FINAL RELEASE SPECIALIST II - 2ND SHIFT: \$22.60-\$31.00/HR + 10% SHIFT DIFFERENTIAL, VulcanForms (Devens, MA) VulcanForms was founded to develop the world?s first industrially scalable laser metal additive manufacturing solution. The company builds and operates advanced digital infrastructure combining scalable additive manufacturing, precision machining, and proven industrial craftsmanship to support aerospace, defense, medical, and other essential industries. About the Role: Support batch final release processes by assembling, reviewing, and completing manufacturing records and documentation in accordance with standard operating procedures, regulatory requirements, and applicable quality standards. Review Device History Records, batch records, technical documentation, and final release records to ensure completeness, accuracy, and compliance. This is an on-site, 2nd shift position in Devens, MA. Hours: Monday through Friday, 3:00 PM to 11:00 PM. Key Responsibilities: - Maintain the flow of work, including setup and review of technical records and inspection documentation - Assign and track work-in-progress records through completion - Attend weekly planning meetings as the Quality Assurance representative - Collaborate with Operations, Customer Service, Distribution, Engineering, Program Management, and other departments to meet customer commitments - Use ERP and electronic Quality Management System (QMS) platforms to manage records and workflow - Identify and initiate nonconformances, deviations, and other quality events - Review data entry, documentation, technical records, and final release records for accuracy and compliance - Ensure each batch is inspected according to specifications and that physical product is verified before final disposition - Review and complete records in accordance with standard operating procedures, agency requirements, accreditation standards, and regulations - Communicate with appropriate personnel regarding missing documentation and required corrections - Report quality assurance variances, errors, and deviations to the Quality Assurance Department - Organize the flow of records through Final Release and coordinate priorities and turnaround times with Program Managers - Develop and release controlled work instructions for the Final Release process - Identify opportunities to improve the Final Release process and its supporting inputs - Work with area stakeholders to resolve issues and maintain strong cross-functional relationships - Perform other duties as assigned by the Manager or Director Qualifications: - 3+ years of experience in medical device manufacturing with direct responsibility for Final Release or Document Control - Proficiency reading and interpreting engineering drawings, blueprints, and technical specifications - Demonstrated experience reviewing Device History Records (DHRs) and batch records for completeness and compliance - Experience initiating, documenting, and tracking nonconformances, deviations, and CAPAs through closure - Strong attention to detail and ability to manage multiple records, priorities, and deadlines - Knowledge of quality systems, manufacturing documentation, and regulated production environments - Strong written and verbal communication skills - Ability to work independently and collaborate effectively within a team Compensation: - Hourly Range: \$22.60 - \$31.00 / hr + 10% second shift differential *Actual compensation is based on skills, qualifications, and experience. VulcanForms offers competitive pay, equity, and comprehensive benefits including medical, dental, vision, life insurance, generous paid time off, and a 401(k) plan with company match.