs over 6,000 people across nine sites. We have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford, Kilkenny 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 Vascular Division Clonmel**
Abbott Vascular is one of the world's leading vascular care businesses. Abbott Vascular is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education.
Our broad line of vascular devices-which includes vessel closure, endovascular and coronary technologies-are used to treat vessel diseases of the heart, carotid arteries and peripheral blood vessels. These vessel diseases can lead to heart attack, stroke, critical limb ischemia and other serious vascular conditions.
**Purpose of the job**
Performs a wide variety of electronic, mechanical, or electro-mechanical assembly operations on assemblies or sub-assemblies. Sets up and operates automatic or semi-automatic machines. May perform other tasks including, but not limited to; placing labels on packages, and putting data sheets with product.
**Major Responsibilities**
Responsible for compliance with applicable corporate and divisional policies and procedures.
+ Assembles, repairs, inspects and/or tests products following written instructions. Ability to read and comprehend basic instructions and other work related documents, written in English.
+ Sets up and operates a variety of manufacturing machines or equipment following written instructions in the English language.
+ Cleans tools and equipment per documented procedures.
+ Records information on approved documents.
+ Disposes hazardous waste material on corresponding hazardous waste areas.
+ Resolves problems and make routine recommendations.
+ Trains other employees when necessary.
+ Maintains all position certifications up to date as required to remain in compliance.
+ Completes daily work to meet established schedule with guidance from supervisor on prioritization of tasks.
+ Maintains confidentiality in handling sensitive information or documents.
**Education & Competencies**
+ Leaving Certificate or a pass rating in an Aptitude Test selected by Abbott Vascular
+ Relevant work experience advantageous but not essential or an equivalent combination of education and work experience.
+ Excellent communication / interpersonal skills.
+ Enthusiastic and energetic with the ability to integrate quickly into a team environment.
+ Demonstrated flexible and innovative approach to work.
+ Cognitive Skills Performs routine tasks working from detailed writtenor verbalinstructions.Assignments require limited judgement introubleshootingproven processes.
Connect with us at or on LinkedIn at on Facebook at and on Twitter @AbbottNews.
Abbott is an equal opportunities employer.
**REFER TO THE SITE SAFETY STAT** **E** **MENT (SHE ) FOR YOUR SA** **F** **ETY, HEALTH AND WELFARE AT WORK RESPONSIBILITIES**
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

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
**A Day in the Life**
**Medtronic**
At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.
**Our Purpose**
At our Manufacturing Engineering Department in Medtronic, plc, we focus on supporting product value streams to ensure that customer & patient needs are met every day. Our focus is on delivering and maintaining high maturity manufacturing processes and maintaining high-quality performance within our teams. The Engineering Supervisor is directly involved in achievement of our mission to contribute to human welfare by manufacturing products that alleviate pain, restore health, and extend life.
**_Come for a job, stay for a career!_**
**A Day in The Life Of:**
Responsibilities may include the following and other duties may be assigned:
+ Responsible for leading the Manufacturing Engineering team to meet production goals for people/safety, quality, service and cost.
+ Effectively communicates with support team leading daily meetings to manage the business and share information.
+ Develop schedules and support requirements for assigned areas.
+ Encourages and facilitates beneficial resolution of issues across the department, effectively mediates conflict to promote a friendly climate, good morale, and team cohesiveness.
+ Partners with functions to drive a continuous improvement environment.
+ Identifies opportunities to improve how we support our customers and foster a culture of innovation, identifying innovative solutions to process problems and actively encourages team members to share new ideas and fresh approaches.
+ Responsible for team's professional development to promote engagement, growth, job satisfaction and organisational health.
**Key Skills & Experience**
+ Minimum Level 8 bachelor's degree required in Mechanical, Mechatronics, Manufacturing, Electronics, Biomedical Engineering or related Engineering discipline preferred with minimum 1 years relevant experience.
+ Experience working in the medical device field will be an advantage.
+ Equipment and process fault finding and problem-solving experience required.
+ Demonstrated leadership capability with strong communication skills.
+ You will be IT proficient (MS Word/Excel).
+ Good understanding of MPS cell operations and systems.
+ Good interpersonal skills are essential, and you must be a team player.
**Medtronic offer a competitive salary and flexible Benefits Package**
**#IJA**
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
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