{"id":4300479,"url":"https://alion.io/job/teleflex-document-control-and-records-specialist","title":"Document Control and Records Specialist","company":{"id":1764434,"name":"Teleflex","domain":"teleflex.com","url":"https://alion.io/company/teleflex","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"SuccessFactors","truth_index":{"grade":"A","score":92,"open_postings":3,"ghost_share":0,"stale_share":0.333,"repost_share":0,"time_to_fill_p50_days":28,"computed_at":"2026-11-12T10:38:37Z"}},"role":"Administrative","role_family":"Administrative","seniority":"junior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Chelmsford, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":46700,"max":65400,"currency":"USD","period":"year","gross":null,"usd_annual":65400},"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"21 CFR Part 820","optional":false},{"name":"Agile","optional":false},{"name":"ISO 13485","optional":false},{"name":"Microsoft Office","optional":false},{"name":"Outlook","optional":false},{"name":"Veeva","optional":false}],"status":"live","first_seen_at":"2026-11-14T02:56:18Z","employer_posted_date":"2026-11-13","last_verified_at":"2026-11-14T02:56:18Z","board_verified":true,"closed_at":null,"days_open":0,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":0},"description":"Expected Travel: Up to 10%\nRequisition ID: 14732\nAbout Teleflex Incorporated\nAs a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.\nTeleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ - trusted brands united by a common sense of purpose.\nAt Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.\nGlobal Operations - Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.\nPosition Summary\nThe Document Control & Records Specialist supports the Quality Systems function by administering document control, records management, and change control activities within the Quality Management\nSystem (QMS). This position ensures the integrity, accuracy, accessibility, and compliance of controlled documents and records while supporting cross-functional teams in the timely execution of change management processes and regulatory requirements.\nPrincipal Responsibilities\nAdminister document control activities within the Quality Management System (QMS), including document creation, review, approval, issuance, revision, archival, retention, and obsolescence.\nProcess and track document change requests, engineering change orders (ECOs), and other controlled quality system records through completion.\nExecute document and change management processes within Agile, Legacy Agile, and other applicable systems.\nMaintain controlled documentation and records in accordance with FDA regulations, ISO 13485 requirements, company policies, and Good Documentation Practices (GDP).\nEnsure the accuracy, integrity, organization, and accessibility of quality records and documentation.\nPerform accurate data entry and maintenance of document control databases and record repositories.\nCoordinate document distribution activities and ensure timely communication of document releases, revisions, and obsolescence notifications.\nCollaborate with cross-functional teams to support the timely review, approval, and implementation of document and process changes.\nSupport internal, customer, and regulatory audits by providing documentation and records as requested.\nAssist with records retention and archival activities in accordance with company procedures and regulatory requirements.\nProvide backup support for training administration activities, including training record maintenance and documentation.\nMaintain effective working relationships and communicate professionally with employees at all levels of the organization.\nComply with all applicable FDA regulations, quality system requirements, company policies, operating procedures, and safety requirements.\nPerform other duties and responsibilities as assigned.\nEducation / Experience Requirements\nMinimum of 2 years of experience in document control, records management, quality systems administration, training administration, or a similar regulated environment.\nExperience working within FDA-regulated, medical device, pharmaceutical, biotechnology, or other highly regulated industries preferred.\nProficiency with Microsoft Office applications, including Word, Excel, PowerPoint, and Outlook.\nDemonstrated attention to detail, accuracy, and organizational skills.\nSpecialized Skills / Other Requirements\nWorking knowledge of document control and records management principles.\nExperience with electronic document management systems (eDMS) and quality systems software preferred.\nWorking knowledge of Agile PLM, SAP, and Veeva Vault strongly preferred.\nFamiliarity with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, and Good Documentation Practices (GDP) preferred.\nStrong verbal, written, and interpersonal communication skills.\nAbility to prioritize multiple tasks and manage competing deadlines in a fast-paced environment.\nStrong problem-solving and organizational skills with exceptional attention to detail.\nAbility to work independently while effectively collaborating within a team environment.\nDemonstrated proficiency in maintaining confidentiality and handling controlled information.\nWorking Conditions / Physical Demands\nThe pay range for this position at commencement of employment is expected to be between ($46,700-$65,400) however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position will also include benefits such as medical, prescription drug, dental and vision insurance, flexible spending accounts, participation in 401(k) savings plan, and various paid time off benefits, such as PTO, short- and long-term disability and parental leave, dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.\nAt Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.\nTeleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or .\nTeleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.\n© 2026 Teleflex Incorporated. 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