Job Description:

We are looking for a Quality Control Lab Supervisor to join us at medmix, at our new Greenfield Site outside of Atlanta, Georgia USA. This exciting opportunity will allow you use your skills to identify areas of improvement and propose recommendations to management. You will lead and drive the implementation of your recommendations and assess its impact to the business. If you are eager to learn, strive for personal development, are highly motivated and organized, and a great communicator, you can help us drive medmix to the next level.Find out if this opportunity is a good fit by reading all of the information that follows below.Job Description/ Job purposeResponsible for managing incoming, in-process and final inspections for the manufactured product(s) within the Quality Control laboratory.Main Accountabilities and tasksResponsible for managing the quality control lab activities of incoming inspections, in-process inspections and final release activities.Provide Quality oversight at the - Georgia facility, inclusive of site Quality Control laboratory and site Quality Assurance responsibilities.Knowledge and Skill Requirements/Specialized Courses and/or Training:Strong leadership skills and ability to collaborate effectively with team members and stakeholders.Familiarity with quality control concepts, test methods, equipment and applicable national standards relating to testing (i.e. ASTM standards, etc.)Familiarity with applicable federal, , FDA and ISO standards/guidances.Proficiency in the use of PC and programs, particularly Excel, Word (or equivalents if changed by the Company), SAP.Ability to define problems, collect data, establish facts, and draw valid conclusions.Ability to verbally communicate ideas and issues effectively to other team members and management.Ability to write and record data and information as required by procedures.QualificationsWork Experience: 0-2 years of experience manufacturing in a quality environment.Education: Bachelor's degree in related fieldOther:Knowledge of ISO standards is a must.3-4 years of experience using quality management tools.Experience in developing and conducting employee training programs is preferred.Qualification/Certification as an Internal Auditor preferred.Proficiency in the use of personal computers, especially word processing software, spreadsheets, presentation, and database software.Ability to learn quickly and maintain the Quality Assurance metrics.Knowledge of ISO standards or the ability to quickly learn and retain knowledge as required for system compliance.Ability to perform work accurately and thoroughly and to work independently with minimal supervision.Must be organized and can follow a systematic method of performing tasks and the ability to organize and direct a project to completion.Ensures manufacturing and quality documentation is accurate, maintained, and reflects GMP, procedural and regulatory requirements.Must be self-directed and motivated to optimally utilize the available time to organize and complete expected work within given deadlines and reasonable work schedules.Communication skills, both oral and written, as required to communicate effectively with others at all levels in the organization and to provide clear and concise reports and policies as needed. Ability to effectively present information publicly.Ability to work well with subordinates, peers, and superiors in all departments.