3 Jobs in Enniscorthy

**Job Description Summary**
As the Process Development Engineer, you will actively participate as a key cross-functional team member on new product development projects with a focus on design for manufacturability and the design, development, implementation and validation of manufacturing processes, test methods and equipment.
**Job Description**
**We are the makers of possible**
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
**Why join us?**
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
Become a **maker of possible** with us!
**Main responsibilities will include:**
+ Lead the design, development, implementation, and validation of manufacturing processes for new products. This will include leading process development reviews, communicating process status and plans.
+ Participate in regular project meetings and reviews with cross-functional team members to track project status and effectively follow up on action items
+ Communicate with cross-functional team members and suppliers to understand and determine product process and equipment specifications
+ May supervise or manage technicians, engineering interns or associate engineers
+ Document process development including manufacturing procedures, protocols, and reports
+ Develop and maintain a broad knowledge of product design, manufacture, and assembly techniques
+ Estimate resource requirements, workload assignment, production times for manufacturing processes
+ Train technicians, operations and quality assurance on new design and process development and test methods
+ Manage the manufacturing site selection process based on the evaluation of internal manufacturing sites, suppliers, and contract manufacturers
+ Participation in or creation and control of a project budget (expense and/or capital expenditure)
+ Participate as a subject matter expert and/or lead design and technology transfers to manufacturing
**About you:**
+ B.S. degree in an engineering discipline is essential.
+ 4+ years of industrial experience in process development, preferably in medical device or other regulated FDA/QSR and ISO environment.
+ Demonstrated hands-on technical aptitude with knowledge of cGMP and GLP.
+ Working knowledge of DOE and other statistical methods.
+ Strong written, communication, and interpersonal skills with the ability to lead cross functional teams.
+ Ability to analyse data, interpret results, and write reports. With the ability to create and execute project plan.
+ Basic tooling, design and drafting knowledge.
+ Training in Six Sigma or Design for Six Sigma.
+ Experience in design and technology transfers.
+ Experience with process validation (IQ, OQ, PQ) is distinct advantage.
+ PMO certification is a distinct advantage.
Click on apply if this sounds like you!
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.
To learn more about BD visit: Skills
Optional Skills
.
**Primary Work Location**
IRL Wexford - Enniscorthy
**Additional Locations**
**Work Shift**
At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You ( .
Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed.
The salary or hourly rate offered to a successful candidate is determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location.
**Salary Range Information**
54,800.00 - 93,200.00 EUR Annual
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

**Job Description Summary**
The Design Quality Engineer assures that new product designs and the processes for manufacturing them meet all local, corporate and divisional requirements with respect to safety and efficacy.
**Job Description**
**We are the makers of possible**
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
**Why join us?**
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
**Become a maker of possible with us!**
**Our vision for Quality at BD**
In our Quality team, we collaborate on a large scale, focusing on making sure everything is correct, effective and efficient to bring the highest-quality and most competitive products and services to our customers and their patients.
**About the role**
This role centers on ensuring quality and risk management throughout the lifecycle of new product development (NPD) projects. The individual represents quality interests within project teams, leading quality engineering tasks and risk management activities such as UFMEA, DFMEA, PFMEA, and related documentation. They are responsible for reviewing design compliance, conducting statistical analyses (e.g., DOE), and initiating corrective actions when necessary. The role also involves supporting biocompatibility testing aligned with ISO10993, participating in internal and supplier audits, and validating test methods and measurement systems like Gauge R&R.
Candidates for this position should possess a third-level qualification in engineering, science, or a technical field, along with a minimum of five years of experience in the medical device or pharmaceutical industries. A solid understanding of regulatory standards, including ISO 13485, ISO 14971, and related CFRs, is essential. Preferred skills include attention to detail, adaptability, strong problem-solving abilities, and excellent interpersonal skills.
The role requires someone who can manage multiple projects independently while collaborating effectively in team settings and meeting deadlines consistently.
**Main responsibilities will include:**
+ Represents quality interests and concerns on project teams.
+ Leads risk management activities and owns the Quality engineering activities for NPD projects.
+ Must be able to balance multiple projects and tasks, from product inception through product launch and maintenance.
+ Review design control compliance requirements for NPD projects and all design elements.
+ Is responsible for the development of the UFMEA & DFMEA, coordinating guidance from the other design sub-team members and supporting the development of the PFMEA.
+ Performs DOE's and other statistical analysis to support product and process optimisation or resolve causes of process variation. Initiate corrective actions as required.
+ Supports assessment of Biocompatibility testing required as per ISO10993 and company procedures.
+ Participates in internal audit and supplier audit programmes.
+ Risk management - U/DFMEA; Risk Analysis, Risk Management File and Gauge R&R and Test Method Validation.
**About you**
+ Third-level Engineer / Technical / Science Qualification
+ Minimum of 5 years in the medical device or pharmaceutical industry is desirable
+ Familiarity with regulations including ISO 13485, CFR 11820, ISO 14971 and CMDR.
+ Attention to detail and adaptability
+ Dedication to excellence, flexibility
+ Problem-solving techniques with excellent organization skills
+ Excellent interpersonal skills with the ability to work in a team environment and work under own initiative to target and deadlines
**Click on apply if this sounds like you!**
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
**To learn more about BD visit:** ** Skills
Optional Skills
.
**Primary Work Location**
IRL Wexford - Enniscorthy
**Additional Locations**
**Work Shift**
At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You ( .
Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed.
The salary or hourly rate offered to a successful candidate is determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location.
**Salary Range Information**
43,300.00 - 73,600.00 EUR Annual
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.