Validation Engineer

This Validation Engineer will be responsible for equipment/facility validation projects in a hands on role including writing validation protocols, scheduling and executing testing, gathering and analyzing data, and writing validation summary reports. This person will participate as a supporting member representing validation on project teams. Validation Engineers will lead specific validation projects. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: Design required validation studies and write protocols for the facility and equipment. Coordinate resources required to complete validation studies in a timely manner. Execute validation studies per required schedules in a safe, compliant manner (e.g. LOTO). Analyze test data and report questions/issues. Lead and document investigations of failed validation test results. Complete validation protocols and validation summary reports with necessary approvals. Support the review of new systems and modifications to existing systems to ensure designs comply with cGMPs and are able to be validated and maintained in a validated state. Maintain validation equipment and supplies to enable validation to be completed per schedule requirements. Support the development of required validation procedures and practices with respect to the facility. Identify issues and/or improvements to validation procedures, practices, and policies related to validation, equipment and processes. Basic Qualifications Bachelor's degree in a scientific discipline OR 2+ years of experience working in a regulated GMP environment with an Associated degree On site role Preferred Qualifications 1+ years of experience in Validation, Automation or Process engineering Familiar with cGMPs. Strong interpersonal and organizational skills. Technical understanding of the industry and validation practices related to the pharmaceutical industry is preferred. Strong verbal and written communication skills. Must be able to interact well with peers and senior personnel in multidisciplinary teams involving scientific, engineering, and operational disciplines. Able to take directions and effective at implementing decisions. Must have strong technical writing skills Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at View email address on click.appcast.io Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at #J-18808-Ljbffr