Validation Specialist

pciservices; Stamullen; On-site; EUR 42,000 - 64,000; Full time

Job summary

PCI Pharma Services in Stamullen, County Meath, Ireland, seeks a Validation Specialist for a permanent, on-site role. You will implement and execute validation tasks across Process, Facility and Equipment Development, including PV, CV and CSV, ensuring GMP compliance and client requirements.

Responsibilities include generating validation protocols, reviewing reports, supporting investigations, and performing periodic revalidations while fostering cross-functional collaboration with Production,

Qualifications

• Bachelor's/associate degree or Diploma/Certificate in Quality/Validation required.
• Demonstrated interest in Validation and ability to follow clear goals.
• Proficient with Microsoft Office and able to support GMP/regulated activities.

Responsibilities

• Execute validation activities for Process, Facility and Equipment across PCI sites.
• Generate validation protocols for new and existing systems; review/approve reports.
• Support investigations, deviations and change controls as required.

Skills

Communication

Prioritization

Problem solving

Teamwork

Education

Bachelor's/Associate degree in Quality/Validation

Tools

Microsoft Office

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.

We are looking for a Validation Specialist (Permanent role) to join our team in Stamullen, County Meath. This is a Monday to Friday position, 100% on-site.

Summary of Role

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

Areas of validation included are

• Process Validation (PV)
• Cleaning Validation (CV)
• Computer Systems Validation (CSV)

Key Responsibilities

• Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS Department
• Ensuring all validation activities on site relating to Facility, Equipment and Processes meet the expectations of clients but more specifically meet regulatory requirements (HPRA/ FDA).
• Comply with Site Validation Master Plan.
• Generate validation protocols for new and existing computer systems, facilities, equipment and processes and review/approve all reports. Also to generate and maintain documentation for cleaning validation performed at PCI sites in Ireland.
• Execute validation activities, with minimal supervision, in conjunction with Technical, Production and Engineering functions.
• Perform sampling in support of validation studies, including AQL, and cleaning validation.
• Manage tooling validations and associated documentation.
• Ensure the strict implementation of validation procedures plus the timely and accurate completion of all validation documentation.
• Support complaint investigations, deviation investigations and change controls as required.
• To undertake such tasks and to manage specific or ad hoc projects as and when required to meet business needs and within the scope of the job-holder's capabilities.
• Identify and support opportunities for improving processes and or procedures.
• Perform Periodic reviews and revalidations on a scheduled basis.
• Work with Validation team to ensure a robust and compliant validation system is in place.
• Ensure validation being performed is in line with industry standards and latest regulatory guidelines.
• Carry out various other additional tasks that may be required from time to time in accordance with the overall goal of the company.

Essential

• Bachelor's or associate degree or Diploma / Certificate in Quality / Validation. May substitute experience in lieu of educational requirements.
• Minimum 2 years' experience working in Manufacturing or Quality.
• Demonstrate interest in Validation.
• Capability to follow clear goals, communicate clearly and ensure progress to completion meeting predefined targets.
• Ability to manage multiple tasks and set priorities.
• Problem Solving and Troubleshooting skills. The successful candidate should display a dynamic and proactive approach to manage problems.
• Self-motivated with a results driven approach.
• Flexibility to work across different shifts on request in line with business needs.
• Adaptable and ability to work collaboratively.
• Proficient in Microsoft Office products (incl. Excel, PowerPoint, Word, etc.).
• Experience in a GMP or Regulated Environment.

Desirable

• Experience in Lean Manufacturing, including experience in Lean tools to develop continuous improvements.

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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.