Quality Systems Specialist
Vonco Products LLC
Job Description
Job Description
Description:
Basic Purpose and Function:
Independently perform quality-related functions within the Quality Department. Maintain and monitor quality systems, including document control, change control, CAPA (Corrective and Preventive Actions), internal audits, and complaint handling.
Job Responsibilities:
· Manages the review cycle of customer complaints and CAPA’s
· Lead internal audit program
· Assist in the development, revision, and control of Standard Operating Procedures (SOPs) and other controlled documents.
· Identify training needs and conduct Quality Assurance-related training to associates in tandem with the Quality Manager
· Facilitate the nonconformance process and ensure timely investigation, root cause analysis, and resolution.
· Supports the maintenance and upkeep of the Quality Management System
· Support performance metrics system for continual improvement
· Assist with inspections, document reviews, and data entry when additional support is required to maintain production or quality timelines.
We offer flexible working hours to support business needs and work-life balance. Specific schedules will be discussed during the interview process.
Other Responsibilities:
· Responsible for adhering to the quality system and good manufacturing procedures
· Must be able to communicate effectively with the supervisor and co-workers to provide and receive directions
· Demonstrate good time management skills independent of supervision
· Maintain timely and regular attendance per company policy
· Performs other duties as assigned
Requirements:Qualifications:
· Associates degree or equivalent; or 3-5 years related experience and or training; or equivalent combination of education and experience in medical device manufacturing
· Proficient in applicable regulations/standards (ISO 13485, FDA, etc.)
· Ability to read, analyze, and interpret general business periodicals, professional journals, or governmental regulations.
· Ability to write reports, business correspondence, and procedure manuals
· Ability to effectively present information and respond to questions from employees, supervisors, managers, executive staff, customers, and suppliers
· Reaching, standing, walking, pushing, pulling, lifting, typing, grasping, feeling, talking, hearing, seeing and repetitive motions
· Proficiency in Microsoft Word, Excel, and Outlook or similar e-mail programs
· Responsible for adhering to the quality system and good manufacturing procedures
· Must be able to communicate effectively with the manager and co-workers to provide and receive direction
· Demonstrate good time management skills independent of supervision
· Maintain timely and regular attendance per company policy
Other: Spanish language and bilingual skills a strong plus
Physical Requirements:
· Reaching, standing, walking, pushing, pulling, lifting, typing, grasping, feeling, talking, hearing, seeing and repetitive motions
· The associate must occasionally lift and/or move up to 40 pounds
· Specific vision abilities required by this job include close vision and the ability to adjust focus
$96k - $132k
...by work that is never the same from one day to the next. As a Quality Associate III, you are unafraid of navigating through necessary... ...individual contributor ownership and oversight of Quality Management System processes including change control, CAPA, complaints,...SuggestedOdd jobTemporary workWork at officeWorldwideWork visaFlexible hours$96k - $132k
...exceptional results. Here, you will find more than just a job—you will find purpose and pride. Your role at Baxter The Quality Associate III (Quality Engineer) is a key individual contributor responsible for driving quality engineering initiatives and...SuggestedTemporary workWork visaFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Quality Systems Specialist. Be the first to apply!
