Director of Quality Operations (m/f/d)
Your Strength
- 10+ years of experience in quality management in a manufacturing organization within the medical industry
- Focus of experience on Quality Operations/Manufacturing
- Extensive knowledge of FDA regulations, ISO 13485, and other relevant quality standards
- Proven leadership experience in quality control, manufacturing quality, and process validation
- Strong analytical, problem-solving, and decision-making abilities
- Excellent communication, interpersonal, and team leadership skills
- Experience in managing audits, regulatory inspections, and compliance initiatives in the Operations-Field.
- Pragmatic, but compliant approach.
Your Contribution
- Oversee manufacturing control, quality control, and quality control laboratory operations to ensure compliance with FDA, ISO, and other applicable regulations
- Release of products to the markets
- Lead qualification of equipment, verification and validation of processes, and change control activities
- Ensure robust product lifecycle management
- Establish and monitor key performance indicators
- Lead change control for sustaining business
- Develop and mentor the sustain quality team, fostering a culture of quality awareness and operational excellence
- Collaborate cross-functionally
- Serve as the primary point of contact for quality-related communications with internal stakeholders, regulatory authorities, and external customers
Our Strength
- An exciting field of activity in a global team
- An independent area of responsibility
- Intensive training with mentoring program
- Various benefits such as hybrid working, business bike, company pension and subsidy for our canteen
Contact
Apply now and join the Artivion team. We look forward to hearing from you!
Maximiljane Tyrs, jobs.europe@artivion.com, T: 07471 922 352
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,
Lotzenäcker 23, 72379 Hechingen
www.artivion.com
