Quality Supervisor

SUMMARY  The Quality Supervisor drives continuous improvement across Production and related departments through oversight of the Quality Inspector team, identifying and facilitating process improvements, and coordinating Continuous Improvement activities across departments.    ESSENTIAL FUNCTIONS  Build Quality Inspector capabilities through guidance and mentoring  Supervise the Quality Inspector team across shifts, including scheduling and fill-in as needed  Develop deploy and manage training and training plans for Quality Inspectors  Translate best practices and process improvements into daily operations to drive cultural change and overall results  Administer RedZone software including password resets, new products, GMP walks, creating data sheets and triggers, etc.  Orchestrate and facilitate process improvements across all functional areas  Identify and correct inconsistencies in GMP processes and safety procedures  Lead interdepartmental investigations including deviation and CAPA.

Develop and implement of corrective action plans  Conduct root cause analysis, troubleshoot manufacturing issues and create process documentation  Participate in interdepartmental meetings and partner with cross-functional teams to drive a continuous improvement culture  Ensure that quality systems are managed, implemented and maintained throughout the organization  Ensure review and completion of production batch records during production; review for accuracy, completeness and good documentation practices at each step    ADDITIONAL DUTIES  Additional duties as assigned  Perform the duties for the first year of :

• Quality Inspector – Shift One  Lab Tech / Sampler    SUPERVISORY / BUDGET  Day to day supervision of Quality Inspector team including training, coaching, development, evaluation and scheduling  REQUIREMENTS   Education / Experience :     BA / BS in a scientific discipline or equivalent education / experience; graduate degree preferred  Four years' in Quality Assurance and / or manufacturing experience in food, dietary supplement, or other regulated industry  One year supervisory experience in a manufacturing setting  Continuous improvement and / or project management experience preferred  Knowledge / Abilities / Skills :   Strong knowledge of cGMPs in a regulated industry  Strong knowledge of regulatory requirements for the manufacturing of food, beverage, dietary supplements, or Over-the-Counter (OTC) drugs, dietary supplements (21 CFR part 111) preferred.  Strong current knowledge of Quality Assurance methodologies  Demonstrated ability to supervise and develop staff  Knowledge of continuous improvement methodology preferred  Must be flexible to supervise the Quality team across all shifts  Self-starter requiring limited task supervision  Able to collaborate, influence and work effectively across multiple departments  Able to independently solve problems and make decisions based on company and / or quality policy  Ability to read, interpret and apply quality standards, SOP’s, specifications and work instructions  Strong data gathering, metrics development, and report generation skills  Strong analytical and problem-solving skills  Strong organization and detail skills  Strong verbal and written communication skills  Strong interpersonal skills  Commitment to and ability to demonstrate TM’s Company values : humility, respect, quality, collaboration, innovation and sustainability    Technical Skills :   Intermediate MS Office skills  Strong Quality Management System knowledge and skills  Experience with Quality and Manufacturing software platforms preferred (i.e.

RedZone, Master Control Qx and Mx modules)  ERP systems preferred    Travel Requirements :

Approximately 10% thereafter which may include international travel    Work Environment :