About this opportunity
Formulated Solutions lists this IT Validation Engineer opportunity in largo, Florida. Review the employer’s description below for duties, qualifications and application requirements.
Job description
THE COMPANY:
Formulated Solutions is redefining the Pharmaceutical and Self-Directed Consumer Healthcare CDMO experience through creativity and invention; delivering our world class Marketing Partners unmatched formulations, innovative packaging and cost effective, reliable supply.
Formulated Solutions is and shall always be a company of people with the knowledge and dedication to provide our Marketing Partners with a single source solution for delivering quality and innovative products to market. We shall embrace changes and new opportunities as a vehicle to continually develop and grow sustainable relationships. As a company we shall never accept anything less than a culture that fosters creativity, growth, and profitability for both our Partners and the company.
PRIMARY PURPOSE:
Formulated Solutions is seeking an IT Validation Engineer to own system validation activities across the company. This role's initial and primary focus will be the validation of the eBR (electronic Batch Record) system as FS transitions manufacturing lines from paper batch records to eBR. The Validation Engineer will build and maintain the User Requirements Specification / Requirements Traceability Matrix (URS/RTM), coordinate the documentation and sign-off process across internal stakeholders and customers, and ensure that all validation work is complete, defensible, and audit-ready. This role will also lead the transition of FS's validation program off of Excel-based tracking and onto a dedicated validation management tool. As FS's validation program matures, this role will expand to cover validation of other systems and equipment across FS sites.
MAJOR DUTIES AND RESPONSIBILITIES:
eBR Validation & URS/RTM Ownership
Own and maintain the URS/RTM (User Requirements Specification / Requirements Traceability Matrix) Excel workbook for eBR validation projects.
Review existing paper batch records and work with Operations and Quality to capture and document the underlying requirements in the URS/RTM.
Trace each captured requirement through to its corresponding test case and result, maintaining the RTM as the source of truth for requirement coverage.
Keep the URS/RTM current as requirements change, and use it as the traceability backbone for validation testing and sign-off.
Lead the evaluation and adoption of a dedicated validation management tool, driving FS's transition away from Excel-based URS/RTM tracking toward a purpose-built system.
Validation Documentation & Sign-Off
Oversee preparation of Management of Change (MOC) documentation and shepherd each MOC through internal and customer approval.
Own the Configuration Specification documentation for validated systems, ensuring it accurately reflects the as-built configuration.
Author and manage the Validation Summary Report for each validation effort, consolidating testing results and open items.
Draft User Acceptance Test (UAT) scripts, dry-run them internally ahead of formal execution, and lead execution of UATs with internal stakeholders and customers.
Track outstanding sign-offs across all validation documents and proactively follow up with internal approvers to keep projects moving.
Customer Coordination
Serve as a primary point of contact with customers (e.g., Bayer) on validation documentation and approvals.
Package and submit validation documentation to customers in the format and process they require, and follow up to obtain timely customer sign-off.
Communicate validation status, risks, and timelines clearly to both internal leadership and customer counterparts.
Broader System Validation
Serve as the company-wide owner for system validation, extending validation practices beyond eBR to other systems and equipment as priorities dictate.
Perform risk assessments and validation testing for system upgrades and patches to validated systems, ensuring continued compliance and audit-readiness.
Conduct internal periodic reviews of validated systems to confirm they remain in a validated state and to identify any drift requiring remediation.
Help establish and continuously improve FS's validation processes, templates, and standard practices.
Support internal and customer audits by ensuring validation documentation is organized, complete, and readily accessible.
QUALIFICATION:
Required:
Bachelor's degree in Engineering, Life Sciences, Computer Science, or a related technical field, or equivalent hands-on validation experience.
3+ years of experience in validation or quality systems within a regulated manufacturing environment (pharmaceutical, consumer health, medical device, or similar GxP setting).
Working knowledge of computer system validation (CSV) / Computer Software Assurance (CSA) concepts and documentation — URS, risk assessment, Configuration Specification, IQ/OQ/PQ, and Validation Summary Reports.
Familiarity with data integrity principles (ALCOA+) and applicable regulations such as FDA 21 CFR Part 11 and cGMP.
Strong Excel skills, with experience building and maintaining detailed tracking workbooks such as a URS/RTM.
Preferred:
Direct experience validating an electronic batch record (eBR) or MES platform (e.g., Tempo/Werum PAS-X or similar) in a manufacturing environment.
Experience working directly with customers or external auditors on validation deliverables and sign-off.
Familiarity with Management of Change (MOC) / change control processes in a GxP environment.
Experience in contract manufacturing or a multi-site manufacturing organization.
Experience selecting, implementing, or administering a dedicated validation management or quality management software tool.
Excellent written communication and documentation skills; comfortable authoring formal validation deliverables.
Strong organizational skills and the ability to manage multiple documents, approvals, and stakeholders concurrently.
This role is based on-site at FS's Largo, FL facility, with approximately 5% travel to the Cleveland, TN manufacturing site. Work is performed in both office and manufacturing/production environments; time on the production floor should be expected when capturing requirements or supporting concurrent runs.
⚠️ Recruitment Disclaimer
We kindly request that third-party recruiters and agencies do not contact us regarding any job postings . All hiring is managed internally, and unsolicited outreach or candidate submissions will not be considered.
Worksite address
largo, FL, 34640, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.