Job summary
Job post source
This job is directly from Argon Medical Devices, Inc.
Job overview
The Production Supervisor, 2nd Shift at Argon Medical Devices oversees the molding production team to ensure timely, high-quality product output and compliance with regulatory standards.
Responsibilities and impact
The supervisor manages daily department activities, schedules resources to meet production goals, ensures safety and quality compliance, provides training and coaching, manages employee performance, and assists in budget development.
Experience and skills
Requires AA/AS with 4 years or BA/BS with 2 years of direct supervisory experience in an industrial setting, knowledge of medical components, ISO/cGMP, FDA regulations, and strong analytical and multitasking skills.
Work environment and culture
Argon Medical Devices values a mission-driven, family-oriented culture focused on quality, safety, and continuous improvement in a collaborative environment.
Company information
Argon Medical Devices is a global manufacturer of specialty medical products for interventional procedures, headquartered in Plano, Texas, known for best-in-class products improving patient outcomes.
Team overview
The candidate will lead the weekend shift molding production team at the Wheeling, IL manufacturing facility, managing all production employees in the department.
Job location and travel
The position is based at the Argon Medical manufacturing facility in Wheeling, Illinois, near Chicago, working the 2nd shift including weekends.
Unique job features
The role involves leadership in a regulated medical device manufacturing environment with a focus on safety, quality, and continuous improvement, directly impacting patient care products.
Company overview
Argon Medical Devices Inc. is a global manufacturer of specialty medical products, focusing on devices used in interventional procedures, vascular surgery, and oncology. They generate revenue by selling a diverse range of medical devices, including biopsy needles, drainage catheters, and vascular access products, to hospitals, clinics, and healthcare providers worldwide. Founded in 1972, Argon has a history of innovation and growth, marked by strategic acquisitions and a commitment to improving patient outcomes through high-quality, reliable medical solutions.
How to land this job
Position your resume to highlight your supervisory experience in industrial or manufacturing environments, emphasizing your ability to manage production teams and meet production goals under strict regulatory standards like ISO 13485 and FDA compliance.
Emphasize your skills in resource scheduling, safety program implementation, and continuous improvement initiatives that align with Argon Medical Devices' focus on quality and patient outcomes.
Apply through multiple channels including Argon Medical Devices' corporate careers page and LinkedIn to maximize your visibility and ensure your application is received.
Connect with current production supervisors or managers at Argon Medical Devices on LinkedIn, initiating conversations by complimenting their leadership in manufacturing or asking about the challenges and innovations in medical device production on the 2nd shift.
Optimize your resume for ATS by incorporating keywords from the job description such as 'production supervision,' 'cGMP compliance,' 'ISO 13485,' 'safety programs,' and 'resource scheduling' to improve your chances of passing automated screenings.
Use Jennie Johnson's Power Apply feature to automate tailored applications, find multiple job posting sources, and identify relevant LinkedIn contacts, allowing you to focus your energy on preparing for interviews and networking effectively.
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