McDermott Laboratories Limited Posted September 28, 2026

Device Equipment Engineer

Northern Cross, Ireland Full time
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McDermott Laboratories Limited is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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.

The Device Equipment Engineer will act as the technical owner for assigned equipment workstreams, responsible for supporting specification development, supplier engagement, commissioning, qualification and transfer activities from concept through implementation. Working closely with suppliers, CMOs and cross-functional stakeholders, the successful candidate will execute equipment projects in support of GDD program delivery, ensuring solutions meet specification, quality and timeline requirements.

This global role provides exposure to the full product lifecycle, from development through commercialization, while offering an opportunity to develop advanced technical, project execution and leadership skills within the engineering organization.

Every day, we rise to the challenge to make a difference and here’s how the Device Equipment Engineer role will make an impact:

Key responsibilities for this role include:

Provide Equipment ownership from specification development through delivery, commissioning, qualification and transfer to manufacturing, including equipment specification development and supplier interactions for device program activities.

Support engineering projects through the development, specification, procurement, commissioning, qualification and transfer of manufacturing equipment and associated systems.

Develop and implement engineering solutions that meet product and process requirements across device programs, including manufacturing processes, equipment specifications and automation solutions supporting product performance and quality requirements.

Execute equipment and process development, characterization and testing activities, including process development, process characterization, scale-up and technology transfer activities.

Execute and own equipment commissioning, qualification and verification activities, including URS, DQ, FMEA, IQ, OQ, PQ, FAT and SAT, from specification through implementation and transfer to manufacturing.

Lead technical project execution activities associated with external suppliers, equipment manufacturers, Viatris affiliates and CMOs, including assembly, label and pack, supplier and CMO meetings, equipment reviews and project milestones.

Participate in and support cross-functional project teams, working with manufacturing, quality, validation, supply chain and site engineering teams to execute engineering systems objectives in line with program delivery plans.

Provide technical input and engineering documentation, including technical reviews, engineering reports, specifications, protocols, risk assessments, change controls and engineering assessments, together with accurate engineering reporting and project status updates.

Support engineering risk assessments, troubleshooting and investigations, including equipment and manufacturing process issues, change control impact assessments, problem-solving activities, risk management and mitigation, process control alignment and mitigation activities.

Support technology transfer, site integration and lifecycle activities, including coordination with site engineering teams, technical support to manufacturing sites and external partners, and continuous improvement of quality system processes associated with device development and lifecycle management.

Support engineering operations and continuous improvement, including budget forecasting, invoice management, purchase order generation, Work Orders and CDAs, data analysis and performance monitoring, while developing technical and project management competencies through increasingly complex engineering projects and cross-functional collaboration.

The minimum qualifications for this role are: 

Degree in Engineering, Science or equivalent technical discipline.

3 – 5 years' experience in pharmaceutical, medical device, combination product, automation or related engineering environments.

Demonstrated experience supporting engineering projects and equipment implementation activities.

Strong technical documentation and report writing skills within a regulated environment.

Strong communication skills and ability to work effectively within cross-functional teams.

Enthusiastic, motivated and self-directed approach to problem solving.

Attention to detail and systematic approach to execution of engineering activities.

Desirable to have experience working with equipment suppliers, CMOs or contract engineering organizations.

Familiarity with packaging development, transport trays and associated testing activities.

Familiarity with AutoDesk, Microsoft Project, or similar engineering tools.

Experience supporting medical device, combination product or pharmaceutical development projects.

Familiarity with GAMP5 principles.

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.

A t Viatris, we offer   competitive   salar ies , 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.

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Northern Cross, Ireland
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 3753 comparable Manufacturing & CMC roles across 173 biopharma companies.

3753Comparable roles tracked
3372Currently active
173Companies hiring similar roles
64Countries represented

Salary context

921 of 3753 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Biologics Support Operator I (3rd Shift) · AbbVie $14/hr – $26/hr (≈ $29,099–$54,122/yr)
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $41,610 – $381,150 (median $125,550)

Where these roles are based

Top locations among the 3753 comparable roles

United States1739
Germany251
India166
France146
Ireland136
China123

+ 58 more countries

Seniority mix

1670 of 3753 peers have a known seniority level

Senior431
Manager381
Intern/Fellow/Postdoc259
Associate162
Principal138
Associate Director119
Director115
Senior Director57
Executive/VP8

Therapeutic area mix

24 of 3753 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease15
Rare Disease3
Oncology3
Respiratory1
Dermatology & Aesthetics1
Immunology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
McDermott Laboratories Limited Northern Cross, Ireland Director
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland Senior
Same function Same country
40%similar
McDermott Laboratories Limited Northern Cross, Ireland
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland Director
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Director, Combination Product Development
McDermott Laboratories Limited · Northern Cross, Ireland · Director
Function Therapeutic area Seniority Country
40%
Senior Process Engineer
Mylan Teoranta · Inverin, Ireland · Senior
Function Therapeutic area Seniority Country
40%
Associate Biotech Production Specialist
Regeneron Ireland · Limerick, Ireland · Associate
Function Therapeutic area Seniority Country
40%
Sr. Automation Engineer - Packaging
Amgen Technology (Ireland) UC · Dun Laoghaire, Ireland · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.