Role Description - Leads activities to define document product requirements - Develops and executes plans to ensure products meet technical, data, and regulatory requirements - Leads configuration control of documents and artifacts - Tracks release quality metrics - Leads projects, managing schedule, cost, and performance Qualifications - Bachelor's Degree - Excellent communications skills, ability to interact with senior internal and external personnel on significant matters and cross-team coordination - Understanding of configuration management (CM) and document CM, including processes and tools Requirements - Experience with BEDS - Experience with web-based services and tools - Experience with software release processes Benefits - Competitive base pay and variable compensation opportunities - Health insurance - Flexible spending accounts - Health savings accounts - Retirement savings plans - Life and disability insurance programs - Programs that provide for both paid and unpaid time away from work

Role Description Under general supervision, the Clinical Product Surveillance Specialist is responsible for independently using knowledge of clinical workflows and product use when investigating post-market complaints and providing clinical resource support to internal and external customers. This role acts as a patient safety advocate and participates in various cross-functional activities that include, but are not limited to Complaint Handling, Risk Management, Design Quality, and Regulatory Compliance, to support product safety and efficacy and recommend improvements and/or corrections as needed. Responsibilities - Identify and investigate domestic and international post-market complaints with a potential safety issue and escalate complaints for further investigations as needed. - Ensure adverse event reports (i.e. MDRs, ICSRs) are processed, prepared, and submitted to the FDA within regulation timelines. - Process FDA reportable post-market complaints and assist in coordinating international adverse event reporting with local health authorities or authorized representatives. - Collaborate with team members and act as a clinical resource for internal and external customers. - Ensure communications are created and issued to internal and external customers. Review customer responses for technical and clinical accuracy as related to Medline products. - Provide clinical insight, evaluation, and resolution during post-market, risk management, and design development/modifications processes for new and existing Medline products. - Participate in the analysis of safety and risk data within areas of responsibility and identify actionable findings, trends, or product safety issues that require further investigations. - Assess clinical, health, and safety risks during Health Hazard Evaluations, product recall or field action determinations, and acceptance of product as-is. - Ensure compliance with applicable post-market regulations for areas of responsibility and participate in regulatory audits, regulatory body communications, and/or additional information requests as applicable. - Participate in process improvements and Corrective and Preventative Actions (CAPAs). - Participate in the development and maintenance of processes/procedures associated with Adverse Event Reporting, Risk Management, and Standard Operating Procedures (SOPs) associated with Clinical Risk Evaluation. - Facilitate clinical safety meetings and conduct trainings related to post-market surveillance, clinical use, product risk, and SOP requirements. - Maintain active Registered Nurse (RN) licensure and good standing with state or other governing licensure body. Qualifications - Bachelor's Degree in Nursing (BSN) with at least 5 years of patient care experience OR a BSN with 4 years or less of patient care experience and 2 years of experience in a similar role. - Actively licensed as an RN to administer healthcare and in good standing with state or other governing licensure body. - Knowledge of quality improvement and patient safety. - Understanding of clinical standards, processes, and workflows. - Familiarity with medical devices and pharmaceuticals related to patient safety. - Ability to assess clinical outcomes, analyze data, and present findings to various audiences. - Proficiency in Microsoft Office (Outlook, Teams, Excel, Word, PowerPoint). - Strong work ethic and proactive approach to responsibilities. - Customer-focused with a results-oriented mindset. - Ability to make sound judgments prioritizing patient safety. - Team player with analytical skills and a positive attitude. - Experience in data analysis and reporting to identify trends and solutions. - Experience working with cross-functional teams to solve complex problems. - Effective time management skills to handle multiple projects and deadlines. - Ability to work independently and escalate issues when necessary. - Problem-solving skills to overcome obstacles and find successful solutions. Preferred Qualifications - Advanced degree in nursing, medical or healthcare sciences, or other healthcare related field. - Licensed, registered, or certified by a state or other governing body to administer health care. Certification in a nursing specialty (i.e. APRN, CNS, CEN, CCRN, WOCN, etc.) or other healthcare related field. Work Experience - Experience within a Perioperative/OR, Critical Care (i.e. Emergency Department, ICU, Step-Down ICU, Cath Lab, etc.), or Wound Care/Management setting. - Experience in clinical, medical device, or pharmaceutical risk management and/or within the medical device or pharmaceutical industry. - Experience or working knowledge of government and industry standards and regulations for medical products (i.e. 21 CFR 803, 21 CFR 314, 21 USC 379aa, 21 CFR 7, ISO 13485, ISO 14971, etc.). Benefits - Health insurance - Life and disability insurance - 401(k) contributions - Paid time off Salary Information The anticipated salary range for this position: $79,000.00 - $119,000.00 Annual. The actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold. Company Description Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization. We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

Role Description Olen Kari Äikäs, Head of Facilities, ja etsin henkilöä, joka on valmis kasvamaan kanssamme. Olemme kannustava ja tulevaisuuteen katsova tiimi, joka keskittyy Telian laitetilojen teknisiin ratkaisuihin ja niiden toimintavarmuuden kehittämiseen. - Vastaat Telian laitetilojen jäähdytys- ja ilmanvaihtojärjestelmien kokonaisuudesta sekä niiden kehittämisestä. - Kehität laitetilojen HVAC-ratkaisuja ja hallitset niiden elinkaarta. - Luot suunnitelmia ja ratkaisuja investointitarpeisiin ja kustannustehokkuuteen. - Konsultoit sidosryhmiä ja toimit yhteistyössä urakoitsijoiden kanssa. - Varmistat kriittisten tilojen korkean käytettävyyden ja toimintavarmuuden. Qualifications - Kyky yhdistää tekninen osaaminen, kokonaisuuksien hallinta ja yhteistyö eri sidosryhmien kanssa. - Vahva kokemus HVAC- tai LVI-ratkaisuista. - Hyvä tuntemus jäähdytys- ja ilmanvaihtojärjestelmistä. - Kyky hallita laajoja kokonaisuuksia ja edistää projekteja. - Sujuva suomen ja englannin kielen taito. Benefits - Avaimet onnistumiseen ja mahdollisuus kasvuun. - Hyvät henkilöstöedut ja työvälineet. - Mahdollisuus etätyöhön, myös ulkomailla. - Tilaisuus oppia ja kehittyä kriittisten laitetilojen HVAC-ratkaisujen ja elinkaaren hallinnan parissa. - Mahdollisuus vaikuttaa televerkon infrastruktuurin kehittämiseen ja toimintavarmuuteen. - Erinomainen esihenkilötyö, kannustava ilmapiiri ja oppimismahdollisuudet. Application Information Odotamme innolla hakemustasi viimeistään 28.6.2026. Prosessin aikana suoritetaan tarvittavat turvallisuusselvitykset. Haluatko tietää lisää tästä roolista? Ota yhteyttä: Kari Äikäs, Head of Facilities – kari.aikas@teliacompany.com Diversity and Inclusion Telialla tunnistamme osaamisen ammatillisten taitojen ja kasvupotentiaalin kautta. Edistämme monimuotoisuutta ja huolehdimme siitä, että jokaisen yksilölliset tarpeet huomioidaan – riippumatta vammaisuudesta, sukupuolesta, iästä, kansallisuudesta, seksuaalisesta suuntautumisesta tai sosiaalisesta taustasta. Yhdessä olemme sitoutuneet rakentamaan osallistavan työympäristön, jossa sinun ainutlaatuisuutesi on meidän vahvuutemme.

Role Description - Handles complex regulatory functions. - Work closely with other internal staff, departments, executive level management, customers, and government agencies to deliver a high level of service to customers. - Provide impeccable customer service. - Act as subject matter experts to provide guidance, education, and answer questions to internal and external customers. - Solicit and maintain all customs compliance documentation with customers. - Must be able to handle confidential or sensitive information and projects. - Ensure all government and organizational policies are followed. - Participate in customer, departmental, and company meetings. - Train team members as needed. - Confirm receipt of government inquiries and ensure matters are resolved timely. - Handles miscellaneous clerical functions for the Regulatory department. - Handles complex regulatory functions that include but are not limited to CF28s, CF29s, seizure notices, redelivery notices, FDA registrations, etc. - Review quality referral disputes for accuracy as an impartial mediator. - Monitor and update miscellaneous Regulatory owned reporting. - Brokerage system maintenance resulting from government updates. - Review company procedures for accuracy and ensure compliance. - Performs other duties as assigned. Qualifications - Bachelor's degree or equivalent experience, preferably in a business field. - Three (3) years industry experience required. - Regulatory experience preferred. - CCS and/or Brokers license preferred. - QDM Apprentice required. - A thorough knowledge of customs regulations, harmonized tariff schedule, and any other federal agency laws, regulations, procedures governing the customs brokerage industry with preferred emphasis in post-entry processes. - Demonstrated organizational skills to prioritize and manage multiple work assignments in a time-sensitive atmosphere. - Excellent communication skills, verbal and written. - Organizational and problem-solving skills. - Detail-oriented. - Ability to handle high volume and time-sensitive work. - Ability to work independently with minimum supervision. Requirements - Pay Transparency: This compensation range is provided as a reasonable estimate of the current starting salary range for this role across all potential locations. - Actual starting pay would be determined by experience relative to the job, market level, pay at the location for this job, and other job-related factors permitted by law. - An employee may be eligible for additional pay, premiums, or bonus potential. Benefits - Health, vision, and dental insurance. - Retirement. - Tuition reimbursement. Company Description FedEx Logistics provides freight forwarding, as well as import and export services that allow companies to reach markets throughout the world. They help customers of all sizes solve the intricacies of shipping goods globally by providing comprehensive international ocean and air freight forwarding, surface transportation and distribution, customs brokerage, trade and customs advisory services, and advanced e-commerce and trade facilitation solutions. FedEx Logistics is an Equal Opportunity Employer including, Vets/Disability.