Job Description
Senior R&D Quality Officer (12 month fixed contract) Date: Oct 2, 2024 Location: Waterford, Ireland, X91 Job Id: 58431 We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point.We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world. We would like to invite applications for the role of Senior R&D Quality Officer at our site in Waterford. The role of the Senior R&D Quality Officer involves overseeing the quality processes required to support on-site research and development activities. The position offers a diverse range of responsibilities and ample opportunities for advancement for the successful candidate.A Day in the Life of our Senior R&D Quality Officer...Support new product introduction and new equipment/system introduction and ensure system, process, and all operations is in line with regulations and industry best practice, within required timelines. Ensure timely documentation review and product release is in line with regulatory requirements and to the required customer service levels.Ensure all clinical customer complaints are logged, investigated and closed out in a timely manner all in accordance with cGMP’s and company procedures, in order to meet the objectives of the Quality Function.Ensure software validation is carried out in compliance with site/corporate policies and SOP’s.Ensure R&D projects are in compliance with regulatory requirements and adhere to current US/EU guidelines.Provide the R&D department with Quality Assurance support for all clinical/submission batches, quality systems, IVBE studies, Device Design, Combination Products and support for all new product development project teams.Provide the R&D department with guidance regarding clinical trial manufacture and new product development and introduction.Who we are looking forEducated to Degree level in Pharmaceutical/Life Sciences.Experienced in a Pharmaceutical, Medical Device or QA environment.Experienced in Regulatory/Notified Body inspections.Do you have…In depth knowledge and understanding for interpretation of cGMPs and Regulatory requirements for Combination Products / Medical Devices / IMPs.Experience with report writing, Project Management, Continuous Improvement and problem solving tools.Understanding of production and laboratory systems to effect judgement decisions consistent with quality and business needs.Knowledge and understanding of software validation / medical device requirements is desirable.Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. #J-18808-Ljbffr