What are the responsibilities and job description for the QA Associate position at DiaSorin?
- Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world.
- Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry.
Job Scope
Participating in the design, creation, and implementation and monitoring of programs and methodologies to ensure that Luminex products meet established specifications, design criteria, quality standards and customer requirements. Sharing responsibility for Quality Assurance operations associated with Luminex products and processes. Thorough knowledge of the Diasorin Quality Management System is essential to competently fulfill the duties of the position.
Key Responsibilities and Duties
- Review and approve manufacturing records (includes all manufacturing department BPRs) and QC Records (department tests and inspections)
- Review and approve Device History Records
- Release products for distribution.
- Review Product Lot Request records
- Review and approve pilot lots
- Participate in performing CAPA effectiveness checks, CAPA follow-up and ANR follow-up
- Review and approve ECOs and DCOs as assigned
- Log, file, maintain and archive various QA records
- Prepare materials for QA meetings and, as assigned, present materials at QA meetings.
- Coordinate resolution of quality issues with internal personnel and departments
- Participate in audits and inspections
- Support and participate in other QA related activities as required.
- Other duties as assigned.
QUALIFICATIONS
- Associate degree in a life science or engineering or equivalent related experience
- 3 years' of experience in Quality Assurance activities
- 1 years' of experience with participating in formal audits
- 1 years' of experience in Medical Device Manufacturing environment
- 1 years' knowledge of cGMP regulations (21 CFR 820, CMDR and ISO 13485)
- Detail oriented
- Competency in use of Microsoft Excel, Word and Outlook
- Excellent interpersonal, communication and organizational skills.
What we offer/Salary Range |
We are an equal opportunity employer that values diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply.
This contractor and subcontractor shall abide by the requirements of 41 CFR 60-1.4(a), 41 CFR 60-300.5(a) and 41 CFR 60-741.5(a). These regulations prohibit discrimination against qualified individuals based on their status as protected veterans or individuals with disabilities, and prohibit discrimination against all individuals based on their race, color, religion, sex, sexual orientation, gender identity or national origin. Moreover, these regulations require that covered prime contractors and subcontractors take affirmative action to employ and advance in employment individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.
DiaSorin Inc and DiaSorin Molecular LLC are Affirmative Action and Equal Opportunity Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Salary : $23 - $33