What are the responsibilities and job description for the Production Supervisor position at Johnson & Johnson?
Mentor Worldwide, LLC, a member of Johnson & Johnson's Medical Devices Companies, is currently recruiting for a Production Supervisor to be located in Irving, TX
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 https://www.jnj.com/.
Mentor is a leading supplier of breast implants in the global aesthetic market. The company develops, manufactures, and markets innovative, science-based products for surgical and non-surgical medical procedures that allow breast surgery patients to improve their quality of life. The company is focused on two strategic areas: breast reconstruction and breast augmentation. MENTOR® is the only manufacturer whose silicone breast implants are made in the U.S.A. For over 20 years, more than 5 million women have chosen MENTOR® Breast Implants.
Are you interested in joining a diverse team that is helping improve patient care and drive innovation? Apply today for this exciting opportunity!
The Production Supervisor is responsible for day-to-day operations within assigned medical device manufacturing area, leading production personnel to improve quality and output in a manufacturing operation.
Key Responsibilities
EXPERIENCE AND SKILLS:
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 https://www.jnj.com/.
Mentor is a leading supplier of breast implants in the global aesthetic market. The company develops, manufactures, and markets innovative, science-based products for surgical and non-surgical medical procedures that allow breast surgery patients to improve their quality of life. The company is focused on two strategic areas: breast reconstruction and breast augmentation. MENTOR® is the only manufacturer whose silicone breast implants are made in the U.S.A. For over 20 years, more than 5 million women have chosen MENTOR® Breast Implants.
Are you interested in joining a diverse team that is helping improve patient care and drive innovation? Apply today for this exciting opportunity!
The Production Supervisor is responsible for day-to-day operations within assigned medical device manufacturing area, leading production personnel to improve quality and output in a manufacturing operation.
Key Responsibilities
- Accountable for achieving production targets while maintaining cost controls.
- Work with team members to establish department goals and objectives and identify appropriate key performance measurements and supervise progress in each area.
- Champion process improvement teams and manage the challenges which may impact production and implement innovation that improve production capabilities.
- Collaborate with Supply Chain Partners (i.e., Production Planning, Manufacturing Engineering, Quality, etc.), to deliver safe, reliable, high-quality products for our patients at a reasonable cost.
- Responsible for overall manufacturing of existing and newly developed products in compliance with all regulatory and QSR requirements in an efficient manner and in accordance with planned budget.
- Sets the standards for performance assessment and feedback, effective communication, promoting positive morale and supporting employee involvement programs.EDUCATION:
- Bachelor's Degree required
EXPERIENCE AND SKILLS:
- Minimum 2 years of relevant work experience
- Experience within a GMP and/or ISO regulated manufacturing environment
- Solid computer skills, including Windows and Microsoft Office software experience
- Excellent written and verbal communication skills
- People leadership/management experience (direct or indirect reports)
- Experience with ISO9001 or ISO13485
- Experience with NCR process, CAPA, and other quality system components
- Lean/Six Sigma/Process Excellence Tools and methodologies experience, training, or certification
- General knowledge of capacity planning including ERP and Manufacturing Processing Systems (MPS)
- Proven experience revising site documentation to improve operations (logbooks, process sheets, work instructions, training guides, etc.)
- Demonstrated strong project/initiative management skills and the ability to lead and facilitate project improvements
- Requires ability and flexibility to work operational hours of Sunday Through Thursday, 9:30 PM to 5:00 AM and provide support on the weekends or other shifts as needed
- Requires up to 10% domestic travel
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