What are the responsibilities and job description for the Quality Associate I (TEMPORARY) position at EKF Diagnostics USA (Stanbio Laboratory)?
Description
TEMPORARY, FULL-TIME Onsite Position
3 months - 6 months
Summary Of Position
The Quality Associate I is responsible for supporting day-to-day quality activities to ensure compliance with the Quality Management System, and procedures therein, and applicable regulatory requirements.
ESSENTIAL FUNCTIONS, Included But Not Limited To
REQUIRED QUALIFICATIONS:
TEMPORARY, FULL-TIME Onsite Position
3 months - 6 months
Summary Of Position
The Quality Associate I is responsible for supporting day-to-day quality activities to ensure compliance with the Quality Management System, and procedures therein, and applicable regulatory requirements.
ESSENTIAL FUNCTIONS, Included But Not Limited To
- Partner with other departments, as needed to maintain product quality, drive and/or support continuous improvement, and ensure accurate and complete documentation.
- Perform batch record review and release activities to ensure all documentation is complete , accurate, and compliant with established procedures and quality standards.
- Perform release activities for materials, components, and finished products, etc.
- Conduct various testing activities, including but not limited to quality control (QC), water testing, Total Organic Carbon (TOC), stability-related activities, and other routine quality testing as assigned.
- Perform environmental monitoring (EM) activities as required.
- Conduct calibration activities for equipment and instruments, including but not limited to weights, thermometers, thermocouples, and other measurement devices.
- Assist with troubleshooting, root cause analysis, and continuous process improvement initiatives to enhance product quality and operational efficiency.
- Support quality system activities related to CAPA (Corrective and Preventive Actions), NCR (Non-Conformance Reports), and planned deviations.
- Provide validation support as needed, including execution and documentation assistance for validation protocols and reports.
- Provide document control support as needed.
- Assist with solution preparation activities as needed, following approved procedures and specification requirements.
- Perform analysis and trending of Quality data as needed to support investigations, process monitoring, and continuous improvement.
- Support internal and external audits, as required.
- Adhere to current Good Manufacturing Practices (cGMP).
- Comply with Company policies, Quality Management System (QMS) and Standard Operation Procedure (SOPs), etc.
- Ensure compliance with safety regulations and procedures are implemented and followed; Maintain clean and safe work area.
- Assist as needed in other areas of the company where training requirements have been completed.
- Perform other duties as assigned.
- None
- None
REQUIRED QUALIFICATIONS:
- Legally authorized to work in the United States.
- High School Diploma or its equivalent.
- Proven quality management systems experience.
- Previous experience of production/manufacturing and quality experience.
- Knowledge of quality system processes such as batch record review, product release, CAPA, deviations, NCRs, document control and validation support.
- Familiarity with statistical process control principles used to monitor and ensure the quality of the production process.
- Ability to perform routine testing and interpret basic quality data.
- Good understanding of laboratory equipment (e.g., pipettes, scales, pH meters).
- Experience using inspection and measurement tools such as calipers, micrometers, multimeters, or similar equipment
- General knowledge of biological and chemical concepts.
- Familiarity with various standards and regulations such as ISO 9001, ISO 13485:2016, the Quality System Regulation (21 CFR Part 820)
- Associate or bachelor’s degree in Biology, Chemistry, Quality, Life Sciences, Engineering, or a related scientific/technical field.
- Experience supporting quality audits, root cause analysis, or corrective actions
- Experience with document control, CAPA, and internal auditing.
- Ability to analyze quality metrics and process data to identify improvement opportunities.
- Direct laboratory experience in a biology, chemistry, or medical environment.
- Experience with performing QC Testing, including assays
- Ability to operate laboratory equipment and understand complex testing protocols including analytical pipetting, enzyme assays, High-Performance Liquid Chromatography (HPLC), and electrophoresis.
- General knowledge of Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) or similar.
- Project a positive company image by interacting with fellow employees, customers, and management in a cooperative, supportive, and courteous manner; displays a professional attitude.
- Detail oriented with a high level of accuracy, efficiency, and accountability.
- Possess a strong commitment to product quality and compliance.
- Excellent organizational skills to meet goals and set priorities.
- Ability to work independently and as a member of various teams and committees.
- Proven ability to handle multiple projects and meet deadlines; work in a fast-paced environment.
- Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm
- Willingness to pivot between lab testing, documentation review, and floor support.
- Ability to operate related office equipment, such as computers, calculator, and copier.
- Able to work with small tools and electronic equipment to test and inspect.
- Demonstrated ability to analyze and interpret information.
- Ability to perform repetitive tasks and use laboratory/manufacturing instruments.
- Working knowledge of Microsoft Excel, Word, and Outlook.
- Able to understand the basic reasoning and process of the scientific method.
- Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form.
- Ability to define problems, collect data, establish facts, and draw valid conclusions.
- Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
- Ability to read and interpret work related documents, procedures, and manuals.
- Ability to communicate effectively; good written and oral communication skills; ability to read, write, speak, and understand the English language.
- Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
- General knowledge of the metric system units (length, area, volume, capacity, mass, and weight) and U.S. equivalents.
- Close visual acuity to perform an activity such as preparing and analyzing data, transcribing, viewing a computer terminal, and reading.
- Ability to work in a laboratory, manufacturing, or controlled environment.
- Must be able to wear and work in personnel protective equipment (PPE) as required.
- Light physical activity performing non-strenuous daily activities in a laboratory setting.
- Ability to hear, understand, and distinguish speech.
- Dexterity and coordination are necessary to handle small components.
- Manual dexterity required for handling samples and performing precise calibrations.
- Frequent repetitive motions that may include the wrists, hands and/or fingers to operate keyboard and mouse.
- Frequently stand for prolonged periods of time.
- Occasionally move about inside the facility to access office machinery, correspond with other departments, attend meetings/training, etc.
- Frequently lift, carry, push, pull or otherwise move objects up to 10 pounds; occasionally carry, push, pull or otherwise move objects up to 25 pounds.
- Occasionally required to climb or balance; squat, stoop, kneel, crouch, or crawl; and smell.
- Occasionally reaching for items above and below desk level.
- The ability to hear, understand, and distinguish speech.
- Frequently communicate information and ideas with others to exchange information and understanding. Able to exchange accurate information in these situations.
- Well lit, heated/air-conditioned indoor laboratory setting with adequate ventilation.
- The noise level in the work environment is moderate.
- Frequent exposure to low temperatures in controlled refrigerators and/or freezers.
- Occasional exposure to biohazards, fumes and other airborne particles.