Quality Documentation Control Specialist (maternity cover) at Avery Dennison
Longford, County Longford, Ireland -
Full Time


Start Date

Immediate

Expiry Date

15 Nov, 25

Salary

0.0

Posted On

16 Aug, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Communication Skills, Interpersonal Skills, Documentation

Industry

Pharmaceuticals

Description

COMPANY DESCRIPTION

Avery Dennison Corporation (NYSE: AVY) is a global materials science and digital identification solutions company. We are Making Possible™ products and solutions that help advance the industries we serve, providing branding and information solutions that optimize labor and supply chain efficiency, reduce waste, advance sustainability, circularity and transparency, and better connect brands and consumers. We design and develop labeling and functional materials, radio frequency identification (RFID) inlays and tags, software applications that connect the physical and digital, and offerings that enhance branded packaging and carry or display information that improves the customer experience. Serving industries worldwide — including home and personal care, apparel, general retail, e-commerce, logistics, food and grocery, pharmaceuticals and automotive — we employ approximately 35,000 employees in more than 50 countries. Our reported sales in 2024 were $8.8 billion. Learn more at www.averydennison.com.

JOB DESCRIPTION

The Quality Documentation Control Specialist will maintain procedures related to the document control activities within quality systems to ensure compliance with: - cGMP, FDA 21 CFR Part 820, MDR and ISO 13485 requirements.

QUALIFICATIONS

  • 3rd level qualification in a scientific or technical discipline desirable or work experience equivalent;
  • At least 3 years’ experience in Quality Assurance/Quality Systems and Documentation or equivalent;
  • Good interpersonal skills and acts with integrity;
  • Computer literate (Microsoft Office suite, Doc Control, ERP working knowledge).
  • Rigorous attention to detail.
  • Strong organizational and communication skills.
  • Quality Systems Audits and documentation experience preferred
  • cGMP environment experience preferred.

How To Apply:

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Responsibilities

Please refer the Job description for details

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