IT Solutions & Cybersecurity Quality Senior Director

A family-owned company, bioMérieux has grown to become a world leader in the field of in vitro diagnostics. For 60 years and across the world, we have imagined and developed innovative diagnostics solutions to improve public health. Today, our teams are spread across 45 countries and serve 160 countries with the support of a large distribution network.

Come and join a family-owned global company with a long-term vision, and a human-centered culture.

We are looking for an IT Solutions & Cybersecurity Product Quality Senior Director who will evolve within the quality department and will report to the Senior VP of pre and postmarket quality.

This position under the supervision of the SVP pre and postmarket quality, is accountable of the quality level of the product range throughout product lifecycle management starting with the support of the development of the product, approval of the product risk analysis files, management of vigilance and field actions activities. The quality product senior director will also be in charge of issuing the Post market quality reports defining if the product is still state of the art and if any support post launch is needed. He provides visibility on the quality level of the product range to the top management and propose action to maintain it at the right level for our customers and patients. He is also in charge of keeping up with bioMerieux growing market and product lines, and the ever-evolving global quality landscape.

The senior director will ensure adherence to policies and drive implementation of the all quality processes especially product risk files, Product Development Process, assessment for potential adverse events, field actions and Post Market Surveillance, as well as compliance with Corporate and external requirements (e.g. applicable standards and regulations, Distributors management).

The manager will build the department in collaboration with the main internal stake holders such as R&D software and cybersecurity teams. He will manage an operational team of less 10 people at the beginning but the objective is to grow the team as this market has been identify as a key one for biomerieux growth. The future structure of the organization when the critical mass will be reached is to have 2 managers in charge of, on one side postmarket quality activities such as vigilance and field actions and one the other side premarket quality activities such as the support of the development of new products and product life cycle management. In addition to the managers, 2 single contributors will be in charge of risk management for the product range and postmarket surveillance reports. The team will be mainly based in France and in the US.

Through the use of strategic thinking, study design expertise, and an ability to navigate and align stakeholders, the senior director will facilitate cross functional approaches to address identified product trends/issues and investigate to ensure proper reporting to executive management and regulatory agencies, continual assessment of benefit-risk ratios and product safety/effectiveness, as well as providing feedback for future development needs. The senior director is a key contributor.

Studies-Experience:

• Master's degree or equivalent in Science or Engineering
• 10+ years in quality vigilance/field actions and or design control, or equivalent, medical device/IVD industry preferred
• Expertise in software development
• 5+ years leading projects and directly managing other employees.
• Excellent verbal and written communication skills.
• Fluent communication in English

Skills and Qualifications:

• Demonstrate success in supporting both growth and product support projects, including complex projects involving ambiguity, in a rapidly changing regulatory and quality environment.
• Comprehensive knowledge of regulations applicable to medical device/IVD industry with an expertise on vigilance, field actions and design control ones. Must be able to interpret regulatory and quality requirements (QSR, IVDR, ISO 13485 / ISO9001 and/or local GMPs if appropriate). Experience in participation in the management of regulatory audits (i.e. ISO 9001, 13485, FDA, etc.); Knowledge in the interpretation and application of relevant Domestic and International Regulations and Industry Standards (e.g. ISO, QSR, UL, CSA, VDE, etc.).
• Ability to inspire, motivate, and build the confidence of teams to reach goals, consistently pushing self and others to achieve results.
• Ability to influence peers, higher leaders and external expert or regulatory bodies.
• Must demonstrate strong leadership skills
• Ability to work both independently and in a team environment.
• Ability to analyze and use data to drive decisions and process improvements. Familiar with product profiles and technology, company organization and processes will be a plus.

Mobility: Travel as needed (external meetings with the local and corporate teams, trainings)

bioMérieux welcomes applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.