Viatris Logo

Viatris

Scientist, Device and Product Performance

Posted Yesterday
Be an Early Applicant
In-Office
North Hill, Dublin
Junior
In-Office
North Hill, Dublin
Junior
The Scientist will provide technical expertise in developing Combination Products, conduct various tests, ensure compliance with regulations, and support documentation and lab activities.
The summary above was generated by AI
McDermott Laboratories Limited

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.
Viatris empowers people worldwide to live healthier at every stage of life.
We do so via: 
Access – Providing high quality trusted medicines regardless of geography or circumstance;
Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and 
Partnership – Leveraging our collective expertise to connect people to products and services. 
 

Our Global Device Development is an innovative, technically-excellent and fully integrated organization, delivering access to high quality, safe, robust and effective device and combination products to meet the worlds’ evolving patient healthcare needs. We develop device technologies to enable drug-delivery for respiratory, biologic, biosimilar and injectable products, and work across Viatris to support innovative technology solutions to provide healthcare solutions for our patients. We operate from 4 sites: Dublin, Ireland, Cambridge & Sandwich, UK and Southpointe, Pittsburgh, USA. Every member of our team is dedicated to creating better health for a better world, one person at a time. 

 

Every day, we rise to the challenge to make a difference and here’s how the Scientist/Engineer (Device and Product Performance), will make an impact 

 

Key responsibilities for this role include: 

  • Provision of technical expertise to support the development of Combination Products. 

  • Responsible for activities such as metrology testing, engineering verification, design verification, device functional stability, biological evaluation, method development, transport & shipping studies. 

  • Performing Development and Validation of Test Methods to support Design Verification Testing either to internal/external test facilities or manufacturing sites. 

  • Dealing with Viatris Affiliates and/or Third Partner Companies to support exhibit and registration batches, through review and implementation of controls and additional requirements if needed such as manufacturing investigations. 

  • Responsible for testing of combination products within the Global Device Development portfolio including generation of protocols, oversight of execution of testing at external test facilities and writing of reports. 

  • Trending and statistical analysis of analytical data including compilation of technical reports to support combination product development lifecycle. 

  • Ensuring that the Combination Product meets any requirements for reliability, through implementation of appropriate controls and assessment of the product against suitable specifications. 

  • Responsible for compilation and review of technical documentation within GDD in line with global regulatory requirements, guidance’s and the latest regulatory and industry thinking. 

  • Support of all R&D Lab activities including, Equipment calibration and Qualification, Documentation requirements, Trackwise records. 

  • Attending EHS training and maintaining responsibility for adhering to appropriate EHS procedures. Ensure the appropriate risk assessments are in place to perform required tasks. 

  • Support equipment qualifications, vendor calibrations and preventative maintenance in line with the laboratory qualification and preventative maintenance schedule as required. 

  • Lead general laboratory activities including; Procedure updates, generation of metrics, sample management, data review/ verification, instrument daily calibrations, shipping of samples. 

 

Responsible for following all EHS process and procedures 

The minimum qualifications for this role are:  

  • Degree in Science/Engineering (Master’s preferred) 

  • Proven experience in pharmaceutical and/or medical device development 

  • Experience in the development and validation of analytical methods 

  • Experienced in application of statistical techniques for data analysis. 

  • Working knowledge of design control requirements in line with FDA 21 CFR part 820 and ISO 13485 would be an advantage 

  • Experience of writing and supporting regulatory submissions would be an advantage 

  • Highly driven and motivated person who can work as part of a flexible, dynamic team whilst taking responsibility for individual tasks 

  • Well-developed communication skills to lead or facilitate effective discussions. Able to communicate technical and/or project information to key stakeholders. 

  • Some travel will be required as part of this role. 

 

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.  

 

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. 

Viatris is an Equal Opportunity Employer.

Top Skills

Fda 21 Cfr Part 820
Iso 13485
Statistical Techniques For Data Analysis

Viatris Dublin, Dublin, IRL Office

Dublin, Dublin, Ireland

Similar Jobs

Yesterday
In-Office
North Hill, Dublin, IRL
Entry level
Entry level
Healthtech • Biotech • Pharmaceutical
Support R&D lab activities, execute inspections, validate test methods, analyze data, and adhere to ISO 13485 in a regulated environment.
Top Skills: MinitabTrackwise
Yesterday
In-Office
North Hill, Dublin, IRL
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical
Lead a team to design verification strategies, develop specifications, and provide expertise in combination product development ensuring alignment of drug and device teams.
Top Skills: Fda 21 Cfr Part 820Iso 13485Statistical Techniques
8 Days Ago
In-Office
2 Locations
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical
Lead and support the development of combination products, ensuring alignment between drug and device teams, and conducting design verification and reliability testing.
Top Skills: Analytical MethodsFda 21 Cfr Part 820Iso 13485Statistical Analysis

What you need to know about the Dublin Tech Scene

From Bono and Oscar Wilde to today's tech leaders, Dublin has always attracted trailblazers, with more than 70,000 people working in the city's expanding digital sector. Continuing its legacy of drawing pioneers, the city is advancing rapidly. Ireland is now ranked as one of the top tech clusters in the region and the number one destination for digital companies, with the highest hiring intention of any region across all sectors.

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account