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B. Braun Medical Inc. (US)

QC Manager CAPS

B. Braun Medical Inc. (US), Phoenix, Arizona, United States, 85003

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Overview

QC Manager CAPS at B. Braun Medical Inc. (US). Location: Phoenix, Arizona, United States. Functional Area: Quality. Working Model: Onsite. Days of Work: Tuesday, Wednesday, Thursday, Friday, Monday. Shift: 5X8. Relocation Available: Yes. Company: Central Admixture Pharmacy. Requisition ID: 7144. B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets medical products and services. CAPS is part of the B. Braun Group of Companies in the U.S., providing outsourcing admixture services with a national 503B network. For more information about B. Braun Medical, visit www.bbraunusa.com. Position Summary

Responsibilities: Essential Duties Manage the quality control activities of the organization. Oversee tasks associated with inspecting and testing products. Ensure products or services meet quality standards and develop corrective action when needed. Develop, implement, and assess processes and policies designed to test products and services. Monitor and evaluate current testing processes and recommend improvements when necessary. Enforce regulatory compliance. Conduct visual and physical inspections of company products and materials. Monitor the performance of the quality control staff, ensuring the department meets objectives. The job function listed is not exhaustive and may include other responsibilities as assigned by the Supervisor. All employees should maintain safety and health of themselves and others. Expertise: Knowledge & Skills

Advanced knowledge of the professional field and industry; influence the development and application of principles, theories, concepts; determine best course of action. Manage entry to intermediate level employees of a department or function with 1-2 sections; ensure budgets, schedules, and performance requirements are met. Judgment required to resolve complex problems based on experience. Regular contact with department supervisors, leads, subordinates, and peers; frequent contact with external contractors/vendors. Expertise: Qualifications

Required: Bachelor's degree required. 6-8 years related experience required. Regular and predictable attendance. Occasional business travel; cGMP experience/training; aseptic processing training/experience desired. Schedule:

Monday - Friday, 7:30am - 4:00pm, with additional hours as needed. Holidays/overtime as needed. Salary:

$98,483 - $123,096/year. Work Details

Physical requirements: sit/stand, use hands, reach; may lift up to 20 pounds. Work environment includes production/manufacturing, lab, and office settings with moderate noise. Reasonable accommodations may be made for disabilities. Other Duties and Legal

The preceding functions are examples of work performed by employees in this position. Management reserves the right to modify assignments. We are an equal opportunity employer. Know Your Rights: Workplace Discrimination is Illegal. Compensation and Job Attributes

Compensation details: 98,483 - 123,096 Yearly Salary. Seniority level: Mid-Senior level. Employment type: Full-time. Job function: Quality Assurance. Industry: Medical Equipment Manufacturing. Relocation: Yes. Location: Phoenix, AZ. Onsite work model and 5X8 shift.

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