Quality Control Supervisor (50363)

Raining Rose; Cedar Rapids (IA); On-site; USD 65,000 - 90,000; Full time

Job summary

Raining Rose in Cedar Rapids, IA is seeking a QA Supervisor to direct daily activities in the Quality department, overseeing testing, release of products, and management of Quality Technicians. The role requires ensuring compliance with FDA regulations and customer requirements while maintaining quality standards.

The ideal candidate will lead by example, enforce GMPs, and collaborate with cross-functional teams to improve processes and product quality in a fast-paced manufacturing environment.

Qualifications

• Bachelor’s degree preferred.
• Minimum 3+ years of management and/or leadership experience.
• Minimum 4+ years in a relatable field.
• Experience with internal audits.

Responsibilities

• Directs and coordinates activities in the Quality department related to testing and releasing quality products and raw materials.
• Supervise Quality technicians including scheduling, development, discipline, and hiring.
• Ensure compliance with FDA CFR and other regulatory requirements for OTC drugs, cosmetics, organic certifications, and customer requirements.
• Approve or reject procedures and specifications impacting product identity, strength, quality, and purity.
• Maintain KPI data and report monthly; collaborate with other departments to improve product quality.

Skills

Strong leadership

Mentor & train team

Planning & organizational skills

Analytical skills

Adaptability in regulated environment

Education

Bachelor’s degree in relatable field

Job description

Job Details

Job Location: Raining Rose - Cedar Rapids, IA 52403

Position Type: Full Time

Education Level: 4 Year Degree

Travel Percentage: None

Job Category: QA - Quality Control

SUMMARY

Directs and coordinates activities concerned with daily task in the Quality department as it relates to the testing and releasing of quality product and raw materials including the management of quality technicians, specification review, material investigation, and regulatory compliance.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.

ESSENTIAL DUTIES AND RESPONSIBILITIES

• Responsible supervising and directing Quality technicians who are responsible for the sampling, inspection, and evaluation of raw material, components, and finished goods at Raining Rose. This includes scheduling, professional development, discipline, and hiring of Quality Technicians.
• Understand and enforce compliance to Code of Federal Regulations (FDA) and other regulatory requirements for products including but not limited to: Over the Counter (OTC) Drugs, Cosmetics, Certified Organic, Certified Gluten-Free, and other Customer requirements.
• Authority to release or reject product after testing and, if needed, after review and investigation.
• Assist with Quality Control testing as needed.
• Assist in the coordination of testing results from 3rd party and internal labs involving finished products, in-process products, and raw materials.
• Analyze facts or circumstances surrounding individual issues to determine what action should be taken within the limits of standard practices. Assist in investigations to determine causes of faulty work or out of specifications (OOS) then consult and advise Production Supervisors as to corrective measures including Corrective and Preventive Action functions.
• Approve or reject procedures and specifications impacting the identity, strength, quality, and purity of products and raw materials.
• Teach and train others on compliance information and safety knowledge to complete tasks.
• Quality Control Supervisor shall report any product issues relating to Quality and Product Safety to Quality Manager and/or Chief Operations Officer while handling the daily duties as they relate to staffing and testing. Quality or Safety issues as needed shall also be directed to the CEO.
• Maintain data and report on department key performance indicators (KPI) monthly.
• Maintain close working relationships with other department leaders and personnel to meet and maintain product quality, identify, solve, and prevent problems affecting product quality, maximize productivity, and comply with regulatory requirements.
• Manage quality control projects and meet set deadlines via independent work and/or interdepartmental collaboration.
• Supervise and manage environmental and water testing on a monthly and quarterly basis.
• Contribute to continuous review and improvement of processes to ensure consistent, efficient, and effective practices. Make suggestions regarding procedures, standards, and equipment to facilitate work and maintain product quality.
• Firm understanding and compliance with company's Good Manufacturing Practices (GMPs)
• Display and promote company values (ASPIRE: Attitude, Safety, Passion, Integrity, Relationship, and Evolve)
• Regular attendance
• Other duties as assigned.

QUALIFICATIONS

• Strong written and verbal communication skills with prevalent professional demeanor
• Ability to mentor, train, motivate, direct, and empower a team.
• Strong leadership skills
• High ethical standards
• Excellent planning and organizational skills
• Ability to develop personnel and equipment structures to support present and future operations.
• Analytical skills to identify and resolve problems in a timely manner.
• Ability to work in a fast paced, rapidly changing, and regulated environment.
• Ability to work effectively across departmental teams.
• Maintain professional technical knowledge.
• Mathematical aptitude
• Proficient in Microsoft Office Suite Products and ability to learn new systems quickly.

EDUCATION AND/OR EXPERIENCE

• Bachelor’s degree in relatable field preferred
• A minimum of 3+ years of management and/or leadership experience required.
• A minimum of 4+ years' experience in a relatable field required.
• Experience with and knowledge of internal audits
• Experience with quoting projects, product cost analysis and ROI analysis preferred.
• Technical writing experience preferred.
• Knowledge of analytical theories required.Knowledge of GMP's, OSHA rules and regulations required.
• Knowledge of material inspection and quality control methods and equipment
• Knowledge of metric and dashboard development preferred.
• Training and understanding of laboratory hazards preferred.

PHYSICAL REQUIREMENTS/ WORKING ENVIRONMENT

The work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Sit an average of 3-4 hours per day.
• Stand an average of 2-3 hours per day.
• Walk an average of 2-3 hours per day.
• Bend/Stoop - Rarely (1-2 times per day)
• Squat - Rarely (1-2 times per day)
• Reach above shoulder level - Rarely (1-2 times per day)
• Crouch - Rarely (1-2 times per day)
• Up to 10 lbs - Occasionally (1-4 times per hour)
• Up to 10 lbs - Occasionally (1-4 times per hour)
• Simple/light grasping (right hand) - Frequently (5-24 times per hour)
• Firm/strong grasping (both hands) - Rarely (1-2 times per day)
• Fine dexterity (both hands) - Constant (more than 25 times per hour)
• Job requires being around moving machinery and equipment.
• Job requires wearing personal protective equipment as necessary.