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88 Jobs Found 

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Senior Embedded Engineer (C++) - R&D Medical Devices - Dublin South

ITSearch

Dublin, Dublin
11 days ago
Dublin, Dublin
11 days ago

Senior Embedded Engineer (C++) - R&D Medical Devices - Dublin South

 

My client based in Dublin South is a world leading firm in the area of wearable technology and has engaged IT Search to speak to candidates regarding this challenging senior role that will work within R&D to create complex medical devices.

 

The role is to join an existing global team headquartered here as a Senior team member, mentoring more junior staff but bringing significant expertise to the R&D team in the areas of designing, testing and implementing embedded processes at all levels of the architecture. Working within compliance and regulatory guidelines, this role will allow the Senior Engineer to produce cutting edge technological solutions to the medical community.

 

This will be a hybrid onsite/remote role so candidates will need to be based within a commuting distance.

 

Candidates should have:

  • 10+ years of commercial development experience using Embedded C++ post graduation, ideally within a pharmaceutical or highly regulated environment
  • Microcontroller expertise alongside Assembly, RTOS and debugging
  • Exceptional communications skills, able to work with multiple areas of the business and various locations and have a track record of strong documentation

 

To learn more about the role, client and process, please forward your CV stating required salary and availability and we can arrange a discussion.

 

Please note, we can only accept applications from candidates eligible to work in the EU

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Senior QA Specialist (Combination Product)

Tandem Project Management

Dublin, Dublin
3 days ago
Dublin, Dublin
3 days ago

Summary:
A QA Specialist for Medical Device Combination Product is required for a biotech in West Dublin. The successful candidate will provide quality oversight and support for clinical and commercial devices and combination products from introduction throughout the product and design control lifecycle and the associated Quality System. As a significant quality contributor, the incumbent will proactively engage with all stakeholders involved with supplier quality agreements, device and combination product batch release, risk management and QMS audit preparation during technology transfer and commercial operations.
Responsibilities:

  • Responsible for documenting and periodic review of supplier quality requirements and supplier quality agreements.
  • Responsible for the review and approval of batch release for combination products.
  • Ability to identify non-conforming batch results or trends and escalate them via the Quality Management System.
  • Support risk assessments relating to batch release or product quality for clinical and commercial products.
  • Ensure timely entry, processing, and closure of quality records in compliance with procedures.
  • Support the review of Design Control deliverables including Risk Management activities.
  • Responsible for coordination & documentation of the Change Control Review Board for Medical Device Changes.
  • Support the development of the QMS as it pertains to Medical Devices and Combination Products to achieve the ISO 13485 standard and compliance with 21CFRPart4 and the medical device regulation 2017/745.
  • This will involve supporting quality input to the implementation to the QMS, reviewing new SOPs, mock audits, internal audits and updates to SOPs.
  • Support internal audit activity from coordination, preparation and execution to improve the QMS and support stakeholders in adherence to the QMS.
  • Supports Notified Body and Health Authority inspections and compliance.

Qualifications & Experience:

  • Minimum of a B.Sc. degree in biological /chemical sciences, biomedical/mechanical engineering, or other related subject.
  • Minimum of 4+ years’ experience in Quality with medical device or combination products in a regulated environment.
  • Risk Management Standard for Medical Devices ISO 14971 2019.
  • Knowledge of the regulatory and compliance requirements of design control for medical devices and/or combination products (e.g. FDA QSR 21 CFR Part 4 and 820 / ISO 13485 and Regulation (EU) 2017/745).
  • Familiarity with SAP and Trackwise would be desirable.
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Inside Sales Account Manager - French speaker

Cardinal Health

Leopardstown, Dublin 18
24 days ago
Leopardstown, Dublin 18
24 days ago

Inside Sales Account Manager

At Cardinal Health, we aim to be a trusted partner, offering a broad range of innovative solutions that help our customers provide cost-efficient, more effective healthcare. Join our team of 50,000 humble partners striving each day to make healthcare more efficient, providers more effective, and patients as healthy as possible.

We are currently looking to recruit an Inside Sales Account Manager to serve our customers in Northern France. This role is based in our Dublin office in Ireland. Reporting to the inside Sales Manager you will be responsible for, but not limited to, the following.

Essential Duties and Responsibilities

  • Experienced in remote selling techniques

  • Translates the results of market insights into a clear prioritization of sales actions

  • Identify target accounts, opportunities and customer priorities

  • Account planning including identify & advance relationships with key stakeholders and decision makers

  • Promotes assigned product portfolio with best practice clinical or non-clinical evaluation, demonstrations and product trainings

  • Leads price and contract negotiations to successfully close customer deals

  • Market & Business Intelligence: Works proactively and in a structured way on market analytics and market research around customers, competitors and general market trends

  • Conducts regular business reviews with customers and internal stakeholders

  • Ensures repeat purchase orders by understanding customer buying decisions making process & patterns

  • Communicates & aligns on a regular basis with field sales force and local Marketing organization of our Medical Solutions business

  • Collaborates tender & contract departments on managing large scale tender and / or contract sales cycle of accounts

  • Improve tender submission quality by preparing high quality supporting documents

  • Closely collaborates with Customer Service, Commercial Operations and Field Sales Team

  • Fully utilizes all available sales tool to maximize sales efficiency (SFDC) and completes all required administrative tasks (call reports and other KPI and metrics reports)

  • Travel Required: Occasional travel (max up to 20%) to selected accounts in country required

Competencies

  • Understands the business: understands customer priorities, market trends & opportunities

  • Analyses issues: Strong analytical thinker with a great ability to think through issues in a structured way, develops insights and is able to drive quality decisions out of analysis

  • Collaborates with others: is a trustworthy individual who is able to build a strong internal & external network of stakeholders remotely and who is capable of working with a number of internal and external stakeholders on reaching defined business goals

  • Understands the impact on patients & customers: Knows customers and the patients connected to them, understand their evolving needs and puts the customer & patient at the centre of his/her work focus

  • Generates ideas: Thinks in innovative ways and pursues new ideas that create meaningful innovations & solutions for customers. Is competent & confident with new technology (systems & programs)

  • Enables operational excellence: Proactively identifies improvements for personal efficiency and focuses on continuous improvement, has a strong orientation to detail to deliver high quality results

  • Strong negotiation skills & ability to close deals with customers

  • Strong presentation / communication skills over the phone

Qualifications & Experience

  • B.A degree in a relevant discipline would be desirable

  • Fluency in French and English language is essential

  • 1 - 3 years of sales experience, ideally in Medical Devices or Tech.

  • Optionally field sales experience OR customer service experience in the Medical Devices/Pharmaceutical/Healthcare industry

The Company

Headquartered in Dublin, Ohio, Cardinal Health (NYSE: CAH) is a health care services company that improves the cost-effectiveness of healthcare. As the business behind healthcare, Cardinal Health helps pharmacies, hospitals and ambulatory care sites focus on patient care while reducing costs, improving efficiency and quality, and increasing profitability. Cardinal Health is an essential link in the healthcare supply chain, providing pharmaceuticals and medical products to more than 100,000 locations each day and is also the industry-leading direct-to-home medical supplies distributor. The company is a leading manufacturer of medical and surgical products, including gloves, surgical apparel and fluid management products. In addition, the company supports the growing diagnostic industry by supplying medical products to clinical laboratories and operating the nation's largest network of radio pharmacies that dispense products to aid in the early diagnosis and treatment of disease. Ranked #14 on the Fortune 500, Cardinal Health employs more than 50,000 people worldwide. More information about the company may be found at www.cardinalhealth.com

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Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.

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QA Specialist - MDR Project

Clarity Life Science

Dublin, Dublin
30+ days ago
Dublin, Dublin
30+ days ago
Clarity Life Science is excited to propose this pharmaceutical job. Our client, a global pharmaceutical company with commercial operations in more than 100 countries, is looking to employ a Quality Assurance Specialist on a 12 months, full-time contract.
Given the recent changes in the Medical Device Regulation (MDR), the QA Specialist will have the responsibility to provide support during the transition period that is ending in May 2020.
Your responsibilities: 
In this position, you will mainly support the implementation of the Economic Operator MDR for the global supply chain. 
  • Ensure the vendors (manufacturers, distributors or other third party companies) have their Technical Agreements updated. 
  • Support the Quality System Management to ensure the changes are aligned to the project and the other QMS tools.
  • Support and document during the investigation of any non-conformance (Deviation Management System - CAPAs).
  • Design, develop and implement Key Performance Indicators within the Quality Assurance area to align with company and global quality objectives.
  • Implication in the design and the generation of the verification process for EO sampling and attest of their compliance. 
  • Excellent collaboration with the QA team onsite, they’ll also be there to support.
  • Ensure alignment in all the SOP’s related to the EO processes. Review and update them accordingly. 
  • Other elements of the MDR project as required.
What you ideally have:
  • Ideally a level 7 Degree in a medical/scientific related field.
  • Minimum 3 years’ experience in quality related or production in the pharmaceutical or medical device industry.
  • Knowledge of the Quality System required for pharmaceutical and/or medical device industry.
  • Previous documentation experience, ideally in a pharmaceutical or medical device company. 
The skills you have: 
  • Enthusiasm and oriented towards Quality improvement.
  • Excellent project management and administrative skills with good proficiency in Word, Excel and PowerPoint. 
  • Excellent collaboration within the team but ability to manage own workload without supervision. 
  • Manage the workload with flexibility in responding to urgent requests and operate according to agreed performance standards such as timelines.

To discuss this pharmaceutical job in greater detail please contact Marc on +353 (0)1 963 1370 - marc@claritylifescience.com or by submitting your CV. All queries and applications are fully confidential.
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Medical Writer/Senior Medical Writer

Fishawack Health

Dublin
10 days ago
Dublin
10 days ago

Salary: Competitive (dependent on experience) excellent benefits

Location: Ireland, fully remote 

About the role

A Fishawack Medical Writer researches, writes, edits and prepares high-quality material for a variety of customised medical communications initiatives. A keen interest in medical science and writing, coupled with an ability to work to strict deadlines and specifications is essential.

Who are Fishawack Health?

Fishawack Health is the leading global commercialisation partner for the life science industry. Established in 2001 and headquartered in the UK, Fishawack Health is now an 800 strong global organisation, bringing together best-in-class agencies and experts across Medical Communications, Consulting, and Commercial.

We help develop, launch, and grow brands for clients across the life sciences industry, including global pharmaceutical and medical device manufacturers and emerging biotech and healthcare companies. Our internationally registered, award-winning teams collaborate across operations in the UK (Knutsford, Manchester, Brighton and Oxford) and USA (Evansville, New York, Philadelphia, Scottsdale, St. Louis and San Diego).

What you'll do

 As a Medical Writer you will be responsible for developing and delivering original, accurate, high-quality content (manuscripts, slides, and other editorial assignments) within the project specifications, timeline, and budget. This will involve:

  • Liaising with clients, authors and colleagues to progress projects effectively,
  • Attending congresses, symposia and advisory board meetings as required and liaising with speakers and clients
  • Providing input on project specifications, costings and schedules, working with the internal account team to ensure projects are delivered to time and budget
  • Providing good briefings to colleagues and freelancers
  • Actively participating in account development meetings to grow repeat business
  • Mentoring new writers (depending on individual, level of experience and opportunity)

About you

  • Bachelor’s degree in the life sciences required; post-graduate qualification e.g. MSc, MPhil or PhD an advantage
  • Previous experience in medical writing/publishing role and/or medical communications agency environment advantageous
  • Proficiency in the use of MS Office, specifically Word, PowerPoint, and Excel
  • Proficiency in Internet and PubMed searches
  • Ability to work independently with minimal supervision, and as part of a team

What we offer 

We offer a creative, supportive environment with a uniquely diverse career structure where you will be able to continuously develop. Our STEPS training programme – Supporting Training, Enhancing Professional Development – provides a broad range of training delivered in-house and on-line, and supplements on-the-job training/project team-led training initiative, amongst other benefits.

Reasonable adjustments: We'll consider any reasonable adjustments you'd like us to put in place in the interests of fairness and equal opportunities.

We encourage all applicants to read our company Privacy Policy before applying to a role.

Powered by JazzHR

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Scientific Director / Senior Scientific Director - Medical Communications

Fishawack Health

Dublin
3 days ago
Dublin
3 days ago

Salary: £Competitive excellent benefits (bonus, healthcare, pension, life cover etc.) 

Location: Ireland, fully remote 

About the role 

As a Scientific Director/Senior Scientific Director you will be a scientific expert, providing insights and knowledge to projects, clients and new business efforts. You will review projects for strategic alignment and scientific accuracy, and when needed, act as the medical writer for more scientifically complex projects. Acting as a client relationship manager, you will build scientific credibility and partnerships, ensuring a high level of service with each client. You will provide scientific and strategic expertise to new business development activities, researching and developing content for pitches, as well as being part of the presentation team. Building a support network for junior members of the team, you will work closely with medical writers, account teams, client services and project management. In return, Fishawack will offer you excellent job benefits, on-going career opportunities and a supportive & flexible working environment.

Who are Fishawack Health? 

Fishawack Health is the leading global commercialisation partner for the modern life sciences era. Powered by a globe-spanning pack of strategic, creative, and scientific experts, we are driven to connect patients and healthcare professionals with the knowledge they need to live better lives.

Our three core operating units—Commercial, Consulting, and Medical Communications—can be leveraged individually but are designed for dynamic collaboration, with expert teams intentionally and uniquely assembled for each project. By bringing together best-in-class capabilities from around the world, we empower our clients—global pharmaceutical, medical device manufacturers, and emerging biotech and healthcare companies—to navigate the most complex of ecosystems while embarking on a faster, more efficient path to developing, launching, and growing their brands and portfolios.

Our internationally recognised, award-winning teams collaborate across operations in the UK (Brighton, London, Manchester, Knutsford, Dublin and Oxford) and USA (Evansville, New York, Philadelphia, Minneapolis, Scottsdale, St. Louis, and San Diego).

What you'll do

  • Work closely with teams, leading the scientific development of projects
  • Lead the development of scientifically complex materials as appropriate, proactively driving projects through to completion
  • Combine in-depth scientific understanding of the product/therapy area with strong commercial awareness to inform all deliverables and communication planning recommendations
  • Build and maintain relationships with clients, ensuring the highest level of service
  • Participate in business development activities, such as pitching and proposals
  • Provide leadership to ensure that teams are exceeding performance standards and developing professionally

About you 

  • 5-10 years' experience in a medical communications agency environment, including medical writing experience and editorial management experience
  • Bachelors degree in the life sciences; PharmD or PhD highly preferred
  • Proficiency in the use of MS office, PowerPoint and Excel

What we offer 

We offer a creative, supportive environment with a uniquely diverse career structure where you will be able to continuously develop and tailor your career towards your preferred route, be that scientific delivery, operational, or client service. Our STEPS training programme – Supporting Training, Enhancing Professional Development – provides a broad range of training delivered in-house and on-line, and supplements on-the-job training/project team-led training initiatives. We also offer a generous company pension, private medical insurance plus many other excellent employee benefits.

We encourage all applicants to read our company Privacy Policy before applying to a role.

Powered by JazzHR

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GP Medical Receptionist

Osborne

Dublin, Dublin
1 day ago
Dublin, Dublin
1 day ago

Introduction

€13- €15 per hour

Onsite Parking

4.5 Day Week

Duties & Responsibilities:

  • First point of contact for Meet / Greet Patients (In person & by phone)
  • Scheduling appointments, and maintaining Patient records and accounts.
  • Filing and retrieving patient records.
  • Maintain patient accounts by obtaining, recording, and updating personal and finance
  • Collecting & Recording patient charges.
  • Stock check to determine inventory level, anticipating needed supplies, placing orders for supplies, verifying receipt of supplies.
  • Scheduling equipment service and repairs.
  • Empathy towards patients in distress & respond to Emergency
  • Protect patients’ rights by maintaining confidentiality of medical, personal, and financial information.
  • All other Adhoc Administration duties

 

Essential Requirements

  • GP Practice Reception / Admin experience is absolutely essential
  • Strong Communications
  • Proficient using MS Office Suite (outlook, word, excel etc)
  • Proficient with 1 or more GP Software
  • Flexibility when it comes to daily task 
  • High level of accuracy & attention to detail.

 

For more information please apply through the link provided for the attention of Karen O'Rourke or call Osborne Recruitment on 01 598 4334

If you are interested in finding out more about the above role and would like to be considered other suitable roles that we may have available for your skill set - please attach your CV via the link provided

Please submit your updated CV in Word Format

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Engineering Manager

BD

Dun Laoghaire
3 days ago
Dun Laoghaire
3 days ago

Job Description Summary

BD, also known as Becton Dickinson, provides pen needles for the care of Diabetes patients globally. The plant, based in Dun Laoghaire, runs 24/7 and is the Worldwide Centre of Excellence for Pen Needle Manufacturing within the BD organisation, producing 4.6 billion medical devices annually. Here we employ approximately 450 people across Operations, Engineering, Quality and R&D.
The Engineering Manager is responsible for the management, direction and coordination of all engineering activities at the Dun Laoghaire plant.
You will manage facilities, sustainability, new product introductions and product/process development.
You will work with the Worldwide Director of Engineering to ensure alignment of priorities associated with New Product Introductions and Technology / Process changes.

Job Description

  • Provide consistent leadership and direction to engineering function within Dun Laoghaire plant. You will manage facilities, sustainability, new product introductions and product/process development
  • Develop a team of direct reports and ensure that a succession pipeline identified and implemented
  • Manage new product introduction and product/ process development across the plant.
  • Overall responsibility for implementing capital expenditure projects across the plant.
  • Manage capital spend tracking, monthly reporting and forecasting.
  • You will lead the Plant Priority Matrix ‘PPM’ process and interface with project owners to ensure projects are on track and communicate any roadblocks with suggested solutions to site leadership.
  • Working with procurement and global real estate & construction to ensure that all projects are executing in line with BD procedures.
  • Drive key changes and continuous improvement in site engineering systems and procedures.
  • Manage Key Cost to Win programs and ensure that projects are rolled out as required.
  • Liaise on a worldwide basis with BD Engineering, Quality, R&D, Marketing and Manufacturing staff.
  • Maintain the environmental and IPC licence compliance. 
  • Any other reasonable duties which may be required by management from time to time

  • Relevant Experience:
  • A minimum of 8 years’ experience in engineering leadership environment with at least 5 years at a senior management level, ideally within a Medical Devices/Pharmaceutical Industry.
  • Strong leadership skills with a proven track record of success in leading a large engineering function.
  • Proven ability to influence and effectively manage high demands in an environment with limited resources
  • Agile learner, excellent interpersonal skills and results obtained.

Why join us?

A career at BD means that you are part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here you can fulfill your life’s purpose through the work that you do every day.

You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program — which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components — is designed to support the varying needs of our diverse and global associates.

To learn more about BD visit https://emea.jobs.bd.com/

Primary Work Location

IRL Dun Laoghaire - Pottery Road

Additional Locations

Work Shift

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Qualified Person - Quality

Teva Pharmaceuticals

Baldoyle
14 days ago
Baldoyle
14 days ago
Qualified Person - Quality
Date: Feb 10, 2021
Location: Baldoyle, IE, D13
Company: Teva Pharmaceuticals
Who are we?
We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. Yet until today, you may not have heard of us.
We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world.
We would like to invite applications for the role of Qualified Person (QP) at our Baldoyle site. As Qualified person, you will perform key Quality responsibilities with respect to certification of batches of medical products prior to release for sale or distribution, including Medicinally Licensed over the Counter products as well as third party manufactured medicinal products
The role will also provide release support for cosmetics and Medical Devices as required, staying current with proposed and implemented regulations, and understanding industry trends. As QP you will Interface and collaborate with corporate and functional area management to ensure systems utilised for quality oversight and management are compliant and consistent with Teva Corporate standards to maintain the site’s inspection readiness status
A day in the life of our Qualified person
+ Act as Qualified Person for release of products in accordance with article 51, EC directive 2001/83/EC
+ Act as QP representative for regulatory inspections where necessary. Where appropriate ensure all relevant manufacturing licenses are maintained
+ Participate in Continuous Professional Development (CPD) initiatives with a view to maintaining, developing and broadening knowledge and skills as they relate to the function of Qualified Person. (Including presentations, tutoring, workshops, self-learning, reading, formal academic education etc.)
+ Review deviation reports including all associated CAPA’s and investigations ensuring that any deviations or planned changes with a potential to impact the product have been authorized
+ Participation of deviation investigation where deemed appropriate
+ Ensure any changes requiring variation to the manufacturing authorisations (MIA) have been notified and authorized by the relevant authority
+ Ensure each batch certified and its manufacture complies with the provisions of the marketing authorisation. Ensure all necessary checks and tests are adequate and performed correctly
+ Maintain a register (or equivalent document) as a record of product batches certified by the Qualified Person prior to release
+ Conduct external audits of vendors, contract laboratories and contract manufacturers as appropriate
+ Conduct internal audits of various departments as appropriate to support Inspection readiness
+ Participate in regulatory, corporate and customer audits of sites when required
Who are we looking for?
Are you ….
• Qualified Pharmacist or Graduate of Diploma in Pharmaceutical Manufacturing Technology or equivalent “Qualified Person” status as defined by E.C. Directive 2001/83
Do you have….
+ Proven experience within the Pharmaceutical industry in a leading QA/QC/Compliance role.Broad Knowledge of Analytical Techniques and Experience in HPLC
+ Excellent knowledge of regulations and sources of regulatory information.
+ Experience of creams and ointments manufacture would be an advantage
+ Understanding of Production and Laboratory systems to effect judgement decisions consistent with business needs.
+ Strong Team Building and Communication skills
+ Excellent planning and organisational skills to ensure workload prioritisation and schedule adherence.
+ An understanding of internal/external customer requirements and an ability to respond promptly to needs.
+ Ability to work on own initiative to meet and exceed business objectives
Function
Quality
Sub Function
Quality Assurance Methods
Reports To
Head of Quality
Already Working @TEVA?
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:Internal Career Site (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
Teva’s Equal Employment Opportunity Commitment
At Teva, we pride ourselves on being a company where we can all thrive, and where everyone feels comfortable being their true self.
Diversity and inclusion sits at the heart of everything we do. By valuing difference, we can be a better employer for our colleagues, and provide a better service for our customers and patients. That’s why we’re constantly looking for ways in which we can learn from each other, embrace what makes us unique and contribute to a fairer society free from discrimination and prejudice
EOE including disability/veteran

Job Type

Full Time

Posted

11 days ago

Description

Senior Embedded Engineer (C++) - R&D Medical Devices - Dublin South

 

My client based in Dublin South is a world leading firm in the area of wearable technology and has engaged IT Search to speak to candidates regarding this challenging senior role that will work within R&D to create complex medical devices.

 

The role is to join an existing global team headquartered here as a Senior team member, mentoring more junior staff but bringing significant expertise to the R&D team in the areas of designing, testing and implementing embedded processes at all levels of the architecture. Working within compliance and regulatory guidelines, this role will allow the Senior Engineer to produce cutting edge technological solutions to the medical community.

 

This will be a hybrid onsite/remote role so candidates will need to be based within a commuting distance.

 

Candidates should have:

  • 10+ years of commercial development experience using Embedded C++ post graduation, ideally within a pharmaceutical or highly regulated environment
  • Microcontroller expertise alongside Assembly, RTOS and debugging
  • Exceptional communications skills, able to work with multiple areas of the business and various locations and have a track record of strong documentation

 

To learn more about the role, client and process, please forward your CV stating required salary and availability and we can arrange a discussion.

 

Please note, we can only accept applications from candidates eligible to work in the EU