11 дней назад
Supervisor, Final Release - Day Shift (Manufacturing Quality)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Supervisor, Final Release - Day Shift (Manufacturing Quality): Leading final release operations for regulated manufacturing products with an accent on documentation accuracy, quality compliance, and production coordination. Focus on supervising records review, inspections, nonconformances, CAPAs, and cross-functional resolution of release issues.
Location: Devens, Massachusetts; five days on-site, Monday through Friday, 7:00 a.m. to 3:00 p.m.
Company
develops and operates vertically integrated 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 daily priorities, monitor performance, and coordinate staffing.
- Oversee manufacturing and technical records through review, inspection, completion, and final disposition.
- Ensure accurate review of data entry, manufacturing documentation, Device History Records, batch records, and final release documentation.
- Coordinate correction of incomplete or inaccurate records and escalate quality variances, deviations, nonconformances, and operational issues.
- Represent Quality and Final Release in production planning meetings and communicate release status, risks, and documentation gaps.
- Improve workflows, work instructions, training, operational metrics, and Final Release turnaround time.
Requirements
- At least 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 Device History Records, batch records, manufacturing records, or similar controlled documentation.
- Experience identifying, documenting, and tracking nonconformances, deviations, or CAPAs.
- Ability to interpret engineering drawings, blueprints, technical specifications, work instructions, and controlled documentation.
- Working knowledge of Quality Management Systems 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.
- Medical, dental, vision, and life insurance.
- Generous paid time off.
- 401(k) plan with company match.
- Competitive salary and equity package based on skills, qualifications, and experience.
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