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Supplier Quality Specialist (2813145273)

Technology 信息技術

IT Auditor


GCSE/Scottish Standard Grades A-Level Postgraduate or above 碩士或以上 Undergraduate or above 學士或以上 Intermediate apprenticeship 學徒

PSW Apprenticeship 學徒 華語工作 Contract 合同制 Full-Time 全職 Internship 實習 Part-Time 兼職


Reading, Berkshire, United Kingdom

At ConvaTec, our vision is to develop pioneering trusted medical solutions to improve the lives we touch. We are a global medical technology business focused on serving people and care givers in the areas of advanced wound care, ostomy care, continence and critical care and infusion care. We devise, develop, and manufacture innovative products and services that support people with deeply personal and challenging medical conditions, helping to improve care for them and giving them greater confidence, freedom and mobility. We are guided by our five core values, that shape the way we work, every day: Improve Care, Deliver Results, Grow Together, Own It and Do What’s Right. We are a global Group, with over 9,900 employees and in 2020, our Group generated revenues of over $1.894 billion. To learn more about ConvaTec, please visit At ConvaTec we’re transforming our business for the better. Better products. Better ways of working. And better ways of delivering for our customers and each other. We’re aiming for nothing short of excellence. Join us as a Supplier Quality Specialist and you’ll do the same. Job Summary Responsible for the quality assurance activities for the External Manufacturing business and its suppliers, including change control, lot release, product documentation updates, and other supplier management activities. Represent quality department in final release for product batches to support base business and to ensure compliance to specifications and documentation requirements. Execute supplier quality responsibilities such as change control initiation and execution, maintain batch certificates, write rework protocols, escalate nonconforming materials, and communicate directly with suppliers. Support various global supplier quality initiatives involving supplier audits, scheduling, new product launches, and quality/technical documentation. Responsible for process and supplier metrics. Responsible for assisting the External Manufacturing team as needed to ensure timely product release and compliance to internal operating procedures. Duties And Responsibilities This role will primarily be responsible for the following activities within the Global Supplier Quality team: Support third party product release process for all Global suppliers Develop and maintain training materials, standard operating procedures, and work instructions to support the External Manufacturing Quality process. Maintain a strong relationship with all Global suppliers to ensure Quality Control and Compliance for daily operations along with New Product Introductions and Base Business Changes. Plan and conduct meetings and presentations related to supplier issue and/or base business project in Supplier Quality. Maintain strong understanding of quality documentation to provide guidance and solutions for internal and external contacts. Manage and communicate with suppliers to correct any errors in the product documentation Work with corporate team and suppliers to author rework protocols Initiate and execute Change Control with supplier and develop the document management plan for External Manufacturing and update it, as needed. Maintain Monthly Key Performance Indicator (KPI) metrics utilizing strong data mining skills for the External Manufacturing business. Manage organizational documentation through the document life cycle. Ensure that organizational documents go through a documented and approved review-and-approval process before being stored. Provide support during corporate inspections. Execute or support global supplier management activities such as audits, scheduling, or performance ratings Principal Contacts Internal: Directors, Managers, Engineers, & Supervisors (all departments) External: Global Third Parties Suppliers Travel Requirements: Yes - International travel (10%) Language Skills Required Speaking: Yes English Writing/Reading: Yes English Required Education/Qualifications: Bachelor’s degree in relevant field, required. Preferred Training Requirements Introduction training for administrative employees Quality System documents and procedures relevant to all employees (local and ConvaTec corporate e.g. Code of Conduct& Ethics, Quality Policy, Complaints reporting, Good manufacturing practice ) , including regular re-training when required Quality System documents and procedures relevant to training and education of personnel (local) Quality System documents and procedures relevant to job performance Required Experience: One (1) to two (2) years of experience in the area of quality document management / document control is preferred. Experience with External Manufacturing with regards to Doc Control and Quality preferred but not required. Advanced SQL database skills. Advanced Data mining skills. Detailed analytical abilities. Strong experience project management. Strong prioritization and coordination skills. Ability to work with electronic databases (i.e. Documentum). Effective communication with key customers within a diverse organization (Operations, R&D, Quality, Supply Chain, Regulatory Affairs, Clinical Affairs, Marketing, Information Management). Advanced computer management skills including Microsoft Word, Excel and Visio. Proactive and flexible to meet priorities and achieve deliverables. Knowledge of the principles of document control, supply chain systems, change control, Quality Systems and Quality Systems of Medical Devices. Required Competencies: Good communication level, Ability to develop partnership internally and externally Managerial, leadership skills Working Conditions Work in the office on PC or remote Our ambitions will bring the very best out in you. You’ll be pushed to aim higher and really own your work. You’ll be encouraged and supported to make things happen, too. It can be challenging. But, as the progress you make will help improve the lives of millions, it’ll be worth it.This is stepping up to a challenge. This is work that’ll move you. Beware of scams online or from individuals claiming to represent ConvaTec A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official ConvaTec email address. If you receive a suspicious approach over social media, text message, email or phone call about recruitment at ConvaTec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at . Equal opportunities ConvaTec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law. Notice to Agency and Search Firm Representatives ConvaTec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any ConvaTec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of ConvaTec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Already a ConvaTec employee? If you are an active employee at ConvaTec, please do not apply here. Go to the Career Worklet on your Workday home page and View "ConvaTec Internal Career Site - Find Jobs". Thank you