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Salary
≈ $63k – $144k per year (Estimated)
Location
In office (Galway)
Seniority
Staff · 10+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Sep 24, 2026. First seen by Alion on Sep 24, 2026. Viatris scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Viatris is a global healthcare company headquartered in Canonsburg, Pennsylvania, that makes and sells generic, branded and complex medicines, biosimilars and over-the-counter products. It was formed on 16 November 2020 through the merger of Mylan and Upjohn, the off-patent medicines division of Pfizer, and operates in more than 165 countries; this record covers its Finnish affiliate site, while the job board is the group's global Workday board. Openings span regulatory affairs and CMC directors, pharmacovigilance managers, medical and sales representatives, brand managers and production operators in Europe, the US and Australia.
Mylan Teoranta

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.

For those driven to live their lives with purpose, Viatris helps employees realise their full potential by

creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place

to work. This is a place to make a difference in the world.

The Technical Lead Engineer is responsible for providing technical leadership, engineering support,

and maintenance reliability oversight within a sterile injectable fill finish manufacturing facility. The

role has primary responsibility for ensuring plant inspection readiness across engineering systems,

with particular emphasis on HVAC, clean utilities, facility infrastructure, preventive maintenance

programs, and associated Standard Operating Procedures (SOPs).

The successful candidate will act as the engineering lead for the new product program proposed for

the cartridge filling line while providing technical support for existing syringe and vial filling

operations. The role is responsible for developing and maintaining qualification lifecycle documents,

driving maintenance excellence initiatives, improving equipment reliability, and supporting process

development activities to ensure compliant, safe, and efficient manufacturing operations.

The Technical Lead will work closely with Operations, Quality Assurance, Validation, Maintenance,

Facilities, and external contractors to ensure all systems remain in a sustained state of control and

regulatory compliance.

This role is a critical engineering leadership position responsible for ensuring the reliable, compliant,

and efficient operation of sterile fill finish manufacturing systems while driving engineering

excellence, maintenance reliability, and continuous inspection readiness.

Key Responsibilities

1) Plant Inspection Readiness & Compliance Leadership

2) HVAC & Utilities Systems

3) Maintenance Excellence & Reliability Engineering

4) Cartridge Filling Line Technical Leadership

Plant Inspection Readiness & Compliance Leadership

  • Lead engineering activities to maintain continuous regulatory inspection readiness.
  • Ensure HVAC systems, cleanroom infrastructure, utilities, and process equipment comply with

GMP requirements and site procedures.

  • Drive remediation activities arising from audits, inspections, deviations, CAPAs and technical

investigations.

  • Support regulatory inspections and customer audits as the technical subject matter expert for

facilities and engineering systems.

  • Ensure engineering documentation is maintained in an audit-ready state at all times.
  • Periodically review engineering systems for compliance, risk, and operational effectiveness.

HVAC & Utilities Systems

  • Provide technical leadership and oversight of critical facility systems including:

o HVAC and cleanroom environmental control systems

o Clean Steam systems

o Water for Injection (WFI)

o Purified Water systems

o Compressed gases

o Process chilled water

o Building Management Systems (BMS)

o Environmental monitoring support systems

  • Ensure robust preventative maintenance and reliability strategies are implemented for all GMP

utilities.

  • Drive continuous improvement of utility performance through trend analysis and reliability

programs.

  • Support qualification, requalification and periodic review activities for critical utility systems.

Maintenance Excellence & Reliability Engineering

  • Champion maintenance reliability best practices across all production and utility assets.
  • Develop and optimize preventative maintenance (PM) programs using risk-based and reliability

centered maintenance principles.

  • Lead root cause investigations and implementation of sustainable corrective actions for

equipment failures.

  • Establish & report KPI’s
  • Drive predictive maintenance initiatives where appropriate.
  • Partner with maintenance teams to improve asset lifecycle management and spare parts

strategies.

  • Promote a culture of reliability, ownership, and continuous improvement.

Cartridge Filling Line Technical Leadership

  • Serve as Engineering Lead for the cartridge filling line new process development for next

generation product.

  • Provide technical direction for specifying , troubleshooting, optimization, and lifecycle

management of cartridge filling , dispensing and compounding equipment.

  • Lead equipment performance improvement projects.
  • Support process development, scale-up, and introduction of new products onto the cartridge

manufacturing platform.

  • Coordinate equipment upgrades and implementation of technical improvements.
  • Ensure equipment operates within validated and qualified parameters.

Validation & Qualification Support

  • Lead & Support the development and execution of qualification lifecycle documentation

including: partnering with MS&T department and Cartridge program manager

o User Requirement Specifications (URS)

o Functional Specifications (FS)

o Design Qualification (DQ)

o Installation Qualification (IQ)

o Operational Qualification (OQ)

o Performance Qualification (PQ)

o Traceability matrices

o Engineering assessments

o Periodic review documentation

  • Support commissioning and qualification of new equipment, facility upgrades, and utility

systems.

  • Ensure documentation meets GMP, regulatory, and site requirements.
  • Support validation activities associated with process improvements and change controls.

Syringe & Vial Filling Line Support

  • Provide technical engineering support to existing syringe filling operations.
  • Support reliability and maintenance activities on vial filling lines.
  • Collaborate with dedicated maintenance teams to maximize equipment performance and

availability.

  • Lead technical investigations involving critical process equipment.
  • Support continuous improvement initiatives focused on productivity, quality, and operational

excellence.

Continuous Improvement & Process Development

  • Support process development initiatives to improve manufacturing efficiency and product

quality.

  • Identify opportunities for equipment optimization and process simplification.
  • Lead engineering change control activities.
  • Apply Lean Manufacturing, Six Sigma, and Reliability Engineering principles where appropriate.
  • Participate in capital projects and technology transfer activities.

Leadership Responsibilities

  • Provide technical mentoring and coaching to maintenance technicians and engineers.
  • Act as a key engineering SME across fill finish operations.
  • Foster a culture of safety, compliance, reliability, and continuous improvement.
  • Coordinate engineering activities across multiple functional groups and external vendors.

About Your Skills & Experience

For this role, we’re looking for a candidate who has an effective combination of the following

qualifications, skills and experiences:

Education

  • Bachelor's Degree in Engineering (Mechanical, Electrical, Chemical, Manufacturing,

Pharmaceutical Engineering, or related trades qualification with >10 years Pharma experience)

  • Advanced technical or reliability certifications are desirable.

Experience

  • 10+ years' experience within pharmaceutical, biotechnology, or sterile manufacturing

environments.

  • Extensive experience supporting sterile fill finish operations.
  • Strong experience with:

o HVAC systems in GMP environments

o Clean utilities

o Equipment maintenance programs

o Reliability engineering

o Qualification and validation activities

o Regulatory inspections and audit support

  • Experience supporting cartridge, syringe, or vial filling technologies is highly desirable.

Technical Competencies

  • Sterile manufacturing processes
  • GMP and regulatory compliance
  • HVAC and cleanroom systems
  • Clean utilities and critical facility infrastructure
  • Asset lifecycle management
  • Maintenance reliability methodologies
  • Root Cause Analysis (RCA)
  • Reliability Centered Maintenance (RCM)
  • FMEA and risk management
  • CMMS systems
  • Change control management
  • Qualification and validation lifecycle management
  • Data analysis and performance trending

Key Behaviours

  • Strong technical leadership & excellent problem-solving capability
  • Proactive approach to compliance and reliability
  • Ability to influence cross-functional teams with strong communication and stakeholder

management skills

  • Organized and detail-oriented with a Continuous improvement mindset
  • Results-focused with high accountability

Benefits at Viatris

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. Some of our

benefits include the following on top of a competitive salary:

  • Excellent career progression opportunities
  • Work-life balance initiatives
  • Bonus scheme
  • Health insurance
  • Pension

Diversity & Inclusion at Viatris

At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of

our business can be one of our greatest strengths in redefining healthcare not as it is, but as it

should be. If you would like to know more about what diversity, equity and inclusion means to us,

please visit https://www.viatris.com/en/Careers/Diversity-and-Inclusion

Sustainability at Viatris

Corporate social responsibility is fundamental to the Viatris mission. We work to advance

responsible and sustainable operations and leverage our collective expertise to empower people to

live healthier at every stage of life, recognizing that our actions affect the stakeholders and

communities we serve. To learn more about our efforts, please visit

https://www.viatris.com/en/about-us/corporate-responsibility

At Viatris, we offercompetitivesalaries, benefitsandan 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.

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