{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/city/pennsylvania-marietta/"},"x-facet":{"type":"city","slug":"pennsylvania-marietta","display":"Pennsylvania - Marietta","count":6},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d2342a56-881"},"title":"Operational Quality Oversight","description":"<p>You will provide operational quality oversight at a United States manufacturing site. You will work closely with production, laboratories, engineering and quality teams to keep processes compliant, safe, and reliable.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Ensure GMP processes and personnel adhere to current GMP and regulatory requirements</li>\n<li>Maintain shopfloor oversight and be the first line of contact for quality issues</li>\n<li>Provide guidance during GMP activities to detect potential quality issues</li>\n<li>Perform spot-checks of activities across production and laboratory areas</li>\n<li>Review and approve batch records and documentation</li>\n<li>Provide review and approval of deviations and CAPA plans</li>\n<li>Ensure all GMPs, validation, quality, safety and environmental regulations are met</li>\n<li>Coach employees on the importance of following procedures</li>\n<li>Provide on-the-floor quality oversight and detect early quality risks</li>\n<li>Make or recommend disposition decisions and support lot release activities</li>\n</ul>\n<p>Basic Qualifications:</p>\n<ul>\n<li>Bachelor’s degree in biology, chemical engineering, life sciences field or equivalent</li>\n<li>2+ years of experience in regulated industry with strong quality assurance background</li>\n<li>1+ years of experience with GMP’s, NIH Guidelines, FDA and other regulatory agency compliance requirements</li>\n<li>Experience with validation principles, aseptic processing, quality systems and FDA regulations</li>\n</ul>\n<p>Preferred Qualifications:</p>\n<ul>\n<li>Experience in biologics or pharmaceutical manufacturing environments</li>\n<li>Training or experience in root cause analysis methods such as DMAIC</li>\n<li>Familiarity with inspection readiness and regulatory agency expectations</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Marietta/Operational-Quality-Specialist_446693","directApply":true,"hiringOrganization":{"@type":"Organization","name":"GSK","sameAs":"https://www.gsk.com","logo":"https://logos.yubhub.co/gsk.com.png"},"x-apply-url":"https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Marietta/Operational-Quality-Specialist_446693","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["GxP Regulations","Pharmaceutical Regulatory Compliance","Quality Assurance (QA)","Risk Awareness","Technical Writing","Data Integrity","Detail-Oriented","Digital Fluency","Influencing Without Authority","Lean Management","Problem Solving"],"x-skills-preferred":["Biologics Manufacturing","Root Cause Analysis","Inspection Readiness","Regulatory Agency Expectations","DMAIC"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-29T06:14:23.592Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Pennsylvania - Marietta"}},"employmentType":"FULL_TIME","occupationalCategory":"Operations","industry":"Healthcare","skills":"GxP Regulations, Pharmaceutical Regulatory Compliance, Quality Assurance (QA), Risk Awareness, Technical Writing, Data Integrity, Detail-Oriented, Digital Fluency, Influencing Without Authority, Lean Management, Problem Solving, Biologics Manufacturing, Root Cause Analysis, Inspection Readiness, Regulatory Agency Expectations, DMAIC"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_a99e8b31-ebd"},"title":"Plant Utilities Technician","description":"<p>The Plant Utilities Technician is responsible for understanding, maintaining, and repairing steam and high purity water generation equipment/components within the manufacturing facility.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Operate, maintain, and repair site Utilities systems, including Boilers, Fire Suppression systems, Potable Water distribution systems, Steam &amp; Condensate distribution &amp; return, Oil-Free Process Air systems, Water Softeners, Ozone Generators, Clean Steam Generators, and other Utilities equipment.</li>\n<li>Complete scheduled maintenance orders ensuring adherence to CMMS metrics. Repair and maintain utility piping, quality water generation equipment, boilers, water filtration systems, steam, and compressed air networks. Ensure all systems are maintained in compliance with EHS and GMP standards.</li>\n<li>Perform routine checks, take samples, log data and complete required documentation in line with procedures. Troubleshoot and repair mechanical equipment including pumps, motors, valves, and liquid transfer systems.</li>\n<li>Maintain equipment, tools, logbooks, PPE, and documentation in a safe, calibrated, and GMP-compliant manner. Report abnormal incidents, near misses, and quality issues promptly to relevant stakeholders.</li>\n<li>Assure all documentation (logbooks, permits, work orders) is complete and accurate. Stay current with all required GSK site, EHS, Regulatory and Global training.</li>\n</ul>\n<p><strong>Basic Qualifications:</strong></p>\n<ul>\n<li>1-3 years of experience working as a mechanical technician in an industrial or regulated manufacturing environment.</li>\n<li>High School diploma or equivalent, such as Trade School graduate, Military, or Vocational-Technical school training.</li>\n<li>Experience with quality process and utilities systems.</li>\n<li>Basic computer skills (Microsoft Suite, Outlook, Intranet, etc.).</li>\n<li>Ability to troubleshoot and a general mechanical aptitude.</li>\n</ul>\n<p><strong>Preferred Qualifications:</strong></p>\n<ul>\n<li>Associate degree, trade certification, boiler operator, instrumentation, or bachelor’s degree with previous experience with Computerized Maintenance Management Work Order Systems (CMMS).</li>\n<li>Experience in regulated manufacturing environments or with high-purity water and clean utilities.</li>\n<li>Strong communication skills and a collaborative approach to teamwork.</li>\n</ul>\n<p><strong>Work arrangement:</strong></p>\n<ul>\n<li>This role is on-site at a GSK facility in the United States.</li>\n<li>The role will include rotating on-call duties and occasional overtime for emergencies, plant projects, or other time-sensitive activities.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Marietta/Plant-Utilities-Technician_447805","directApply":true,"hiringOrganization":{"@type":"Organization","name":"GSK","sameAs":"https://www.gsk.com","logo":"https://logos.yubhub.co/gsk.com.png"},"x-apply-url":"https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Marietta/Plant-Utilities-Technician_447805","x-work-arrangement":"onsite","x-experience-level":"entry","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Asset Life Cycle Management","Data Integrity","Digital Fluency","GxP Regulations","Lean Management","Manufacturing Technologies","Pharmaceutical Manufacturing","Problem Solving","Risk Awareness","Standards Compliance"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-29T05:13:59.662Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Pennsylvania - Marietta"}},"employmentType":"FULL_TIME","occupationalCategory":"Facilities & Maintenance","industry":"Healthcare","skills":"Asset Life Cycle Management, Data Integrity, Digital Fluency, GxP Regulations, Lean Management, Manufacturing Technologies, Pharmaceutical Manufacturing, Problem Solving, Risk Awareness, Standards Compliance"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_1d6e5449-c85"},"title":"Quality Technical and Validation Manager","description":"<p>We are seeking a Quality Technical and Validation Manager to join our team. As a key member of the site quality leadership team, you will be responsible for ensuring the highest standards of GxP compliance in the validation and qualification of processes, equipment, and systems within GSK&#39;s manufacturing and analytical environments.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Provide GxP oversight of validation and qualification activities</li>\n<li>Determine phase-specific controls and ensure their adherence for production and laboratory value streams</li>\n<li>Provide quality oversight and approval of technology transfer activities for new product introductions</li>\n<li>Develop, review, and approve equipment validation protocols</li>\n<li>Determine change control requirements, including for validation and qualification activities</li>\n<li>Ensure that all validation activities are current and conducted in accordance with GSK&#39;s quality standards, regulatory requirements, and industry best practices</li>\n<li>Work with enterprise partners to identify, evaluate, and initiate strategies to rapidly develop product transfers</li>\n<li>Monitor and analyze validation data, identifying trends and areas for improvement</li>\n<li>Participate in internal and external audits and inspections</li>\n<li>Oversee laboratory business applications, methodologies, and automation</li>\n</ul>\n<p>Basic Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree in a relevant scientific or engineering discipline</li>\n<li>10+ years of experience in the pharmaceutical or biotechnology industry</li>\n<li>5+ years of leadership experience</li>\n<li>Experience in developing, approving, and executing process and equipment lifecycle management programs</li>\n</ul>\n<p>Preferred Qualifications:</p>\n<ul>\n<li>Advanced degree in a relevant scientific or engineering discipline</li>\n<li>Strong skills to identify business requirements and provide solutions to complex issues</li>\n<li>Strong knowledge of regulatory requirements and industry standards for validation and quality assurance</li>\n<li>Certification in quality assurance or validation</li>\n<li>Experience with continuous improvement methodologies</li>\n</ul>\n<p>Benefits:</p>\n<ul>\n<li>Comprehensive benefits program, including [insert benefits]</li>\n</ul>\n<p>We value diversity and inclusion in the workplace. We are committed to creating an environment where all employees can thrive and focus on what matters most.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Marietta/Quality-Technical-and-Validation-Manager_431121","directApply":true,"hiringOrganization":{"@type":"Organization","name":"GSK","sameAs":"https://www.gsk.com","logo":"https://logos.yubhub.co/gsk.com.png"},"x-apply-url":"https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Marietta/Quality-Technical-and-Validation-Manager_431121","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["GxP Regulations","Pharmaceutical Regulatory Compliance","Quality Assurance (QA)","Risk Awareness","Technical Writing","Data Integrity","Detail-Oriented","Digital Fluency","Influencing Without Authority","Lean Management","Problem Solving"],"x-skills-preferred":["Advanced degree in a relevant scientific or engineering discipline","Strong skills to identify business requirements and provide solutions to complex issues","Strong knowledge of regulatory requirements and industry standards for validation and quality assurance","Certification in quality assurance or validation","Experience with continuous improvement methodologies"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-29T03:41:40.669Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Pennsylvania - Marietta"}},"employmentType":"FULL_TIME","occupationalCategory":"Manufacturing","industry":"Healthcare","skills":"GxP Regulations, Pharmaceutical Regulatory Compliance, Quality Assurance (QA), Risk Awareness, Technical Writing, Data Integrity, Detail-Oriented, Digital Fluency, Influencing Without Authority, Lean Management, Problem Solving, Advanced degree in a relevant scientific or engineering discipline, Strong skills to identify business requirements and provide solutions to complex issues, Strong knowledge of regulatory requirements and industry standards for validation and quality assurance, Certification in quality assurance or validation, Experience with continuous improvement methodologies"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_da04f7b0-c1c"},"title":"Quality Unit Business Process Specialist","description":"<p>The Quality Unit Business Process Specialist is responsible for quality oversight of SAP processes, business rules, and systems used and the inter-relatedness between each process, rule, or system in order to identify opportunities for improvement and to avoid conflict between processes and systems.</p>\n<p>As a member of the Quality Assurance Operations, this position is co-responsible for the site and the department results. You will act as a Quality Unit Business Process Specialist supporting a United States manufacturing site. You will partner day-to-day with operations, engineering, IT and quality teams to design, implement and sustain quality processes that keep production compliant and reliable.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Act as the Quality Assurance oversight to Production SAP use, business rules, outcomes and compliance including creation of new material master data.</li>\n<li>Key contact for internal departments and other sites for information and assessment and distribution regarding master data.</li>\n<li>Act as site Quality Consultant for SAP when issues arise.</li>\n<li>Act as Quality Assurance oversight of QC Master Data, ensuring adherence to procedures, policies, standards and FDA regulations.</li>\n<li>Demonstrated familiarity and compliance with cGMPs, EHS procedures and regulations, facility regulatory guidelines and standard operating procedures.</li>\n<li>Be SME for local SOPs where SAP is utilized as well as QA approver / compliance authority for QC SOPs relating to QC master data.</li>\n<li>Train users related to SAP business processes.</li>\n<li>Assist with QA Systems objects (including deviations, change controls and CAPA involving SAP use).</li>\n<li>Lead the design, documentation and maintenance of quality unit business processes and standard operating procedures.</li>\n<li>Work with cross-functional teams to translate operational and technical requirements into practical process controls.</li>\n<li>Support change control, risk assessments and quality impact evaluations for process and system changes.</li>\n<li>Contribute to investigations, root cause analysis and corrective and preventive actions to prevent recurrence.</li>\n<li>Monitor quality metrics and trends and recommend process improvements to reduce risk and improve performance.</li>\n</ul>\n<p>Basic Qualifications:</p>\n<ul>\n<li>Bachelor’s degree in life sciences, engineering, quality, or a related technical field.</li>\n<li>3-5 years’ experience in cGMP production or quality control for cGMP manufacturing.</li>\n<li>1-3 years’ experience designing or implementing business processes or SAP systems.</li>\n<li>Practical experience writing or maintaining procedures, work instructions, or process documentation.</li>\n<li>Strong verbal and written communication skills and ability to work on-site with cross-functional teams.</li>\n</ul>\n<p>Preferred Qualifications:</p>\n<ul>\n<li>Experience in biologics or pharmaceutical manufacturing environments with computerized systems or digital manufacturing tools.</li>\n<li>Experience with risk assessment tools and verification of mitigation actions.</li>\n<li>Training or experience in structured root cause analysis methods.</li>\n<li>Proven ability to influence and coach colleagues across functions and levels.</li>\n</ul>\n<p>Work Arrangements: This role is on-site at a United States manufacturing location. Regular presence in production and laboratory areas is required. Hybrid or remote work is not available for this position.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Marietta/Quality-Unit-Business-Process-Specialist_446953","directApply":true,"hiringOrganization":{"@type":"Organization","name":"GSK","sameAs":"https://www.gsk.com","logo":"https://logos.yubhub.co/gsk.com.png"},"x-apply-url":"https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Marietta/Quality-Unit-Business-Process-Specialist_446953","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Data Integrity","Detail-Oriented","Digital Fluency","GxP Regulations","Influencing Without Authority","Lean Management","Pharmaceutical Regulatory Compliance","Problem Solving","Quality Assurance (QA)","Risk Awareness","Technical Writing"],"x-skills-preferred":["Experience in biologics or pharmaceutical manufacturing environments","Risk assessment tools","Structured root cause analysis methods"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-28T08:36:26.769Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Pennsylvania - Marietta"}},"employmentType":"FULL_TIME","occupationalCategory":"Operations","industry":"Healthcare","skills":"Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Influencing Without Authority, Lean Management, Pharmaceutical Regulatory Compliance, Problem Solving, Quality Assurance (QA), Risk Awareness, Technical Writing, Experience in biologics or pharmaceutical manufacturing environments, Risk assessment tools, Structured root cause analysis methods"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_fa09c92a-18e"},"title":"Process Engineer","description":"<p>Join a team dedicated to advancing the manufacturing of drug substances that improve lives. As a Process Engineer, you will develop and optimize processes to make medicines safely and efficiently. You will collaborate closely with cross-functional partners who share a commitment to science, quality, and continuous improvement.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Lead the design, specification, procurement, installation, commissioning, validation, and continued technical support of bioprocess equipment and facility design / operation</li>\n<li>Facilitate multi-disciplined teams in the performance of HAZOPs, FMEAs, process reviews and SOP development efforts</li>\n<li>Act as a primary interface with outside engineering consulting firms on process design projects</li>\n<li>Manage vendors, consultants and contractors to ensure that process and project design and installation are in compliance with cGMP requirements &amp; GSK Bio standards</li>\n<li>Stay current with technical developments in the field of vaccine formulation and manufacturing equipment design, equipment, control technology and GSK-Bio Standards</li>\n<li>Ensure all validation, quality, engineering, safety, and environmental procedures and regulations are met, maintained and documented appropriately</li>\n</ul>\n<p><strong>Basic Qualifications:</strong></p>\n<ul>\n<li>Bachelor’s degree in engineering for a scientific field</li>\n<li>Minimum of 5 + years of experience in process engineering within pharmaceutical or medical device manufacturing</li>\n<li>Experience with Good Manufacturing Practices, Pharma or Vaccine formulation and filling facilities</li>\n<li>Technical understanding of the pharmaceutical industry and engineering practices</li>\n</ul>\n<p><strong>Preferred Qualifications:</strong></p>\n<ul>\n<li>Demonstrated self-direct work habits along with verbal and written communication skills</li>\n<li>Familiarity with regulatory expectations regarding electronic records and electronic signatures</li>\n<li>Experience with process flow design and process optimization techniques</li>\n<li>Proven skills in documentation for compliance and regulatory audits</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Marietta/Sr-Process-Engineer_449687","directApply":true,"hiringOrganization":{"@type":"Organization","name":"GSK","sameAs":"https://www.gsk.com","logo":"https://logos.yubhub.co/gsk.com.png"},"x-apply-url":"https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Marietta/Sr-Process-Engineer_449687","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Asset Life Cycle Management","Data Integrity","Digital Fluency","GxP Regulations","Lean Management","Manufacturing Technologies","Pharmaceutical Manufacturing","Problem Solving","Risk Awareness","Standards Compliance"],"x-skills-preferred":["Spanish"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-19T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Pennsylvania - 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