11 дней назад
Supervisor, Final Release - Night Shift (Manufacturing Quality)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Supervisor, Final Release - Night Shift (Manufacturing Quality): Leading final release operations for manufactured products, ensuring records, inspections, documentation, and product dispositions meet quality, customer, and regulatory requirements with an accent on controlled manufacturing records, DHRs, batch records, and QMS compliance. Focus on supervising night-shift workflows, resolving documentation and quality issues, tracking nonconformances and CAPAs, and improving release turnaround and accuracy.
Location: Devens, Massachusetts; 5-day on-site role, Monday through Friday, 3:00 p.m. to 11:00 p.m.
Company
develops and operates industrially scalable laser metal additive manufacturing and precision machining capabilities for aerospace, defense, medical, and other essential industries.
What you will do
- Supervise the Final Release team, assign work, set priorities, monitor workflow, and manage daily schedules.
- Oversee manufacturing records, technical records, DHRs, batch records, inspections, and final release documentation.
- Ensure products and batches are verified against specifications before final disposition.
- Identify, document, escalate, and track quality variances, deviations, nonconformances, and CAPAs.
- Coordinate with Operations, Program Management, Engineering, Customer Service, Distribution, and other stakeholders to resolve release issues.
- Maintain operational metrics and support improvements to workflow, documentation quality, training, and turnaround time.
Requirements
- 5+ years of experience in manufacturing, quality assurance, final release, or a related regulated manufacturing environment.
- Experience leading, coordinating, training, or directing employees in a manufacturing or Quality environment.
- Experience reviewing DHRs, batch records, manufacturing records, or similar controlled documentation.
- Experience identifying, documenting, or tracking nonconformances, deviations, and CAPAs.
- Ability to interpret engineering drawings, blueprints, technical specifications, work instructions, and controlled documentation.
- Working knowledge of QMS and ERP systems, with strong attention to detail and cross-functional communication skills.
Nice to have
- Experience in medical device or aerospace manufacturing.
Culture & Benefits
- Inclusive environment focused on quality, curiosity, accountability, ownership, and continuous learning.
- Competitive salary and equity package.
- Medical, dental, vision, and life insurance.
- Generous paid time off.
- 401(k) plan with company match.
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