Quality Inspection Supervisor - 2nd Shift

Description

Johnson & Johnson is currently seeking a Quality Production Supervisor - 2nd Shift to join Abiomed's Quality team based in Danvers, MA.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at

Principle Duties:

• Establish a culture of excellence in execution, continuous improvement, and communication
• Lead a Quality Inspection team (process, material, and equipment) to meet and exceed targets related to people, safety, environment, quality, delivery, and cost
• Coordinate inspection activities with purchasing, maintenance/facilities, engineering, Supplier Engineering and Quality Assurance team to optimize team members, schedules, and inspection equipment.
• Establish and manage cross training models for their area.
• Engage with engineering team to utilize capacity models and assess constraints as projected demand changes
• Perform administrative duties such as regular employee meetings, timekeeping/attendance/vacation requests, performance appraisals disciplinary actions, interviewing, rewards & recognition, training, and development.
• Manage inspection and deliveries to target levels by cross loading resources across quality inspection to meet production build requirements
• Assist Quality Inspection Manager by providing data and analysis on inspection backlog, touch time, department goals and operational issues to determine causes of non-conformities
• Help identify and work with Supplier Quality Engineering to resolve inspection problems. Ability to know when to escalate an issue.
• Ensure compliance to the training plans, procedures, and industry regulations.
• Support and drive lean principles throughout the Quality inspection and MRB

Qualifications

• Associate degree required, or equivalent years of experience
• 2 years supervisory experience. Medical device experience preferred
• Minimum 6 years related experience in a Manufacturing environment
• Minimum 2 years related experience in a Quality inspection environment preferred
• Quality Assurance experience & knowledge of GMP required
• Knowledge of Lean, Kaizen, and Continuous Improvement initiatives
• Ability to gain cooperation of others and lead team members
• Ability to communicate ideas and information clearly, effectively, and frequently (oral and written).
• Proficient in Microsoft Office Suite. Working knowledge of SAP desired.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit