Senior Quality Assurance Technician Jobs in Union, Arkansas

Working knowledge of test management software (e.g. TestFLO for Jira)

Excellent verbal and written communication skills

1+ year of Quality Assurance testing experience

Experience with Point-of-Sale software applications

We provide a collaborative environment and encourage knowledge sharing.

· Create detailed test cases for full system requirement coverage/traceability

Experience with DevOps processes, typically using an Agile methodology

Experience in monitoring and interpreting real-time Application Insights results

Previous experience with Azure and Microsoft technologies that relate to QA, including Azure DevOps.

Experience with automated, manual, integration and end-to-end/system testing is required.

Strong knowledge of software quality assurance principles, methodologies, and processes.

Develop and implement a strategic and comprehensive QA program.

G. Three years of experience with Application Lifecycle Management, tracking bug fixes, test results, and release management.

*Candidates chosen for an interview will meet the Education, General Experience and Specialized Experience requirements.

A. Two years of experience with establishing and executing automated test procedures.

B. Three years of software testing experience (integration and acceptance) on multiple projects.

D. Three years of experience testing database interfaces in a multi release project environment.

A. Determine the resources required for quality control.

Escalates issues with late SCARS to Quality management through email notifications and/or monthly metrics.

Supports in maintaining current versions of departmental and factory documents, including 3rd party audit certifications, ingredients and supplier approval documentation.

Issues, monitors, and manages SCAR system for raw material supplier non-conformities.

Successfully completes projects (with approval from supervisor/manager) in a timely manner with minimal supervision.

Outstanding written and verbal communication skills

Strong background and intimate knowledge of manufacturing as it relates to soda CSD manufacturing.

Mastery knowledge and expert experience with system development, data analysis, analytic application, reporting, administrative data sources, data use policies and procedures.

Mastery skills in analyzing healthcare service requirements and formulating policies. Ability to plan, organize, and implement independent projects concurrently.

Mastery knowledge of Quality Framework for long-term care programs.

Works with healthcare provider organizations and healthcare advocacy organizations on policy and programmatic changes.

Provides training and support to the Quality Improvement Strategy team on systems, policies, and procedures.

to support a local contract.

• 2+ years of people management experience (required).

• 5+ years of experience working with quality management system (desired).

The Senior Quality Assurance Manager will:

• Bachelors Degree with relevant fields with 4+ years of medical device industry experience.

• A competitive salary and stock option plan along with a range of benefits

• opportunities for continuing education.

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Works under FSQA management guidance to ensure compliance with Foster Farms, FSIS/USDA, and customer requirements.

Ensure food safety documentation meets legal/regulatory requirements.

Good organization skills and legible handwriting.

Must have good interpersonal skills and communication skills.

Must be willing to rotate into various departments with varying QC related job duties as needed.

Ensure compliance to Food Safety systems through monitoring of process and documentation.

Providing accurate and timely information to department managers

Must obtain lab certification by state and/or FDA

Must have analytical and problem solving skills

Must have good human relations skills (the ability to work well with others and be a team player)

Must possess basic math skills

providing accurate and timely information to department managers

Minimum of 5 years of experience in quality management

Prior experience in a quality management system within a manufacturing environment. Preferably ISO9001 and ISO13485

Ensures all sites meet quality management standards of ISO9001 and ISO13485. Manage site audits.

Must be able to work on multiple projects simultaneously and demonstrate organizational, prioritization, and time management proficiencies.

Prior experience in support internal and external audits

Knowledge of robotic liquid handling or comparable complex scientific lab equipment

Interact with plant and QA management for communication of any and all problems

All other duties assigned by manager

2+ years’ experience working in food quality, lab, manufacturing, production, or related environment.

Proficient in basic computer skills such as Microsoft Office applications

Strong communication skills and organization skills

proficient in basic computer skills such as Microsoft Office applications

Excellent problem-solving skills and experience with root cause investigations and CAPA determination

Knowledge of U.S. and international regulatory standards and guidelines

Strong computer skills including MS Office (Word, Excel)

Experience with rare diseases, neuromuscular diseases and/or gene therapy products

Experience in a small company and high growth, fast-paced environment

Perform review and approval of master production batch records.

Complete the Post install Quality Control Scorecard and submit it to the Installation Manager weekly.

Facilitate training under the guidance of the Installation Manager to address opportunities, prevent further recalls and minimize customer concerns.

Handle customer concerns in a proactive and timely manner resulting in a positive experience for the customer.

Develop quarterly training schedule in collaboration with the Installation Manager.

Are you detail-oriented with a desire to be respected for your knowledge?

Installation Recalls and Zero Calls:

Monitors all HACCP requirements and regulations from raw material receiving through the raw room

Bachelor of Science Degree in Food Science, Biology, Chemistry, or related field, OR experience in the quality assurance field

Some food industry knowledge: meat industry is a plus

Monitors quality control of raw materials and oversee the activities in the raw room and storage areas related to quality assurance

Conduct investigations for customer complaints and report findings

Work on special projects as assigned

Must have knowledge of proper procedures for handling chemicals and laboratory safety procedures;

Have knowledge of proper procedures for handling chemicals and laboratory safety procedures.

Have adequate knowledge of safe lifting procedures, “lockout/tagout” procedures, and proper safety procedures.

Communication skills and the ability to work well with others and U.S.D.A Inspectors are a must.

Inspect and analyze meat raw materials and finished products using physical (organoleptic), chemical and microbiological methods;

Monitor incoming and outgoing shipments of product;

REQUIRED EDUCATION, EXPERIENCE & SKILLS:

PREFERRED EDUCATION, EXPERIENCE & SKILLS:

Assist quality manager / metallurgical engineer in material evaluation, trials, and product recipes.

Engineering experience and a strong understanding of foundry processes, materials, and equipment

Basic computer skills with advanced proficiency in Excel for data analytics

Strong analytical skills and possess the ability to enforce company policy and make good decisions independently

1-3 years prior production/manufacturing experience or 2+ years relevant lab technician experience.

Food/beverage industry experience a plus.

Good computer skills including literacy with Excel and Word.

Blending experience is a must.

Food/beverage industry experience a plus

Total Wellness Programs including health, dental and vision plans

Uses complete understanding and wide application of technical concepts, standards,and practices in chosen field and is expanding knowledge or related disciplines

Full knowledge of industry standards and Good Lab Practices

Applies analytical skills and independent judgment to develop innovative, practical, and consistent solutions to a wide range of complex problems

Working knowledge of U.S. and international regulations (QSR, ISO, GLP, cGMP)

Experience working under pressure, prioritizing, and multitasking quality issues in real-time

Excellent oral and written communication skills

Experience with us of ethylene oxide and at least one additional sterilization modality (e.g. radiation, moist heat, dry heat)

Good interpersonal and organizational skills.

Experience with GMP audits, internal and relevant external audits

Experience with overseeing biocompatibility studies

Work directly with the BWI R&D teams to validated and transfer break-through technologies to enable future growth and innovations.

Drive selection of sterilization modality, validation approaches and validation of the sterilization process for new products, and the sites for execution.