mputer System Validation in Oradea

Req ID: 112982 Remote Position: NoRegion: Europe Country: Romania State/Province: Oradea City: Oradea Detailed Description: Incumbents apply in-depth knowledge in a FDA area of specialization. Work is performed within established professional standards and practices. Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors and a considerable degree of judgement. Erroneous decisions or failure to achieve results may have a negative impact on the division’s/department’s operations, schedules, and/or performance goals. Works under minimum Supervision. Seeks approval from others on matters outside of job/role scope. Receives instruction on specific assignment objectives and possible solutions. Unusual problems are solved jointly with manager. Builds internal and external relationships, with emphasis on those that facilitate the achievement of job/role accountabilities, such as relationships with key suppliers, customers and internal service. Performs tasks such as, but not limited to, the following: Gathers Business Requirements and prepares FDA compliant documents based on those requirements. Interacts with the business community and customers to understand business processes and define tools can be leveraged to optimize the business process. Ensures team members are provided with timely and accurate project information and status updates. Ensure all systems are running in compliance with company and site policies Plan, Analyse and document tests for Manufacturing Execution Systems and other site systems in compliance with FDA regulations Lead application validation Manage adjustments or improvements to equipment and processes. Lead risk analysis to identify system and process controls. Assessment of changes and impact on validated systems Ability to lead implementations of EMS related software/modules Knowledge/Skills/Competencies: Ability to Identify, gather, analyse and properly document system requirements. Capable of ensuring that documents plus practices attain quality standards and applicable regulatory conformance. Capable of performing risk analysis using tools such as FMEA Capable of implementing software validation engineering test plans, test cases/scripts. Ability to propose solutions and collaborate in software validation procedures and processes. Proven skills on implementation of computerized system validation projects with 3 years in developing computerized system validation plan and protocols. Strong written and verbal communication skills with the ability to work through technical issues with customers both remotely and in person Ability to analyze and understand business requirements and to design solution specifications This position requires a high energy level and a passion for excellence. Very good command of written & spoken English. Proven skills in projects management Organization and time management with little overall supervision. Excellent technical knowledge in specialized domains. Physical Demands: Duties of this position are performed in a normal office environment. Duties may require extended periods of sitting and sustained visual concentration on a computer monitor or on numbers and other detailed data. Repetitive manual movements (e.g., data entry, using a computer mouse, using a calculator, etc.) are frequently required. Occasional overnight travel is required. Typical Experience: 3 - 5 years of IT computer validation with experience in medical device manufacturing operation experience in a regulated environment with in depth knowledge and experience with cGMPs/GLPs/GAMP regulations related to medical device manufacturing systems, CFR Part 820, 210, 211, 21 CFR Part 11, ISO 13485, ISO 14971. ISO27001 knowledge is an advantage Typical Education: Bachelor degree in computer software, industrial, mechanical engineering or electrical engineering. Training in validation methodologies, technologies and process control computer systems. Notes: This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time.Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law). At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them. COMPANY OVERVIEW: Celestica (NYSE, TSX: CLS) enables the world’s best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud. Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers. Celestica would like to thank all applicants, however, only qualified applicants will be contacted. Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services.