Medical Device Product Development jobs
- J&JLimerick, County LimerickAd
- Understanding of GMP, compliance, validation practices, system development life cycle principles and regulatory expectations relevant to a medical-device…
- J&JCork, County CorkAd
- Minimum 3-5 years’ experience working in a manufacturing environment, ideally medical device.
- Support the development & implementation of Johnson & Johnson…
View similar jobs with this employerGi Group IrelandAthlone, County WestmeathAd- Previous experience within a regulated industry, preferably medical device manufacturing, is highly desirable.
- Knowledge or experience of EU MDR requirements.
- Analog DevicesLimerick, County Limerick
- The internship program features various lunch-and-learn topics and social events with other interns and full-time employees.
- Analog DevicesLimerick, County Limerick
- Contribute to ongoing tool development and enhancement, including robotic automation improvements.
- Analog Devices International is a world-leading semiconductor…
View similar jobs with this employerBDLimerick, County LimerickAd- Strong understanding of quality management systems and regulated product development.
- Provide technical mentorship throughout new product development and…
- CplLimerick, County LimerickAd
- Significant operations management experience in the medical device or regulated life sciences sector.
- Identify opportunities for organisational development and…
- Integer Holdings CorporationGalway, County GalwayAd
- Ensure compliance at all stages of product development process (PDP).
- You will review procedures, protocols, reports, and other documents related to test method…
- Integer Holdings CorporationGalway, County GalwayAd
- Ensure compliance at all stages of product development process (PDP).
- You will review procedures, protocols, reports, and other documents related to test method…
- Collins McNicholas RecruitmentCounty Mayo
- Flexitime
- Company pension
- Private medical insurance
- On-site parking
Ad- Lead cross-functional teams through product development and commercialisation.
- Strong knowledge of product development, commercialisation and project management…
- Collins McNicholas RecruitmentAthlone, County Westmeath
- Company pension
- Private medical insurance
- On-site parking
Ad- Experience in a regulated manufacturing environment; medical device experience is highly desirable.
- We are seeking a hands-on R&D Process Technician to join…
- Collins McNicholas RecruitmentAthenry, County Galway
- Company pension
- Private medical insurance
- On-site parking
Ad- Coordinate regulatory and quality requirements alongside product development timelines.
- This is a broad, cross-functional role with responsibility for…
- BMS PerformanceCork, County CorkAd
- Experience investigating product or process quality issues.
- Excellent opportunity for a Quality Engineer looking to step into a broad, business-facing role.
- BMS PerformanceWicklow, County Wicklow
- Annual leave
Ad- Ongoing training and professional development.
- Work closely with design, production and operational teams to ensure the highest standards of product quality and…
Production Operator - 24 Month FTC
Often replies in 3 daysSanmina IrelandFermoy, County Cork- Pay raise
Ad- All disciplines such as product handling, ESD Practices, machine operations, safety at work etc must be observed.
- Tekno Surgical IREDublin, County Dublin
- Coordinate medical device product delivery into hospital sites and ensure that all customers’ requirements are met.
Technical Writer
Job details
Full job description
Technical Writer
Location: Limerick
Duration: 12 Months
Hours: 39 hours
To provide technical writing, documentation coordination and project support for the Maximo implementation, ensuring that deliverables associated with spare parts, asset register development, preventive maintenance, systems integration, IT, Quality, compliance and system readiness are accurate, consistent, traceable and completed in accordance with applicable Johnson & Johnson Quality Policies, procedures and project governance requirements. The role will collaborate with Asset Care & Reliability, Engineering, Maintenance, Quality, Operations, IT, Supply Chain, Procurement and relevant subject matter experts to support the controlled development, review, approval and release of Maximo project documentation and data.
Roles and Responsibilities
-
Excellent technical writing, editing, proofreading and information-structuring capability, with strong attention to detail.
-
Ability to understand complex engineering, maintenance, Quality and business processes and translate them into clear documents for different user groups.
-
Expertise in Microsoft Word, Excel and PowerPoint, including document formatting, data review, trackers and controlled templates.
-
Experience with electronic document management and Quality systems; familiarity with SharePoint or similar collaborative document repositories is desirable.
-
Experience with a computerized maintenance management system or enterprise asset management platform; Maximo experience is strongly desirable.
-
Working knowledge of asset master data, spare-parts data, preventive maintenance, maintenance processes, asset hierarchies and data governance is desirable.
-
Ability to understand and document system integrations, data flows, interface requirements, field mappings, testing activities and IT support processes.
-
Excellent verbal communication, stakeholder engagement, customer service and cross-functional collaboration skills.
-
Ability to manage multiple documents and priorities, work independently, meet deadlines and escalate risks or gaps promptly.
-
Self-starter who establishes priorities, maintains accurate trackers and drives assigned documentation through review and approval.
-
Ability to build effective working relationships with Engineering, Maintenance, Quality, Operations, IT, Supply Chain, Procurement and external vendors.
How to Succeed
-
Qualification in an appropriate discipline such as Engineering, Maintenance/Reliability, Information Systems, Technical Communication, Life Science or a related technical field, or equivalent relevant experience.
-
Experience producing or managing technical documentation in a regulated, engineering, manufacturing or maintenance environment.
-
Understanding of document control, change control, traceability, data integrity and formal review and approval processes.
-
Understanding of GMP, compliance, validation practices, system development life cycle principles and regulatory expectations relevant to a medical-device environment.
-
Working knowledge of applicable medical-device Quality and electronic-record requirements, including 21 CFR Part 820 and 21 CFR Part 11, as relevant to assigned activities.
Benefits
This role offers a very competitive hourly rate. This contract will run for 12 months.
about Johnson & Johnson Vision
Johnson & Johnson Vision brings together cutting-edge insights, science, technology and people. We partner with eye care professionals and help more people around the world preserve and restore sight. Our portfolio includes the best selling contact lens brand in the world, ACUVUE®, plus consumer eye health solutions, dry eye treatments, refractive (Lasik) and cataract products. Contribute to the next healthcare breakthrough, create a world connected by SIGHT™ with your next project at Johnson & Johnson Vision.
https://jnjvisionpro.co.uk/
Application Process
We are looking to process the first round of applications within the next 2 working days.
We do not accept applications via email. The pay rate for this role will depend on how you are paid. PAYE, LTD & Umbrella options are available.
Diversity, Equity & Inclusion
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.