At Werfen in Clinical Software Business Unit we are committed to developing secure, efficient, and innovative clinical applications and laboratory instrumentation systems. Our solutions enhance patient care and facilitate the management of information in hospitals and laboratories around the world.
Solutions QA Leader focuses on organizational aspects of quality management, aiming to improve the end-to-end product development life cycle, from requirements analysis to launch and maintenance. Working closely with the Solutions Leaders to ensure to deliver software releases with an ever-increasing level of quality.
When applicable, QA Customer Liaison facilitating effective communication and understanding of QA processes, methodologies, and outcomes.
Key Accountabilities
Be a key part of a team where you will:
* Cooperate with the Director of Quality & Regulatory Affairs - Digital Solutions to coordinate quality assurance activities for all SW development products assigned.
* Be responsible for ingraining quality as a core discipline into every aspect of the SW development teams (Squads) organizations.
* Ensure that SW Development teams (Squads) are informed with the perspective of the QA processes and/or customer requirements enabling the delivery of a product or service to an agreed level of quality.
* Oversee SW project documents subject to QA approval ensuring the establishment and adherence to the appropriate QMS and customer processes and procedures, including but not limited to requirements management, configuration control, secure design, risk analysis, verification and validation, traceability, etc.
* Support Change Management Board (CRB) process as needed.
* Advance metrics and the setting of goals that provide visibility and understanding of development effectiveness from a quality perspective.
* Drive and promote continuous improvement initiatives to enhance product quality, operational efficiency, and customer satisfaction.
* Collaborate in the QS software development life cycle procedures definition and maintenance. Provide input in the implementation of the process.
* Be the point of contact for the different business unit's/client related with Quality agreements.
* Take an active role in the training and dissemination of knowledge regarding quality system procedures.
* Pursue a unified approach to quality process implementation throughout the software development lifecycle across all solutions within a Factory.
* Participate in software products audits and assessments as needed.
Networking/Key Relationships
The main relationships within the Werfen Group are:
* Factory Lead and Solution Leaders
* Solutions QA Leaders from other factories
* SW Development Teams (Squads) and Chapter Leads
* QARA Manager and QARA Specialist
* Customer
* Application Lifecycle Manager (ALM)
* This position may also require cooperation with other companies inside Werfen.
Minimum Knowledge & Experience Required for the Position:
Education: Engineer, Computer Science or other Technical degree, or equivalent work experience.
Experience:
* A minimum of 5 years of experience in a QA related role.
* Knowledge in SW Development methodologies preferably within the Healthcare sector.
* Experience in the creation or revision of comprehensive software products documentation.
Additional Skills/Knowledge:
* Knowledge about applicable standards and regulations related to SW development for Health and/or Medical Device (ISO 13485, ISO 14971, IEC 62304, IEC 82304, ISO 62366, cybersecurity).
* Familiar with medical device regulations (MDR/IVDR, FDA, etc).
Skills & Capabilities:
This position has a combination of technical and leadership experience in QA area being able to collaborate seamlessly with cross-functional teams for ensuring product quality and customer and regulatory compliance. The role requires adaptability to evolving technologies, strong communication skills, and a commitment to fostering a quality-focused culture within the organization.
Besides, it is needed to have:
* Strong interpersonal skills with a proven ability to collaborate across teams and communicate effectively with stakeholders.
* Flexibility and adaptability to a fast-changing environment/methodology.
* Self-organized and self-monitor to be able to report the effort dedicated to each individual task inside all the different responsibilities.
* Good level of Technical and Conversational English.
* Commitment to continuous improvement, with a track record of implementing initiatives to enhance overall quality processes.
What We Offer:
* A meaningful project that will impact the quality of laboratory software medicine worldwide.
* 3 days a week working from home.
* Multicultural and friendly team.
* Exciting opportunities for professional development.
* Ongoing training.
* Social benefits: Canteen, nursery check, English training...
* All the benefits according to the chemical agreement.
Our Purpose: We contribute to the advancement of patient care around the world through innovative specialized diagnostics.
JOIN US!
Seniority Level
* Mid-Senior level
Employment Type
* Full-time
Job Function
* Industries: Software Development
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