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Quality Supervisor

Traditional Medicinals

Rocky Mount, Virginia • Today

Full-time

USD 34.00 - 41.00 per hour

Audit IT Supervisor

Sysco Corporation

Remote • Today

Full-time

USD 104,200.00 - 156,400.00 per year

Job Details

Skills

Manufacturing Operations
Training
Inspection
Testing
Instrumentation
Preventive Maintenance
FOCUS
ROOT
Corrective And Preventive Action
Documentation
Evaluation
Research and Development
Procurement
Regulatory Compliance
Continuous Improvement
Data Collection
Forms
Data Entry
Backup
QMS
Master Control
Budget
Business Analytics
Business Analysis
Analytical Chemistry
Supervision
Project Management
Good Manufacturing Practice
Quality Management
Pharmaceuticals
Analytical Skill
Management
Attention To Detail
Communication
TM
Collaboration
Innovation
Sustainability
WMS
Enterprise Resource Planning
SAFE
Storage
Warehouse
GMP
SAP BASIS
Law
Quality Control
Quality Assurance

Manufacturing Operations
Training
Inspection
Testing
Instrumentation
Preventive Maintenance
FOCUS
ROOT
Corrective And Preventive Action
Documentation
Evaluation
Research and Development
Procurement
Regulatory Compliance
Continuous Improvement
Data Collection
Forms
Data Entry
Backup
QMS
Master Control
Budget
Business Analytics
Business Analysis
Analytical Chemistry
Supervision
Project Management
Good Manufacturing Practice
Quality Management
Pharmaceuticals
Analytical Skill
Management
Attention To Detail
Communication
TM
Collaboration
Innovation
Sustainability
WMS
Enterprise Resource Planning
SAFE
Storage
Warehouse
GMP
SAP BASIS
Law
Quality Control
Quality Assurance

Summary

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: $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.
PandoLogic. Keywords: Quality Control / Quality Assurance Supervisor, Location: Rocky Mount, VA - 24151

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: pandfeed
Position Id: 604128784
Posted 2 days ago

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