Quality Systems Specialist job at Medical Devices Company. Louisville, CO.
Roles & Responsibilities
PRIMARY RESPONSIBILITIES AND DUTIES include the following.
- Responsible for Quality Systems activities as assigned.
- Follows applicable corporate quality procedures and makes updates to procedures, policies, training matrices and curriculums.
- The Quality Systems Specialist will be accountable for basic application of Quality Systems principles in the areas of document control and other broad quality systems areas.
- Prepare, create and maintain various types of documents such as quality documents and manufacturing specifications for BD products and services.
- Assist in the development and evaluation of new processes and procedures.
- Analyze existing processes and procedures to suggest continual improvements.
- Provide general audit support.
- Other duties and responsibilities as assigned.
- Performs day-to-day activities under direct supervision
- Follows specific, detailed instructions
- Notifies manager upon recognition of factors that may affect project deliverables
Experience Required
EXPERIENCE
0 - 2 years experienceSkills & Certifications
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.The requirements listed are representative of the knowledge, skill and / or ability required.Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.Excellent communication, problem-solving, organizational and interpersonal skillsComputer skills (Excel, Word, Power Point, etc.)Self-motivated and directed, requiring minimal supervisionDemonstrated ability to work in teams to obtain results is required.Effective skills in analytical thinking and problem-solving required.Eligibilities & qualifications
EDUCATION
Bachelors Degree in Quality Engineering or related Science discipline preferredJ-18808-Ljbffr