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YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_b42cb6a3-900"},"title":"Mitarbeiter Produktions-Compliance - MBR-Erstellung und Dokumentenmanagement","description":"<p>Are you looking for a challenging and meaningful career where you can make a real difference? We are seeking a highly motivated and experienced professional to join our team as a Production Compliance Specialist - MBR Creation and Document Management.</p>\n<p>As a Production Compliance Specialist, you will be responsible for creating and managing manufacturing instructions (MBRs) in our Manufacturing Execution System (MES), including creating MBR checklists. You will also create and review product quality reviews for the bulk production/forming area, create and manage machine recipes from production instructions, and conduct research for the forming area.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Create and manage manufacturing instructions (MBRs) in MES, including creating MBR checklists</li>\n<li>Create and review product quality reviews for the bulk production/forming area</li>\n<li>Create and manage machine recipes from production instructions</li>\n<li>Conduct research for the forming area</li>\n<li>Create, coordinate, and implement change requests in MOC for the department</li>\n<li>Participate in projects and support implementation for the forming area</li>\n<li>Support the creation of cleaning instructions (eCRs) in MES, preparation and timely provision of production orders, and creation, reconciliation, and archiving of GMP documents for the forming area (e.g., SOPs, OIs, forms, risk analyses, etc.)</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree in pharmacy or related field</li>\n<li>First-hand experience in the pharmaceutical industry, preferably in the manufacture of medicinal products and GMP documentation</li>\n<li>Good knowledge of GMP guidelines</li>\n<li>Strong quality awareness</li>\n<li>Proficiency in Microsoft Office applications (Outlook, Word, PowerPoint, Excel) and MES and document management systems</li>\n<li>High level of initiative and self-motivation</li>\n<li>Excellent communication and teamwork skills</li>\n<li>Very good German language skills and basic English language skills</li>\n</ul>\n<p>What we offer:</p>\n<ul>\n<li>Competitive salary between €3,552 and €3,765 per month (full-time) plus annual bonus, holiday pay, and Christmas bonus/13th month salary</li>\n<li>Opportunities for further development through access to learning opportunities such as LinkedIn Learning and our language learning platform Education First</li>\n<li>Support for health and a self-care lifestyle</li>\n<li>Confirmation of sustainable mobility through climate-friendly mobility options such as job ticket and leased company bike</li>\n<li>Exciting benefits and access to discounts from over 150 brands through our Corporate Benefits Program</li>\n<li>Celebration of diversity in an inclusive work environment where you are welcome, supported, and encouraged to bring your whole personality</li>\n</ul>\n<p>Further information: The position is limited to 2 years. Be You. Be Bayer#LI-AMSEMEA</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_b42cb6a3-900","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Bayer","sameAs":"https://talent.bayer.com","logo":"https://logos.yubhub.co/talent.bayer.com.png"},"x-apply-url":"https://talent.bayer.com/careers/job/562949976635767","x-work-arrangement":"onsite","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["GMP guidelines","Microsoft Office applications","MES and document management systems","Manufacturing instructions (MBRs)","Product quality reviews","Machine recipes","Research","Change requests","Cleaning instructions (eCRs)","GMP documents"],"x-skills-preferred":[],"datePosted":"2026-04-18T22:11:02.282Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Weimar"}},"employmentType":"FULL_TIME","occupationalCategory":"Manufacturing","industry":"Pharmaceuticals","skills":"GMP guidelines, Microsoft Office applications, MES and document management systems, Manufacturing instructions (MBRs), Product quality reviews, Machine recipes, Research, Change requests, Cleaning instructions (eCRs), GMP documents"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_b6b51efd-c8b"},"title":"Technical Writer","description":"<p>We are seeking a Technical Writer to join our team in Oak Ridge, TN. As a Technical Writer, you will develop, maintain, and control technical documentation across engineering, manufacturing, and quality functions. This role ensures that procedures, work instructions, and records are accurate, accessible, and compliant with company and regulatory requirements.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Develop, edit, and maintain technical documents including procedures, work instructions, specifications, and reports</li>\n<li>Translate engineering and manufacturing processes into clear, user-friendly documentation</li>\n<li>Standardize document structure, formatting, and language across departments</li>\n<li>Review and revise documentation to ensure accuracy and alignment with current processes</li>\n</ul>\n<p>Document Control &amp; Records Support:</p>\n<ul>\n<li>Support management of controlled documents through revision, approval, and release processes</li>\n<li>Maintain version control and ensure documents are current and accessible</li>\n<li>Ensure records are properly organized, stored, and retrievable in accordance with company procedures</li>\n<li>Assist with document change control and configuration management processes</li>\n</ul>\n<p>Compliance &amp; Audit Support:</p>\n<ul>\n<li>Ensure documentation aligns with applicable standards (e.g., NQA-1, ISO 9001, DOE/NRC requirements as applicable)</li>\n<li>Support internal and external audits by providing documentation and records</li>\n<li>Maintain audit-ready documentation and support document retention practices</li>\n</ul>\n<p>Cross Functional Coordination:</p>\n<ul>\n<li>Work closely with engineering, quality, and operations teams to gather technical information and validate content</li>\n<li>Support rollout and implementation of new or revised procedures and work instructions</li>\n<li>Assist teams in understanding documentation requirements and best practices</li>\n</ul>\n<p>Systems &amp; Process Improvement:</p>\n<ul>\n<li>Support implementation and improvement of document management and records systems</li>\n<li>Identify opportunities to improve documentation workflows, clarity, and usability</li>\n<li>Develop templates and guidelines for consistent technical documentation</li>\n</ul>\n<p>SKILLS &amp; QUALIFICATIONS:</p>\n<ul>\n<li>Bachelor’s degree in Technical Writing, Engineering, Science, Business, or a related field; or equivalent experience</li>\n<li>2–5 years of experience in document control, technical writing, or records management in a regulated or industrial environment</li>\n<li>Strong writing, editing, and document organization skills with high attention to detail</li>\n<li>Experience translating technical or engineering content into clear documentation</li>\n<li>Familiarity with document control or quality systems (e.g., NQA-1, ISO 9001, or similar)</li>\n<li>Experience with document management systems, ERP, or quality systems</li>\n<li>Proficiency in Microsoft Office (Word, Excel) and document formatting tools</li>\n<li>Ability to manage multiple documents and priorities in a fast-paced environment</li>\n<li>Experience in nuclear, aerospace, defense, or other regulated industries is a plus</li>\n</ul>\n<p>Benefits:</p>\n<ul>\n<li>Health, Dental &amp; Vision Insurance</li>\n<li>Health Savings Account</li>\n<li>Disability and Life Insurance</li>\n<li>401K Plan</li>\n<li>Paid Time Off, Holidays</li>\n</ul>\n<p>Work Environment:</p>\n<ul>\n<li>This role is based in Oak Ridge, TN and involves a combination of office-based work and regular interaction with engineering, manufacturing, and quality teams.</li>\n<li>The position requires detailed documentation work, coordination across departments, and participation in audits and compliance activities. Occasional time in manufacturing or laboratory environments may be required to ensure documentation accuracy. Reasonable accommodation will be provided to enable individuals with disabilities to perform the essential functions.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_b6b51efd-c8b","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Standard Nuclear","sameAs":"https://www.standardnuclear.com/","logo":"https://logos.yubhub.co/standardnuclear.com.png"},"x-apply-url":"https://job-boards.greenhouse.io/standardnuclearinc/jobs/5187586008","x-work-arrangement":"onsite","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Technical Writing","Document Control","Records Management","Quality Systems","Document Management Systems","ERP","Microsoft Office","Document Formatting Tools"],"x-skills-preferred":[],"datePosted":"2026-04-17T13:01:57.880Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Oak Ridge, TN"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Manufacturing","skills":"Technical Writing, Document Control, Records Management, Quality Systems, Document Management Systems, ERP, Microsoft Office, Document Formatting Tools"}]}