Overview
Validation Specialist (Wilson, NC, US, 27893)
We are Reckitt
​Research & Development​
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
About the role
The QA Validation Specialist is responsible for executing and supporting validation activities across computerized systems, manufacturing processes, and equipment. This role ensures compliance with regulatory requirements and internal quality standards, contributing to the integrity and reliability of GxP operations.
Your responsibilities
- Support validation of GxP-regulated systems (LIMS, MES, ERP) and equipment (manufacturing, lab, utility).
- Execute IQ/OQ/PQ and process validation for new products, scale-up, and tech transfers per site master plan.
- Maintain SDLC and validation documentation (URS, risk assessments, traceability, reports) in line with Reckitt and regulatory standards.
- Ensure compliance with 21 CFR Part 11, Annex 11, GAMP 5, and data integrity principles.
- Conduct risk assessments, change control evaluations, and periodic reviews/revalidations.
- Partner with IT, system owners, Technical, and Manufacturing teams to assess risks and define validation strategies.
- Review and approve lifecycle documentation (calibration, maintenance).
- Investigate and resolve deviations, non-conformances, and support CAPAs and audit responses.
- Provide Quality support for computer system investigations.
- Participate in audits and inspections; drive continuous improvement in site operations and tech transfer practices.
- Deliver system training to ensure user competency and compliance.
- Promote best practices for electronic systems and records to maintain compliance and enhance effectiveness.
This role is not currently sponsoring visas or considering international movement at this time.
The experience we're looking for
- Minimum BS Degree in Science or EngineeringÂ
- 3+ years of experience in validation within the pharmaceutical or biotech industry.
- Strong knowledge of cGMP, FDA, EMA, ICH guidelines, and industry best practices.
- Experience with validation of automated systems, laboratory instruments, and manufacturing equipment.
- Experience with electronic validation software and enterprise systems (e.g., VeevaVault, Kneat Validation, SAP) and the ability to train end users.
- Experience in validated computer systems and knowledge of CSA / Data Integrity requirements.Â
- Experience with validation of automated systems, laboratory instruments, and manufacturing equipment.
- Experience with electronic validation software and enterprise systems (e.g., VeevaVault, Kneat Validation, SAP) and the ability to train end users.
- Experience in validated computer systems and knowledge of CSA / Data Integrity requirements.Â
- Excellent documentation, communication, and project management skills.
- Strong written/verbal communication and presentation skills. Â
- Ability to work independently and in cross-functional teams.
- Able to manage and prioritize a busy workload to achieve deadlines and meet audit requirements.Â
The skills for success
What we offer
Salary Range
USDÂ $67,000.00 – Â $101,000.00
Hiring Range:Â 67,000 – 84,000
Pay Transparency
Equality
IMPORTANT: Before applying for this role, please make sure you have the right to work in the country where the role is based. Unless it clearly stipulates within in the job advert above that the hiring company is looking to or able to sponsor applicants it is deemed that the hiring employer will only consider applications from those able to comply with and work in the country where the role is based.