{"schemaVersion":"jobsearcher.job.v1","id":"bb4f16b5daa13f825d5baa66","url":"https://jobsearcher.com/jobs/bb4f16b5daa13f825d5baa66","canonicalUrl":"https://jobsearcher.com/jobs/bb4f16b5daa13f825d5baa66","title":"Final Release Specialist - 2nd Shift","description":"About Us\nFounded in 2015 to develop the world’s first industrially scalable laser metal additive manufacturing solution, VulcanForms is reshaping how the world manufactures critical products. We build and operate advanced digital infrastructure that enables innovation, accelerates growth, and supports sustainability across aerospace, defense, medical, and other essential industries. Through our vertically integrated capabilities, including scalable additive manufacturing and precision machining, we deliver true end-to-end production at scale by combining cutting-edge technology with a foundation of proven industrial craftsmanship. Our team brings deep expertise in manufacturing, materials science, software, automation, and operations, united by a shared commitment to quality, curiosity, and accountability. We foster an inclusive culture where people take ownership, solve meaningful problems, and continuously learn, because we believe diverse perspectives lead to better outcomes.\n\nJob Purpose\nThe Final Release Specialist II supports the batch final release processes and performs functions necessary to ensure that all relevant manufacturing records and documentation are assembled, reviewed, and completed in a compliant efficient manner. This position requires attention to detail and must be performed in accordance with standard operating procedures, as well as all applicable requirements. This is a second shift role with the hours of Monday through Friday, 3pm - 11pm.\nKey Responsibilities\nMaintain the flow of work, to include but not limited to, the setup of technical records for review, inspection,\nAssign and track to completion all work in progress (WIP) records.\nAttend weekly planning meeting as the Quality Assurance representative and work with Operations, Customer Service, Distribution, Engineering and all other cross functional departments to ensure commitments and customer needs are met.\nKnowledgeable in ERP and QMS electronic systems\nAble to identify and initiate nonconformances.\nResponsible for the QA review of data entry, documentation, and technical and final release records.\nEnsure that each batch is inspected per specification, physical product is verified prior to setting final disposition.\nReview and complete records ensuring compliance with applicable SOPs, agency requirements and accreditation standards and regulatory regulations.\nCommunicates with appropriate personnel on missing required documentation, error corrections required.\nResponsible for reporting QA variances, errors and deviations on all initiated documentation to Quality Assurance Department.\nOrganizes the flow of records through Final Release, working with Program Managers to prioritize and provide turnaround times.\nDevelops and releases controlled work instructions on the Final Release process.\nIdentifies opportunities for improvement both in the Final Release process and inputs to the Final Release process.\nWorks closely with area stakeholders that are inputs to the Final Release process to resolve issues. Develops strong working relationships and operates in a team structure.\nPerforms other duties as assigned by the Manager and Director of the Department.\nQualifications\n3+ years of experience in Med Device Manufacturing with direct responsibility for Final Release or Document Control.\nProficiency in reading and interpreting engineering drawings, blueprints, and technical specifications.\nDemonstrated experience reviewing Device History Records (DHRs) and Batch Records for completeness and compliance.\nExperience initiating, documenting, and tracking nonconformances, deviations, and CAPAs to closure.\n\nVulcanForms offers a competitive salary and equity package. Actual compensation is based on factors such as the candidate's skills, qualifications, and experience. In addition, VulcanForms provides comprehensive benefits including medical, dental, vision, and life insurance; generous paid time off; and a 401(k) plan with company match.\nThe hourly pay range for this position is $22.60-$31. This role shall also include a pay differential of 10% on any applicable shift not included in the standard base-pay shifts.","company":"Vulcanforms","rawCompany":"vulcanforms","city":"Devens","state":"MA","isRemote":false,"isActive":false,"createdAt":"2026-07-20T00:09:37.752Z","occupations":[{"code":"13-1041.07","title":"Regulatory Affairs Specialists","slug":"regulatory-affairs-specialists"},{"code":"29-2072.00","title":"Medical Records Specialists","slug":"medical-records-specialists"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Final Release Specialist - 2nd Shift","description":"About Us\nFounded in 2015 to develop the world’s first industrially scalable laser metal additive manufacturing solution, VulcanForms is reshaping how the world manufactures critical products. We build and operate advanced digital infrastructure that enables innovation, accelerates growth, and supports sustainability across aerospace, defense, medical, and other essential industries. Through our vertically integrated capabilities, including scalable additive manufacturing and precision machining, we deliver true end-to-end production at scale by combining cutting-edge technology with a foundation of proven industrial craftsmanship. Our team brings deep expertise in manufacturing, materials science, software, automation, and operations, united by a shared commitment to quality, curiosity, and accountability. We foster an inclusive culture where people take ownership, solve meaningful problems, and continuously learn, because we believe diverse perspectives lead to better outcomes.\n\nJob Purpose\nThe Final Release Specialist II supports the batch final release processes and performs functions necessary to ensure that all relevant manufacturing records and documentation are assembled, reviewed, and completed in a compliant efficient manner. This position requires attention to detail and must be performed in accordance with standard operating procedures, as well as all applicable requirements. This is a second shift role with the hours of Monday through Friday, 3pm - 11pm.\nKey Responsibilities\nMaintain the flow of work, to include but not limited to, the setup of technical records for review, inspection,\nAssign and track to completion all work in progress (WIP) records.\nAttend weekly planning meeting as the Quality Assurance representative and work with Operations, Customer Service, Distribution, Engineering and all other cross functional departments to ensure commitments and customer needs are met.\nKnowledgeable in ERP and QMS electronic systems\nAble to identify and initiate nonconformances.\nResponsible for the QA review of data entry, documentation, and technical and final release records.\nEnsure that each batch is inspected per specification, physical product is verified prior to setting final disposition.\nReview and complete records ensuring compliance with applicable SOPs, agency requirements and accreditation standards and regulatory regulations.\nCommunicates with appropriate personnel on missing required documentation, error corrections required.\nResponsible for reporting QA variances, errors and deviations on all initiated documentation to Quality Assurance Department.\nOrganizes the flow of records through Final Release, working with Program Managers to prioritize and provide turnaround times.\nDevelops and releases controlled work instructions on the Final Release process.\nIdentifies opportunities for improvement both in the Final Release process and inputs to the Final Release process.\nWorks closely with area stakeholders that are inputs to the Final Release process to resolve issues. Develops strong working relationships and operates in a team structure.\nPerforms other duties as assigned by the Manager and Director of the Department.\nQualifications\n3+ years of experience in Med Device Manufacturing with direct responsibility for Final Release or Document Control.\nProficiency in reading and interpreting engineering drawings, blueprints, and technical specifications.\nDemonstrated experience reviewing Device History Records (DHRs) and Batch Records for completeness and compliance.\nExperience initiating, documenting, and tracking nonconformances, deviations, and CAPAs to closure.\n\nVulcanForms offers a competitive salary and equity package. Actual compensation is based on factors such as the candidate's skills, qualifications, and experience. In addition, VulcanForms provides comprehensive benefits including medical, dental, vision, and life insurance; generous paid time off; and a 401(k) plan with company match.\nThe hourly pay range for this position is $22.60-$31. This role shall also include a pay differential of 10% on any applicable shift not included in the standard base-pay shifts.","datePosted":"2026-07-20T00:09:37.752Z","dateModified":"2026-07-20T00:09:37.752Z","hiringOrganization":{"@type":"Organization","name":"Vulcanforms","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Devens","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"bb4f16b5daa13f825d5baa66"},"url":"https://jobsearcher.com/jobs/bb4f16b5daa13f825d5baa66"}}