Quality Coordinator Job at Alro (Louisville)

Quality Coordinator

We are looking for a Quality Coordinator to join a manufacturing team on a contr...

Location

United States , New Berlin

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Minimum of 2 years of experience in quality assurance, quality coordination, or a related role within manufacturing or food production
Working knowledge of quality systems, documentation practices, and food safety or sanitation compliance requirements
Ability to investigate issues, organize findings, and contribute to practical corrective action plans
Experience delivering training or coaching employees on procedures, standards, and compliance expectations
Strong communication skills with the ability to work effectively across quality, production, and other cross-functional teams
Comfortable spending time in a production environment and identifying conditions that may affect product quality or safety
Proficiency in reviewing records, maintaining accurate documentation, and analyzing quality data to support decision-making

Job Responsibility

Monitor quality and sanitation records to confirm compliance with food safety and internal standards, and follow up on any gaps that require correction
Support investigations into customer concerns, internal holds, and process-related quality issues while helping drive corrective and preventive actions
Train new and existing employees on food safety practices, quality procedures, work instructions, and standard operating methods
Partner with production and support teams to improve processes, address nonconforming conditions, and promote continuous improvement across operations
Observe activity on the production floor, reinforce safe and compliant behaviors, and escalate concerns related to quality, food safety, or sanitation
Track findings from hygiene and fabrication inspections and help ensure timely completion of corrective actions
Assist with verification and validation activities for preventive controls under the direction of quality leadership
Review quality-related data to identify trends, highlight problem areas, and support improvements in manufacturing methods
Provide backup support for quality technician responsibilities and complete additional quality tasks as assigned by management

What we offer

medical
vision
dental
life and disability insurance
401(k) plan

Quality Coordinator

The Quality Coordinator ensures that products manufactured meet internal quality...

Location

United States , Northlake

Salary:

70000.00 - 80000.00 USD / Year

SIG Group

Expiration Date

Until further notice

Requirements

Minimum of 3 years required
or equivalent combination of education and experience in Quality or Continuous Improvement
Fluent in English (written and verbal)
MS Office (Intermediate)
Strong background in applying tools like Process FMEA and Quality Control Plans to proactively identify risks, reduce failures, and improve manufacturing processes
Proficiency in Statistical Process Control (SPC), control charts, and quality monitoring tools to analyze process performance and drive data-based decisions
Experience managing internal and customer complaints using structured problem-solving (SPS) methodologies and conducting thorough root cause analysis to implement corrective actions
Ability to support and implement quality skill matrices, train teams on critical procedures, and promote a strong culture of quality and continuous improvement on the plant floor
Skilled in maintaining accurate quality documentation, including inspection reports, non-conformance logs, Certificates of Conformance (CoC), and managing retained samples with full traceability

Job Responsibility

Ensure that the required Standard Operating Conditions (SOC) / process parameters linked to the product/equipment compliance is actively monitored and managed
Support the use of the Quality skill matrix at the operational level, ensuring adequate training regarding critical quality procedures
Support changes of global valid manufacturing and process specifications in the production process
Ensure the avoidance / reduction of the occurrence of potential failures through the systematic and comprehensible application and use of the Process FMEA and Quality Control Plan
Manage and control internal complaints based on a structured problem solving (SPS) process
Ensure compliance with quality and food safety management systems
Assist with statistical process control (SPC), control charts, and other quality monitoring tools
Support root cause analysis related to customer complaints
Promote a culture of quality and continuous improvement on the shop floor
Maintain accurate quality records, inspection reports, non-conformance logs, and corrective action documentation

What we offer

Generous Day 1 eligibility healthcare & life insurance for you and qualified dependents
401K Retirement matching reimbursement
Vacation & PSL
Paid Holidays
Performance Bonus
And much more!

Fulltime

Quality Coordinator

The Quality Coordinator assists with coordinating quality activities of a design...

Location

United States , Rockford

Salary:

18.15 - 20.42 USD / Hour

PCI Pharma Services

Expiration Date

Until further notice

Requirements

TABE testing requirements met at approved grade level for position
Basic Mathematical Skills
Intermediate Computer Skills: Ability to perform more complex computer tasks and has knowledge of various computer programs
Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs
Very High Reasoning: Ability to define problems, collect data, establish facts, and draw valid conclusions
Be able to interpret an extensive variety of technical instructions in math or diagram form and deal with several abstract/concrete variables
High School Diploma or GED
2 years of experience in Operations/Quality and/or providing support in an office or manufacturing environment

Job Responsibility

Prepares and distributes required documentation for requested production work orders
Perform documentation and records review of completed orders to ensure compliance with cGMP's and customer requirements
Creating and updating batch records, forms and material specifications as well as organizing internal and customer approval of batch records and specifications
Performs and submits batch records, accountability reports and necessary documentation to customers to facilitate product release
Help identify, communicate, track and resolve document related issues with other departments and customers
Function as one of the customer points for comments or questions pertaining to batch documentation
Assist with providing quality related metrics
Performs finished product batch release of approved production lots
Meet with management to address issues or concerns with the batch documentation
Reviews and interprets customer standards, procedures and specifications for dissemination relative to batch records, forms and material specifications. Organize internal and customer approval of batch records and specifications

What we offer

paid time off
health insurance coverage (including dental and vision)
flexible spending account
401(k)
eligibility for an annual performance bonus

Fulltime

Quality Coordinator

This is a fantastic opportunity for an experienced Quality Assurance professiona...

Location

United Kingdom , Bridgwater

Salary:

40000.00 - 45000.00 GBP / Year

Hunter Selection | B Corp™

Expiration Date

Until further notice

Requirements

Previous experience working within the quality department for a manufacturing company
Strong working knowledge of ISO 9001, ISO 14001, and AS9100
Experience working with automotive and aerospace customers
Ability to interpret engineering drawings
Ability to manage quality systems

Job Responsibility

Support Continuous Improvement initiatives across the team
Manage the Quality Assurance processes
Oversee internal and external audits – working closely with the assigned consultant
Manage all customer complaints and non conformances
Responsible for monitoring internal quality KPI’s
Perform and manage inspection, calibration and FAIR activities
Ensure compliance with relevant standards

What we offer

Bonus
31 days holiday
Onsite parking
Pension

Fulltime

Quality Coordinator

As a Quality Coordinator, you will play a key role in ensuring that every guest ...

Location

Spain , Tenerife

Salary:

Not provided

Marriott Bonvoy

Expiration Date

Until further notice

Requirements

Strong attention to detail, analytical thinking, and a passion for excellence
Previous experience in Quality, Guest Experience, Front Office, or operational roles within luxury hospitality or high-standard environments
Ability to work cross-functionally with multiple departments and levels of the organization
Strong communication, influence, and follow-up skills
Proactive, organized, and results-oriented mindset
Fluency in English and Spanish
Valid work permit for Spain

Job Responsibility

Ensuring the correct implementation and compliance with The Ritz-Carlton Gold Standards across all areas of the resort
Coordinating and following up on internal and external quality audits, as well as action plans derived from them
Analyzing guest feedback (GSS, Qualtrics, internal and external surveys) to identify opportunities for continuous improvement
Leading quality and operational excellence initiatives in collaboration with all departments
Monitoring and following up on guest incidents and complaints, ensuring resolutions aligned with brand standards
Preparing quality reports, KPIs, and performance summaries for senior leadership
Supporting ongoing training of teams in service standards, quality culture, and guest experience
Ensuring proper documentation and updates of quality-related standard operating procedures
Actively participating in special projects focused on innovation, service consistency, and guest satisfaction

What we offer

Competitive salary above market and flexible compensation
Explore Rate benefits at more than 9,500 Marriott hotels worldwide, extended to family members, partners, and parents
20% discount on Food & Beverage across all our hotels and 50% discount on the resort’s own culinary offerings
Up to 75% discount on flights for Tenerife residents to mainland Spain
Corporate benefits with multiple leisure and travel discounts
Special birthday gift
Complimentary guest stay at our resort after one year of service
13th and 14th salary payments
Continuous training through our corporate university
Career development and growth opportunities within an international company

Fulltime

Quality Coordinator

The key purpose this role is to lead and conduct clinical audits, with the aim o...

Location

Ireland

Salary:

Not provided

Blackrock Health Hermitage Clinic

Expiration Date

Until further notice

Requirements

Clinical background is essential
Qualification in auditing is desirable
Experience with IT / administration systems
Experience in a Quality/ Healthcare environment desirable
Experience working on own initiative and with multidisciplinary stakeholders
It is essential that you have valid work permission for the Republic of Ireland to take up employment for this position, or in the case of critical skills, you must be eligible for a work permit.

Job Responsibility

To conduct clinical audits including but not limited to reviewing charts, other documentation, and observation of practice
Liaise with the Quality and Risk Manager to set up audit schedules and review current audit frameworks
To facilitate clinical audit work across the organisation
Provide advice guidance and support to staff undertaking clinical audit projects
Ensuring that audits comply with the principles of good practice
To work closely with hospital departments in conjunction with the Quality team to provide reports and feedback on audits conducted
Develop an audit and monitor compliance
Validate auditors in line with hospital policy and JCI /HIQA requirements
Review patient records or other data sources and accurately and completely record information in accordance with the audit design and protocols
Maintain strict confidentiality in relation to patient identifiable information

What we offer

Competitive salary
Pension
Discounted café
Sports and Social club
Employee Assistance Programme
Discounted onsite pharmacy

Fulltime

Office Coordinator - Quality Management

Responsible for clerical and secretarial duties, scheduling, and coordinating ca...

Location

United States , Beaumont

Salary:

Not provided

CHRISTUS Health

Expiration Date

Until further notice

Requirements

High school diploma or equivalent
One (1) year related experience required

Job Responsibility

Responsible for assisting staff in all aspects of departmental management
Coordinates internal activities of department
Displays telephone courtesy and relays messages accurately
Maintains policy and procedure manuals, job descriptions, Standards of Care/Practice, and Nursing protocol
Prepares and distributes and files reports, correspondence, documents, minutes, and memorandums
Performs receptionist duties, greets all persons, answers questions
Performs other tasks as delegated by Director, such as maintaining daily activity calendar and making travel arrangements
Reserves conference room
Complies with timekeeping system
Attends department staff meetings

Fulltime

Coordinator Quality Management

In a High-Reliability Organization, the QM Coordinator, reporting to the Directo...

Location

United States , Santa Fe

Salary:

Not provided

CHRISTUS Health

Expiration Date

Until further notice

Requirements

Graduate of an accredited nursing school or practical certificate program is required
Three years of healthcare experience
LVN/LPN or RN license required

Job Responsibility

Meets expectations of the applicable OneCHRISTUS Competencies: Leader of Self, Leader of Others, or Leader of Leaders
Communicate effectively to different audiences
Proficient in computer skills using EXCEL, PowerPoint, MS Office, and Flowchart tools
Knowledgeable of High-Reliability Principles and PDSA methodology

Fulltime

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Quality Coordinator

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