Job summary
Job post source
This job is directly from Argon Medical Devices as explicitly stated that they are not leveraging search firms.
Job overview
The Production Supervisor, 2nd Shift at Argon Medical Devices oversees the molding department's weekend shift, ensuring timely production of high-quality medical products while maintaining compliance with industry standards.
Responsibilities and impact
The supervisor manages daily activities of production employees, schedules resources to meet production goals, enforces safety and quality standards, provides training and coaching, implements safety programs, leads the team, and assists in budget management.
Experience and skills
Requires AA/AS with 4 years or BA/BS with 2 years of direct supervisory experience in an industrial environment, knowledge of medical components, ISO/cGMP and FDA regulations or equivalent training, and strong analytical and multitasking skills.
Work environment and culture
Argon Medical Devices values a family-oriented culture united by a mission to improve patient outcomes and emphasizes safety, quality, and continuous improvement.
Company information
Argon Medical Devices is a global manufacturer of specialty medical products headquartered in Plano, Texas, known for best-in-class products in interventional radiology, vascular surgery, cardiology, and oncology.
Team overview
The candidate will manage the weekend shift team of operators in the molding department, providing leadership and coaching.
Job location and travel
The position is based at the manufacturing facility in Wheeling, Illinois, near Chicago.
Unique job features
The role involves leadership in a regulated medical device manufacturing environment with a focus on compliance with ISO/GMP/FDA standards and continuous improvement.
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
Tailor your resume to highlight supervisory experience in production environments, emphasizing your ability to manage second shift operations and weekend teams, as this is central to the Production Supervisor role at Argon Medical Devices.
Focus on showcasing your knowledge and practical application of ISO 13485, cGMP, FDA regulations, and safety compliance, as these are critical for ensuring quality and regulatory adherence in medical device manufacturing.
Apply through multiple channels including Argon Medical Devices' official corporate careers page and LinkedIn to maximize your visibility and increase your chances of getting noticed for this role.
Connect with current Argon Medical Devices employees in the manufacturing or production supervision divisions on LinkedIn; when reaching out, you can break the ice by mentioning your interest in their commitment to quality and safety or by asking about their experience managing second shift operations.
Optimize your resume for ATS by incorporating keywords from the job description such as 'production supervision,' 'ISO 13485,' 'cGMP,' 'FDA compliance,' 'safety programs,' and 'team leadership' to ensure your resume passes initial automated screenings.
Utilize Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application portals, and find relevant LinkedIn contacts to network with, allowing you to focus more on preparing for interviews and refining your qualifications.
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