Sr. Validation Specialist

PCI WI LSNE Madison, LLC

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Stamullen, Co. Meath, IRL IRL_City North Until 8/21/2026 3+ years exp H-1B sponsor history First posted January 29, 2026 Last posted January 29, 2026
Job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.


We are PCI. 


Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

   

Main purpose of job:

The role of the Senior Validation Specialist is to implement and execute tasks relating to operational support for product launches, Process, Facility and Equipment Development at PCI Pharma Services sites. 

Main responsibilities:

  • Support the validation effort for all Strategic Projects on site.

  • Ensure all validation activities on site relating to Facility, Equipment and Processes meet the expectations of clients but more specifically meet regulatory requirements (HPRA/ FDA).

  • Prepare, review and or approval of qualification and/or validation documentation (VMPs, specifications, protocols, reports etc.) in relation to instrument, equipment, facilities (including cold stores), utilities, automated systems, manufacturing processes and cleaning processes including FAT, SAT, IQ, OQ, PQ phases in conjunction with program Quality representation.

  • Drive solutions, in conjunction with the appropriate department, to ensure customer related validation problems are communicated and corrective actions are in place and closed in a timely manner. Thorough investigation of Quality and Validation issues using Root Cause Analysis methodology and implementation of robust corrective and preventative actions to prevent recurrence. Support change controls as required.

  • Execute validation activities, with minimal supervision, in conjunction with Technical, Production and Engineering functions.

  • Ensure the strict implementation of validation procedures plus the timely and accurate completion of all validation documentation.

  • Supports the coordination & scheduling of packaging validation activities in alignment with planning & packaging functions.

  • Perform Periodic reviews, revalidations, and continued process verifications on a scheduled basis.

  • Support all Regulatory Inspections, Customer visits and Customer audits on validation related queries as required.

Must Have:

  • Min 3 years' Quality experience

  • Min 2 years' Validation experience

  • Equipment Qualification (IQ, OQ, PQ) – Hands on experience in protocol generations, execution, completion

  • Process Validation (PV) experience

  • New Product Introduction (NPI) - Generation, execution and close out of validation projects

  • Communication Customer/Internal stake holders/Suppliers

  • Experience with deviation, CAPA processes

  • Flexible and able to manage multiple priorities simultaneously

  • Periodic reviews

Desired:

  • Experience with packaging - secondary packaging / blister packaging and high speed / automated lines would be a distinctive advantage for this position.

  • Ability to present risk-based project validation strategy in a clear and concise manner to the Business Unit Planners, Customers and where required, to senior management

  • Decision Making: Identify and understand issues, problems and opportunities whilst providing a viable solution

  • Passion for Results: high energy, maturity, ability to work under pressure and deliver results; get things done (an action-oriented approach)

  • Cleaning Validation (CV)

  • Computer Systems Validation (CSV)

  • Temperature mapping

  • FAT, SAT

#LI-JP1

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

About this role

Summary

Execute validation activities to ensure facility, equipment, and process compliance for pharma products.

Job title

Sr. Validation Specialist

Experience level

3+ years

Minimum experience

3+ years exp

Industry

pharmaceuticals

Location requirements

On-site in Stamullen, Co. Meath, Ireland; no remote work.

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

validationIQOQPQprocess validationdeviationCAPA

Preferred skills

packagingrisk assessmentcleaning validationCSVtemperature mapping

Specializations

validationequipment qualificationprocess validationNPIregulatory compliance
Locations

Structured locations inferred from the posting.

Stamullin, Stamullen, Co. Meath, Ireland

On-site City
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