Validation Engineer (Manufacturing)
Global Medical Device Manufacturing Company
Leesburg, VA
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Job DescriptionThis position is a quality testing engineer in manufacturing company and not I.T Testing. We are looking for someone who has experience working in manufacturing or medical device company doing validation testing and engineering. Job Description:Implementing the company's validation strategy, based on Corporate procedures and regulatory requirements.Supporting validation activities by providing guidance and expertise to authors of validation documentation and executors of validation protocols at the local site.Reviewing and approving of validation documentation to ensure compliance with regulations and validation best practices.Will work within the QA Shared Services Validation Team, responsible for validation related activities, including, but not limited to the following:Having knowledge of and ability to provide Interpretation and Guidance on Regulations, Corporate, Divisional and Site Local procedures as they relate to validation activities.Participating within Corporate Validation Team to develop and revise Validation Procedures and Templates to ensure that Current Regulatory Compliance and Company Objectives are maintained.Participating on both Corporate and Local Validation Teams to discuss / give feedback and approve revisions to Validation Procedures.Representing validation at both internal and external audits.Ensuring that Validation Practitioners receive training/coaching to allow them to effectively support and/or perform validations for current and anticipated projects.Ensuring that appropriate Systems are in place to evaluate changes to Validated/Qualified Systems to ensure their continued validated/qualified state.Ensuring that appropriate Site Validation Listing is established and controlled as per Current Regulatory and Company Requirements.Reviewing and approving of Validation/Qualification Documentation.Working with Validation Consultants/Contractors as required ensuring that Validations are completed as per corporate and divisional procedures.Being the site responsible for at least 1 validation specialty and be the primary support for that specialty and site.North America Qualification:Bachelor of Science, Engineering or related subject with 3 to 5 years of experience in validation, orMasters of Science, Engineering or related subject with 0 to 2 years of experience in validationExcellent communication skills and attention to detail.Have a good understanding of engineering and machine tool fundamentals.High level of PC skills.Must be proficient with Microsoft Word, Microsoft Excel and PowerPoint packages.Self-starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks in a fast paced environment.Must be willing to work as part of a multi-site team, be able to travel as part of the jobKnowledge of Computer System Validation including GAMP 5 and 21 CFR part 11 requirements desirable.Working knowledge/experience of Risk Based Techniques i.e. FMEAs, FTAs etc.Have a good understanding of statistical techniques, in particular statistical sampling plans, Process Capability, Gauge R&Rs.Strong knowledge of Quality Concepts (e.g. CAPA, Audits, Statistics).Highly developed problem solving and strong analytical skills.Lean Six Sigma training a distinct advantage.Company DescriptionCompany is one of the world’s leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. Offering a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neuro-technology & spine products to help people lead more active and more satisfying lives
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Posted:
Nov 17th
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