Senior Risk Management Engineer / Scientist

Viatris; Dublin; On-site; EUR 70,000 - 90,000; Full time

Benefits offered by this job

Competitive salaries

Benefits package

Inclusive environment

Job summary

Viatris in Dublin is seeking a Senior Risk Management Engineer/Scientist to lead Risk Management processes for combination products and medical devices. This role focuses on compliance with regulations while collaborating with cross-functional teams to enhance product safety.

The ideal candidate will have a degree in a regulated environment, strong problem-solving skills, and relevant industry experience. The position supports personal growth in an inclusive workplace committed to healthcare impact.

Qualifications

• Proven direct experience in a regulated Pharma/Medical Device environment.
• Ability to define, organize, and manage individual and team tasks.
• Demonstrable understanding of Medical Device Risk Management principles.

Responsibilities

• Implement and lead combination product/device Risk Management process.
• Lead the development of Risk Management Files to comply with regulations.
• Collaborate with cross-functional teams to analyze and control risks.

Skills

Risk Management expertise

Effective communication

Problem-solving skills

Attention to detail

Education

Degree in a regulated Pharma/Medical Device/GMP environment

Tools

ISO 14971:2019

ISO 13495

Job description

Overview

McDermott Laboratories Limited

Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases.

We have been included on number of award lists that demonstrate the impact we are making.

Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.

Our Global Device Development organization is an innovative, technically strong, and fully integrated team focused on delivering high-quality, safe, and effective device and combination products to meet evolving patient healthcare needs worldwide. It provides leadership, strategic oversight, direction, support, and hands-on training for medical devices and combination products. Through thorough knowledge, this role will support the establishment, maintenance and remediation of risk management files for combination products and devices under development, on-market or acquired. A key focus of this role shall include critical engagement with on-market stakeholders including Quality, Clinical, and Pharmacovigilance to support the monitoring of product performance and safety.

Every day, we rise to the challenge to make a difference and here’s how the Senior Risk Management Engineer/ Scientist role will make an impact:

Responsibilities

• Be responsible for combination product / device Risk Management (RM) process implementation and thought leadership, to ensure the strategic development of Risk Management Files (RMFs), to meet the intended global business needs, in compliance with relevant regulations, standards, guidance and procedures.
• Lead within the GDD Risk Management function, taking responsibility for developing and delivering subject matter expertise to cross-functional teams across the full device lifecycle, including global regulatory submissions, product launch, and post-market support.
• Seek to identify and lead the implementation of process improvements across GDD’s processes, to ensure high quality, efficient program delivery.
• Within RM group, lead and contribute to, the development of RM principles, and associated processes and procedures, to ensure that GDD operates with the latest RM practices to ensure State of the Art (SOTA).
• Under assigned design and development programs, lead Device Program Teams (DPTs) in the development of Risk Management File deliverables including, but not limited to, Failure Mode Effects Analysis (FMEA), Fault Tree Analysis, Medical Hazard Lists, and clinical trial preparation, against the defined design control / design and development timelines.
• Contribute to regulatory submissions, regulatory responses, and external/ third party audits as required by the organization.
• Assess Risk Management Files (RMFs) against on-market data and apply risk-based thinking to post-market sustaining activities to maintain the RMF’s contemporaneousness.
• Collaborate with Device Development colleagues, Product Quality Oversight, Clinicians and Pharmacovigilance teams, through application of RM throughout the product Life-Cycle process to analyse, evaluate, mitigate and control risks, in line with International Standards, Regulatory requirements and local Quality Management System (QMS).
• Lead and support the assessment of Change Controls (CC), Complaint Investigations, CAPAs and Quality Incidents, as applicable.
• Communicate clearly and in a timely manner to program teams and within the functional line team to ensure potential and theoretical risks are identified and communicated in a constructive and timely manner.
• Maintain detailed awareness and understanding of global risk management requirements for medical devices and drug-device combination products in regions of interest to the Viatris portfolio
• Collaborate as part of “One Team”, with a common purpose of delivering high quality device / combination products, that are safe and effective for users

Minimum qualifications

• Degree with proven direct experience, in a regulated Pharma/Medical Device/ GMP environment.
• A team player willing to support any other organisational needs/activities outside primary expertise to continuously develop the business
• Ability to work independently and with minimal direction
• Ability to define, organize, and manage individual and team tasks
• Excellent communication and collaborative skills to lead or facilitate effective discussions. Able to communicate technical information to key stakeholders.
• Experienced in design and development (ISO 13495 / 21CFR 820.) and Risk Management (ISO 14971:2019)
• Familiarity with new product introduction/ development (NPI)/ NPD) and/ or Lifecycle Management / Sustaining
• Demonstrable ability to execute to program deliverables and timelines
• Strong problem solving and analytical skills
• Detail-orientated without compromising on project timelines
• Demonstrable understanding and application of the fundamental principles of Medical Device Risk Management within the regulatory framework of FDA 21 CFR 820.30 and EUMDR 2017/745
• Demonstrable understanding and application of Design, Use and Manufacture risk-related analysis methodologies, including but not limited to FMEAs, FTAs and Medical Hazard Analysis

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.