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Concept Laboratories
Pleasant Prairie, WI | Full Time
$99k-126k (estimate)
6 Days Ago
Concept Laboratories
Pleasant Prairie, WI | Full Time
$104k-136k (estimate)
4 Weeks Ago
Concept Laboratories
Pleasant Prairie, WI | Full Time
$104k-136k (estimate)
4 Weeks Ago
Spectrum Plastics Group, A DuPont Business
Pleasant Prairie, WI | Full Time
$92k-110k (estimate)
4 Weeks Ago
Spectrum Plastics Group, A DuPont Business
Pleasant Prairie, WI | Full Time
$92k-110k (estimate)
4 Weeks Ago
SPECTRUM PLASTICS MASTER
Pleasant Prairie, WI | Other
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Momentum Staffing Group
Pleasant Prairie, WI | Full Time
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Managed Care Staffers
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Quality Assurance Supervisor
Concept Laboratories Pleasant Prairie, WI
$104k-136k (estimate)
Full Time | Durable Manufacturing 4 Weeks Ago
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Concept Laboratories is Hiring a Quality Assurance Supervisor Near Pleasant Prairie, WI

Job DescriptionJob Description Job Title: Quality Assurance Supervisor Department: QA
Reports to: Director of Quality
Note: This position is training at our Chicago office but our business is moving to Pleasant Prairie WI November of 2024. This will be where the position will be at.
Job Summary:The QA Supervisor is responsible for ensuring timely and effective implementation of all company's policies, procedures, and activities involved in assuring the quality of manufactured products. Maintain close working relationships with other department managers and supervisory personnel in
order to meet and maintain product quality, identify, solve, and prevent problems affecting product quality, maximize productivity, and comply with regulatory requirements.
Supervisory Responsibilities:
  • Oversees the daily workflow of the department.
  • Provides constructive and timely performance evaluations.
Duties/Responsibilities:
  • Supervise and direct quality assurance technicians/auditors who are responsible for enforcing cGMP and other quality-related policies in order to meet product quality standards.
  • Perform analytical testing when needed with instrumentation (GC, HPLC, FT-IR, UV-Vis, etc.).
  • Review Production Batch Records and other manufacturing-related documents to verify compliance, integrity and record keeping for all mandated manufacturing processes, quality checks, testing, sampling, and sanitation activities.
  • Assist in the coordination of testing results involving finished products, raw materials, and packaging components and the appropriate release and hold programs associated with these materials.
  • Oversee the “On Hold” product program, including the status, release, and destruction of “Rejected” products.
  • Processes, distributes, and maintains controlled documentation (i.e., SOPs, WI, copacker technical manual, change control tracking, material specification, logbooks, etc.) using a document control system.
  • Assist in the investigation and review of deviations, change controls, CAPAs and OOS reports to assure complete compliant source data.
  • Audit quality control of raw materials, packaging components, labels, and finished products to ensure compliance with established specifications and regulatory standards.
  • Follow up with implemented programs (GMPs, ISO, Cleaning and Sanitation, Pest Control, Equipment Calibration, etc.) to ensure compliance by employees and other personnel in the manufacturing facility.
  • Assist in investigating and correcting quality-related issues (including customer complaints) through collaboration with other departments.
  • Make proactive recommendations and offering/presenting solutions to the Quality Systems & Regulatory Compliance Department Management to improve quality and work efficiency.
  • Assist in the implementation of policies, operating procedures, quality systems and programs which ensure proper testing, evaluation, inspection, and technical support in order to meet product quality standards.
  • Orders supplies, submits purchasing orders, and processes departmental invoices.
  • Assists with internal audits and collecting documentation and tracking during audits.
  • Assists with tracking training completions and uploading of QA training records.
  • Adheres to policies, procedures, SOP's, safe work practices, and safety policies and procedures.
  • Communicates concerns to supervisor, reports hazards, and provides input on prevention.
  • Initiate non-conformance investigations.
  • Demonstrate strong organization skills related to priorities and workload.
  • Compile and communicate performance metrics and data trend analyses to senior management for Batch Review and Release relevant activities.
  • Identify opportunities for improvement within scope of work.
  • Serves as change agent for continuous improvement in operational excellence activities.
  • Provide logistical support and technical knowledge during regulatory and internal inspections of Company quality systems.
  • As needed, other administrative duties may be assigned by the Quality Assurance Management team.
Required Skills/Abilities:
  • Excellent verbal and written communication skills.
  • Analytical chemistry skills, involving instrumentation and method development.
  • Strong mathematical, analytical, and problem-solving skills.
  • Ability to speak and write effectively and strong ability to collaborate with others to complete assigned tasks.
  • Proficient with Microsoft Office Suite or related software.
  • Working Knowledge of cGMP, FDA regulations and ISO standards
  • Excellent organizational skills and attention to detail.
  • Excellent time management skills with a proven ability to meet deadlines.
  • Strong supervisory and leadership skills.
  • Ability to prioritize tasks and to delegate them when appropriate.
  • Ability to function well in a high-paced and at times stressful environment.
  • Ability to learn quickly, work independently, prioritize, and assume responsibility for new tasks in a rapidly growing and changing company.
  • Must be able to work a flexible schedule, including off shifts and weekends as needed.
Education and Experience:EDUCATION and EXPERIENCE: Four (4) year bachelor’s degree in a science field (chemistry, biology, etc.) and a minimum of five (5) years experience in Quality Assurance (preferably cosmetics, biologic, medical device, or pharmaceutical industries).
Physical Requirements: Prolonged periods of sitting at a desk and working on a computer.
Must be able to lift up to 15 pounds at times.
Company DescriptionConcept Laboratories, Inc., a 30-year-old, Chicago based personal care and skincare manufacturer, is looking for an intern to join our e-commerce sales and marketing team for the summer. This position provides a unique opportunity to learn under a team with over fifteen years of combined e-commerce experience while offering hands-on experience in a rapidly growing industry. We have grown tremendously in the past two years and are moving to Pleasant Prairie WI. November 2024. This would require training in Chicago to eventually work in Pleasant Prairie WI at the end of 2024.
Concept Laboratories, Inc., a 30-year-old, Chicago based personal care and skincare manufacturer, is looking for an intern to join our e-commerce sales and marketing team for the summer. This position provides a unique opportunity to learn under a team with over fifteen years of combined e-commerce experience while offering hands-on experience in a rapidly growing industry. We have grown tremendously in the past two years and are moving to Pleasant Prairie WI. November 2024. This would require training in Chicago to eventually work in Pleasant Prairie WI at the end of 2024.

Job Summary

JOB TYPE

Full Time

INDUSTRY

Durable Manufacturing

SALARY

$104k-136k (estimate)

POST DATE

05/28/2024

EXPIRATION DATE

07/26/2024

WEBSITE

conceptlabs.org

HEADQUARTERS

CHICAGO, IL

SIZE

50 - 100

FOUNDED

1995

CEO

JOEL HEIFITZ

REVENUE

$10M - $50M

INDUSTRY

Durable Manufacturing

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If you are interested in becoming a Quality Assurance Supervisor, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Quality Assurance Supervisor for your reference.

Step 1: Understand the job description and responsibilities of an Accountant.

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Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.

Career tips from people on Quality Assurance Supervisor jobs

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