This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
Job description
SUMMARY
The Quality Supervisor supervises Quality staff in their day-to-day responsibilities. Ensures in-process quality functions are executed, and manufacturing operations are in compliance with company policies, procedures, and applicable cGMP requirements. Ensures timely disposition of incoming ingredients, component, blends, and finished goods. This position also ensures lab activities are compliant, accurate and documented.
ESSENTIAL FUNCTIONS
Supervise day-to-day activities and training of Quality department personnel including quality inspectors and laboratory personnel.
Ensure timely and accurate inspection, testing and disposition of QC samples (e.g., components, ingredients, blends, finished products, pre-ship samples, retest materials, R&D materials)
Ensure all lab instrumentation/equipment is functioning properly, validated for use, and appropriately scheduled for preventative maintenance and calibration
Lead OOS investigations with focus on identifying root causes and taking corrective action where appropriate; document and communicate non-conformances to stakeholders
Ensure accuracy and completeness of documentation (e.g., batch records, evaluation forms, deviations, NCMRs, Corrective Actions, including electronic/digital records)
Partner with Production, Research & Development, Procurement and Planning, and other departments to understand production or corporate priorities and adjust personnel and department priorities as needed
Ensure that processes and methods utilized in the laboratory are compliant and accurate
Ensure that department personnel are properly trained and qualified to perform their job
Ensure compliance with current company, departmental and regulatory requirements
Ongoing assessment of facility operations considering continuous improvement
Assists and performs data collection and analysis of QC metrics
Generates or revises controlled documents such as SOPs and data forms
Lead for special projects as assigned
Perform maintenance, data entry, and analysis in various electronic systems utilized by the company
Perform Quality Inspector duties as backup when needed
Site QMS systems subject matter expert (e.g. Redzone, Master Control, Ignition, etc.)
Other duties as assigned
SUPERVISORY/BUDGET
Direct supervision of Quality department inspectors and lab technicians
No direct budgetary oversight
REQUIREMENTS
Education and Experience:
BA or BS in scientific discipline or equivalent education/experience
Two years' Quality experience in a regulated industry
Four years’ hands-on QC or analytical chemistry experience in a regulated industry
2+ year supervisory experience in a comparable setting
Project management experience preferred
Knowledge/Abilities/Skills:
Strong knowledge of cGMP requirements and quality systems within a regulated industry, such as food, dietary supplements, cosmetics, or pharmaceuticals, required. Knowledge of regulatory requirements for dietary supplements (21 CFR Part 111) preferred.
Technical proficiency in analytical methodologies
Strong knowledge of laboratory protocols and equipment
Demonstrated ability to manage and develop staff
Able to collaborate, influence and work effectively across multiple departments
Ability to read and interpret regulatory documents
Able to independently solve problems and make decisions based on company and/or quality policy
Ability to effectively manage competing priorities with the drive and ability to meet deadlines
Excellent organization skills and attention to detail
Strong verbal and written communication skills
Commitment to and ability to demonstrate TM’s Company values: humility, respect, quality, collaboration, innovation and sustainability
Pay Range
Pay Range: $34.00 - $41.00
Technical Skills
Intermediate MS Suite
WMS/ERP systems preferred
Travel Requirements
Occasional travel to California or 3rd party test labs or supplier(s)
Work Environment
Works often in the QC laboratory with hazardous chemicals present, requiring competence and familiarity with safe handling and storage of acids, bases and solvents.
Works often in production area(s)warehouse, must follow GMP requirements and safety precautions for each area.
Traditional Medicinals, Inc. and its subsidiaries are proud equal-opportunity employers. We wholeheartedly embrace authenticity, diversity, and people’s differences. We acknowledge, celebrate, and support individuality to the great advantage of our consumers, our stakeholders, our products, and the planet. We are committed to building an inclusive workplace for all our people.
We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
#J-18808-Ljbffr
Worksite address
rocky mount, VA, 24151, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.