AdresQuality Assurance Specialist - 2406176568W
Description
About Johnson & Johnson
_At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/._
JOB SUMMARY
Entry level to developing individual contributor, who works under close supervision. Contributes to the processes and activities related to fulfilling the Quality Assurance requirements for the organization's products. Develops close partnerships with customers and key stakeholders. Uses data to identify risks and improvement opportunities. Implements risk mitigations and process improvements with support. Escalates issues and risks as required.
DUTIES & RESPONSIBILITIES
o Applies functional knowledge of Quality Assurance requirements to support organizational objectives.
o Assists with review of documentation associated with processes and activities related to the organization's products.
o Assists with routine data collection, analysis, and reporting to ensure the continuous improvement of the quality management system.
o Leads implementation of risk mitigations and continuous improvement projects under supervision.
o Carries out processes to ensure the internal organization's alignment with overall quality priorities under direct supervision.
o Follows formal escalation processes to ensure visibility of risks associated with product quality, regulatory compliance, and quality systems.
o Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
Qualifications
EXPERIENCE AND EDUCATION
o Preferably hold a diploma from a university or technical college.
o Bachelor’s degree in engineering, Quality Management or a relevant Scientific discipline.
o The education requirement should be a basis for classification of technical knowledge. However, in exceptional cases, a demonstration of equivalent knowledge and skills may be acceptable.
REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS
o Basic experience in the medical device industry and knowledge of ISO 13485 Medical Device Regulation (MDR) Regulation (EU) 2017/745 and ISO 14971 is an advantage
o “Can do” attitude and ability to think creatively and strong organizational skills required
o Organizational Ability: understand what drives decisions, policies, practices, and procedures
o Social skills: ability to work within a team.
o Communication skills: ability to provide, discuss and transfer information in a comprehensible fashion.
o Attention to details
o Organizational ability, play a crucial role in maintaining organized and efficient operations withing the team ensuring control and smooth workflow
o Analytical skills: ability to process and analyze data in a structured manner.
o Problem solving: ability to recognize problems preferably in an early stage and find countermeasures.
o Fluent written and spoken English fluent Dutch is an advantage.
Primary Location Europe/Middle East/Africa-Netherlands-Gelderland-Nijmegen
Organization 8354-GATT Technologies B.V. Legal Entity
Job FunctionQuality Assurance
Req ID: 2406176568W
