Avery Dennison
Medical Device
QualityControlManager
Neural analysis suggests this role is
optimal for mid candidates.
“Quality Control Manager at Avery Dennison. Skills: Quality management, Regulatory affairs. Manage quality function. Provide work direction for quality engineers and inspectors”
Industry & Context.
What They're Looking For.
Must Have
Bachelor’s degree in Engineering or scientific field, 4 years experience in medical device or pharmaceutical industry, 3 years experience in regulatory compliance and quality systems, 4 years experience in managing a team
What You'll Do.
Manage quality function
Provide work direction for quality engineers and inspectors
Establish quality standards for raw materials
Formulate strategy to foster high-performance culture
Coach and develop staff supporting quality function
Drive improvements to the quality system
Ensure compliance with cGMP
Work closely with commercial and operations to build
Engage with customer quality representatives
Implement innovation and improvement plans
How You'll Work.
Team & Collaboration
Interact with engineering, manufacturing, and service functions; Work with commercial and operations; Engage with customer quality representatives
Communication Scope
Written communication; Verbal communication; Presentation skills
Full Job Description
About the role You will manage the quality function by providing work direction for quality engineers and inspectors and interact regularly with engineering, manufacturing, and service functions to establish quality standards for raw materials, work in process, and finished products. Key Responsibilities This position operates on an on-site / hybrid work schedule (role-dependent). * Formulate a strategy to foster a high-performance culture with quality right first time suitable for a world-class medical device contract and legal manufacturer. * Coach and develop staff who support the quality function during the manufacturing process and drive a culture of quality awareness. * Drive improvements to the quality system that ensures its suitability, adequacy, and effectiveness. * Understand and ensure compliance with cGMP, ISO 13485, and FDA 21 CFR Part 820 regulations. * Work closely with commercial and operations to build value with top 10 key accounts and engage with customer quality representatives directly to implement short, medium, and long-term innovation and improvement plans. ## Qualifications Required: * Bachelor’s degree in Engineering or a scientific related field. * A minimum of 4 years of experience in the medical device or pharmaceutical industry with at least 3 years of experience in regulatory compliance and quality systems. * At least 4 years of experience in managing a team. Skills you need to succeed: * Thorough knowledge of ISO 13485 and 21CFR Part 820. * Strong written and verbal communication skills alongside strong presentation skills, with the ability to effectively work with various functions and levels within the organization. ## Additional Information What we offer * Financial & Health Benefits: Includes Healthcare allowance, Insurance & Pension (for salaried employees), Service Awards, and Gift Vouchers for celebrations. * Time Off & Flexibility: Enjoy additional leave based on seniority (up to 25 after 10 years), and flexible working arran
Applying for this Quality Control Manager role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on SmartRecruiters
- SmartRecruiters often includes a video screening step — check camera and mic permissions.
- Link your GitHub or portfolio directly in the profile section for technical roles.
- Applications may be reviewed by AI scoring before reaching a recruiter — use keywords from the job description.
ANONYMOUS · UNFILTERED
What do employees actually say about Avery Dennison?
Real rants from real employees. Read before you apply.