Quality Control Specialist

Revvity•Greenville, NC

12h•$55,000 - $70,000•Onsite

About The Position

Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000+ colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health. Find your future at Revvity

Requirements

BS/BA Degree in a scientific/technical field and 2+ years working in a regulated environment.
OR AS Degree in a scientific/technical field and 4+ years working in a regulated environment.
Proficient skills with Microsoft Office (Word, Excel, PowerPoint)
Strong organization skills required.

Nice To Haves

ASQ Certifications a plus.
Working with Pharma or Medical Devices preferred
Experience with ISO 13485 or ISO9001 preferred.
Demonstrated ability to work effectively and positively with all levels of an organization.
Capable of working both independently and in a team setting; team oriented and committed to continuous improvement.

Responsibilities

Responsible for Document Control and Records Retention.
Trends data from Quality System inputs and creates monthly charts and reports.
Assists in Quality Management Review preparation.
Assists with Failure Investigations (Complaint, Non-Conformance, Supplier, etc.)
Participates in internal audit program.
Works with Quality and Operations management on short and long term quality planning and quality system improvements initiatives.
Drafting new, and revising existing Standard Operating Procedures (SOP)
Approval to ship conforming product following full review of process documentation.
Make records of quality activities per specified procedures.
Maintain all required documentation of work performed and ensure that all forms and materials are labeled properly.