Senior Supplier Quality Engineer

Teoxane Laboratories were established in Geneva, Switzerland, in 2003. They are specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and dermocosmetics. Teoxane strength is to offer a global patient care. Using its products, practitioners are able to fill all kinds of wrinkles, from the finest to the deepest, to restore youthful volume to the face, and to treat the neck and décolleté, with natural results. The strength of Teoxane is also its human size and independence. Teoxane has a total freedom of thoughts, action and innovation which makes the company unique.

In the frame of the growth of our business, we are looking for a:

Senior Supplier Quality Engineer
 

Main Activities

• Supplier Management: Maintain and implement supplier management processes to ensure strong and effective relationships.
• Selection and Evaluation: Participate in the selection, qualification and periodic evaluation of suppliers according to established procedures.
• Complaints and Notifications: Ensure the processing and follow-up of supplier complaints and change notifications within the required timeframes.
• Assessment Meetings: Organize and participate in change impact assessment meetings.
• Audits: Plan, organize and carry out supplier and distributor audits.
• Quality: Handle quality events (non-conformity, OOS, change control, CAPA) in collaboration with other departments.
• Continuous Improvement: Lead problem-solving groups and support continuous quality improvement projects.
• Internal Communication: Feed back information from the various departments within the Quality Department.
• Quality Referent: Intervene on projects as a quality referent, review new design specifications and provide your input on component quality and manufacturing feasibility.
• Investigations and Corrective Actions: Investigate supplier material failures and develop corrective action plans if necessary.
• Acceptance Criteria: Develop material acceptance criteria and activities.

Profile

• Mastery of Quality Standards ISO 9001 & 13485
• Knowledge of MDR
• Certified Lead Auditor 13485
• Knowledge of Quality tools (5P, 5M, 8D,...) and risk analysis methods
• English: Good comprehension and writing skills (minimum level B2)
• Basic training: CFC or equivalent
• Professional experience required: Minimum 5 years of experience in quality in the pharmaceutical and/or medical device industry
• Autonomous, rigorous, with a strong team spirit

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TEOXANE promotes equal opportunity and places at the heart of its human resources management policy the fight against all forms of discrimination based on age, gender, origin, disability, or any other personal characteristic.