Quality Specialist Healthcare Manufacturer Base Salary to 80kyear Los Angeles CA

AllSearch Professional Staffing; Los Angeles (CA); On-site; USD 80,000; Full time

Job summary

Ein führendes Unternehmen in der Herstellung von medizinischen Kunststofffolien sucht einen Quality Specialist, um das Team zu verstärken. In dieser Rolle sind Sie für die Initiierung neuer Spezifikationsnummern verantwortlich und verwalten Dokumentenänderungen im ERP-System. Sie arbeiten eng mit den Verkaufs- und Operationsteams zusammen, um sicherzustellen, dass Kundenanforderungen präzise in interne Dokumente umgesetzt werden. Wenn Sie eine Leidenschaft für Qualitätssicherung haben und in einem dynamischen Umfeld arbeiten möchten, ist dies die ideale Gelegenheit für Sie.

Qualifications

• Mindestens 2 Jahre Erfahrung in der Qualitätssicherung in regulierten Branchen.
• Starker Hintergrund in der Dokumentation von Qualitätsprozessen.

Responsibilities

• Verantwortlich für den gesamten Spezifikationsprozess neuer Aufträge.
• Identifizierung von Qualitätsproblemen in Dokumentenstruktur und Änderungsmanagement.

Skills

Qualitätskontrolle

Dokumentationsmanagement

Kommunikation

Problembehandlung

Education

Associate Degree

Bachelor of Science Degree

Tools

QAD ERP System

EQMS Systeme

Vision Systeme

Job description

Quality Specialist - Healthcare Manufacturer - Base Salary up to $80k/year - Los Angeles, CA

Our client, a leading manufacturer of plastic films used in the healthcare and medical device manufacturing industries, is seeking a Quality Specialist to join their team.

The Quality Specialist will initiate new master and item specification numbers for all incoming drawings and specifications, transferring this information into the company's specification process. The role also involves managing all document control changes and creating or editing items in the ERP system to facilitate easy access to specifications for Sales and Operations teams.

Responsibilities:

1. Act as the 'input' owner for all aspects related to the specification process for new orders.
2. Identify quality issues related to document structure, format, and change control.
3. Update QAD system as needed for changes in specifications, bill of materials, wind-ups, and blender sheets.
4. Serve as a liaison between Sales/Marketing and Operations to ensure customer specifications are accurately converted into internal documents for easy reading.
5. Manage weekly specification meetings.

Qualifications:

1. Associate Degree or Bachelor of Science Degree.
2. At least 2 years of experience in quality within a regulated industry.
3. Strong background in documentation related to quality processes.
4. Experience with regulated industries such as ISO or FDA.
5. Familiarity with ERP and EQMS systems, preferably QAD.
6. Ability to operate and manipulate Vision Systems by reviewing output data.

Compensation:

The role offers a base salary of up to $80,000 per year along with a comprehensive benefits package.