Quality Control Supervisor
Branch Medical Group
At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible.
Branch Medical Group, a subsidiary of Globus Medical Inc., manufactures a wide range of implants for spinal and orthopedic applications as well as design the instrumentation cases that house them. Our passion, combined with Globus' world-class engineering, transforms clinical insights into tangible musculoskeletal solutions. We are constantly in pursuit of better patient care and understand that speed is critical because life cannot wait.
Essential Functions:
- Direct and supervises the Quality inspection functions within the manufacturing facility.
- Supervises the activities of employees in Quality and ensures compliance to procedures.
- Ensures purchased materials and manufactured products conform to specifications and quality standards.
- Confers with purchasing, customers, and vendors regarding specifications, errors, problems, complaints, compliance with government regulations, international standards and company requirements.
- Oversees quality control inspections on incoming materials and manufactured products.
- Manages and dispositions non-conforming material as part of MRB.
- Provides resources to addressing customer complaint investigations.
- Performs annual performance assessments of direct reports.
- Assists with equipment qualification on new inspection equipment.
- Assists Manufacturing and Engineering in implementation of new procedures, equipment, and methods as related to quality of product and cost reduction.
- Assists Manufacturing, and Engineering in identifying quality requirements and problems for the improvement and establishment of new and existing products, procedures, processes and methods.
- Provides resources for periodic vendor and internal audits to ensure system conformance, effectiveness and accuracy.
- Identifies, develops, and provides training for Quality Assurance staff, for Production Planning and Control, and Manufacturing as needed, as related to Quality Control norms.
- Provides support and expertise in the implementation and enforcement of ISO 13485, ISO 14971 and FDA Quality System Regulation.
- Communicates and support facility quality objectives.
- Helps to establish, follow, and improve company procedures.
- Provides written and oral reports to others to keep them informed of activities and results.
- Maintains a cooperative and motivational attitude with co-workers.
- Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies
- Ensures Compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role
- Represents the company in a professional manner and uphold the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties
- Strongly prefer education level of bachelors' degree (science or engineering preferred) with a minimum experience of as follows,
- Minimum 2 years of experience leading others.
- Minimum 2 years inspection experience in a manufacturing environment in Quality Control or Quality Assurance roles with GMP and SOP's to ISO standards. Preferring that inspection experience to be with a manufacturer of medical devices or similar environment of small lot CNC machining, 3D printing, various assembly and finishing processes.
- 4 years related experience in another manufacturing and FDA-regulated sector.
- Or education level of Masters with 2 years related experience.
- Automated inspection system experience is a plus.
- Computer proficiency with MS Office and statistical analysis tools is required. Solid knowledge of statistical process control theory, application, and calculation is required.
- Ability to use standard measuring equipment (i.e. Micrometers, Calipers, Height Gages, profilometer, ring, plug and thread, go no/go gages, dial indicator, surface plate, gage blocks and torque wrench) is required. Ability to read and interpret engineering drawings for medical devices, including Geometric Dimensioning and Tolerancing (GD&T) is required.
- Attention to detail
- Self-starter
- Advanced critical thinking and problems-solving skills
- Required to sit; climb or balance; and stoop, kneel, crouch or crawl.
- Required to regularly lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds.
- Required to possess specific vision abilities, including close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus.
- Passionate about Innovation : Improving patient care by delivering advanced technology to our customers is at the core of what we do. We are passionate in our role in improving the lives of patients by continuously developing better solutions.
- Customer Focused : We listen to our customers' needs and respond with a sense of urgency.
- Teamwork : Working together, anything is possible. We value every person on our team and treat each other with respect. We are accountable to one another and support each other. Together, we make each other stronger.
- Driven : We pursue our mission with energy and passion. We are nimble, results-oriented and decisive. We overcome obstacles that arise in our quest to deliver solutions that will improve the lives of our customers and patients.
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