Night Shift Supervisor – Device Assembly

Job Overview

The Night Shift Supervisor Device Assembly will be a key team member in supporting the start-up and continued success of the Device Assembly Operations at a newly constructed state-of-the-art facility located in North Charleston SC.

The Supervisor will be an established professional with a passion for leading people and functional technical knowledge with manufacturing systems.

Main Responsibilities

• Lead team of technical operators in Medical Device Assembly Operations
• Lead with a Safety-First mindset, proactively enforce all Safety Policies and Procedures
• On-Shift accountability for device assembly component Quality, pro-actively ensure all shift personnel are operating in
• accordance with all pre-established Quality Policies and Procedures
• Enforce strict compliance with current Good Manufacturing Practice (cGMPs) for all direct reports
• Be a Servant-Leader who remains present and available to your direct reports while on shift, maintain active floor
• presence time greater than 75%
• Be a critical and creative thinker who can process complex situations and make informed decisions
• Be a collaborative partner with your on-shift peers in Injection Molding, Metal Component Production, and Warehouse
• Operations
• Ensure constant training compliance of all direct reports, identifying skill gaps and organizing appropriate training
• programs to enhance team performance and capabilities
• Ensure operations and practices comply with established procedures and records
• Ensure in-process tests and inspections are performed in accordance with standard procedures
• Analyze and solve complex operational issues to minimize impact to overall performance of the operation
• Constantly improve technical knowledge of the assembly equipment for which you are responsible
• Support evaluation, specification, installation, and validation of new manufacturing equipment as needed
• Actively support Continuous Improvement functions
• Serve as project member or project leader on improvement programs as needed
• Willing to voluntarily take on additional task and responsibilities, as needed, to ensure the continued success of our
• operation as well as the company at large.
• Perform all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable
• healthcare laws, regulations, and industry codes
• Be a Coachable, Servant Leader, with a results driven mindset, who is able to analyze complex situations, and a confident informed decision maker.
• Review & complete evaluations of eDHR (device history reports)

Skills and Qualification

• Bachelor’s Degree in (Engineering Business, Operations Management) or equivalent experience
• Minimum 5 years relevant industry experience, strongly preferred in high-volume plastic and metal component assembly and production management / assembly automation and inspection technology
• Relevant experience in managing high volume manufacturing, including, material logistics, equipment maintenance and quality management.
• Several years of hands-on manufacturing experience in a 24 / 7 high-volume production setting.
• Proven experience in leading and managing teams in a high-pressure, fast-paced manufacturing environment.
• Passionate & committed self-starter with can do attitude, team player and taking responsibility to get the job done
• Ability to work independent with strong attention to detail and focus on efficiency, effectiveness, and cost.
• Willingness to work from / relocate to Charleston, South Carolina is required.
• Excellent intercultural and interdisciplinary communication skills; Good at building a professional network
• Previous exposure to a highly regulated industry (e.g., medical, pharmaceutical) and knowledge of relevant standards (e.

g., ISO13485, cGMP) is a major plus

• Experience with green field, or startup environment
• Experience within Manufacturing, Medical Device, Pharmaceutical, or Biotechnology industry
• Experience in developing, and implementing new processes or automating current processes.
• Willingness to initially spend an extended period in our facility in Taiwan for induction / training
• Functional knowledge and experience with MES and SAP systems

We Offer

• Competitive compensation package
• Modern working environment with state-of-the-art facilities and technologies
• Challenging assignments in a fast growing and innovative industry
• Position in a dynamic, international team of highly skilled professionals
• Various opportunities for personal and professional development within a global organization

Please note that SHL is a drug free employer. This offer of employment is contingent upon your successful completion of various preemployment screenings, including, but not limited to, a drug test, employment verification, reference checks, and a criminal background check.