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MK
Mary Kay
Specialist Quality Systems
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What they do
A Quality Assurance Auditor regularly evaluates the quality control systems in place and verifies compliance with quality and safety standards.
$54,429 / year median in Texas
-1% projected decline
Job Description
Specialist Quality Systems ๐ Lewisville, Texas - R3 MFG/R D New ๐ Quality Assurance ๐
๎ค ๎ธ ๎ 11 hours ago Post Date ๐
๎ค ๎ธ ๎ 54 Total Views Apply for Job Share this Job Sign Up for Job Alerts Job Summary Serves as technical/subject matter expert for compliance quality related issues and works to resolve these issues and improve quality globally. Serves as internal auditor and member of Quality Systems team. Assists in the day-to-day operations of Quality Systems processes including but not limited to Batch Record Review, Over the Counter (OTC) Drug and Nutritional Product Release, Annual Product Review (APR), Validation Support, Change Control, Training, Document Control, Document Distribution, Investigation and Root Cause Analysis, and Inspection Readiness.
- Quality Management System (QMS) - responsible for duties relating to Quality Systems including but not limited to batch record review, document control, change control, annual OTC product review, validation support, stability support, review of quality events, and investigation of market quality events.
- Inspection Readiness - Must remain knowledgeable about significant global regulatory changes that could impact Mary Kay products.
- Root Cause Analysis - Performs and advises on root cause analysis for product quality issues and works issue through containment phase of corrective action process.
- Internal Auditor - serves as internal auditor ensures that the site is operating in state of compliance.
- This job requires on-site work at a Mary Kay facility.
Experience:
3+ years quality assurance or quality controlEducation:
Bachelor/University Degree, Chemistry, Microbiology Additional Skills & Abilities- Must have a good understanding of advanced quality principles, of audit protocol, inspection procedures and FDA and cGMP regulations. Must be familiar with compliance requirements for over the counter (OTC) products. A knowledge and understanding of multiple manufacturing processes/formulations, international requirements and bilingual skills are beneficial.
- Ability to apply advanced principles, theories, and concepts and contribute to the development of new principles, systems and concepts.
- Must be a critical thinker and active listener with good time management ability to provide solutions and define deliverables to a wide range of difficult and complex problems which require the regular use of ingenuity and creativity. Solutions should be imaginative, thorough, and practicable.
- Must have sound and comprehensive oral and written communication skills to interact with various levels of personnel from different cultures both within and outside the company.
- Must be able to perform duties under very general direction and independently perform assignments with only general criteria for expected results.