Process / Product Engineer M/F
About AbbVie AbbVie's mission is to discover and produce innovative medicines that provide solutions to today's serious health problems while meeting tomorrow's medical challenges. We seek to transform people's lives in several key therapeutic areas such as immunology, oncology, neuroscience, ophthalmology, virology, in addition to the products and services within our Allergan Aesthetics portfolio. We are proud to be a Great Place to Work company.
Join us by joining the 3rd largest pharmaceutical laboratory in the world and a growing site between lakes and mountains! A leader in medical aesthetics, Allergan, a subsidiary of the AbbVie Group, develops and manufactures sterile injectable products based on hyaluronic acid for aesthetic facial treatment, thereby contributing to patient well-being. Our ambition? To offer the best innovation in the aesthetic medicine market. To support our strong growth, we are recruiting for our Engineering Department: A Process / Product Engineer on a fixed-term contract (CDD) for a duration of 18 months This mission will suit anyone wishing to evolve within a multicultural organization combining agility, commitment, and speed of action. You will provide the necessary technical support to Operations for the conduct and improvement of manufacturing processes for products in the sector. Gel You know the critical process parameters and their influence on the product and act as the process referent during investigations, audits, or change impact assessments. You will bring us your ability to: Provide daily support to the production department: participation in CAP and production cell meetings, field presence; proposing and implementing return-to-standard or improvement actions, conducting investigations. As part of projects/initiatives to improve an existing manufacturing process: Define the change strategy Evaluate technical feasibility Define and Lead potential experimental plans and write associated reports Evaluate impacts on critical process parameters and product attributes Participate in the development of process validation documentation as a technical representative Support the execution of validation tests Supervise and/or perform the update of associated operational documentation Ensure staff training on the implemented change Plan your activity and participate in team meetings Communicate progress to the project manager Close your activity and formalize the feedback/lessons learned Lead the project (cross-functional team animation, reporting, progress monitoring) while mastering Quality, Cost, Deadline, Content, and Resource dimensions
Coordinate changes (change control) in your sector and manage the work in progress. Maintain / Create process documentation for the sector Ensure the appropriate level of knowledge for users (production / quality / methods) regarding processes Act as the sector's process referent for impact assessments, document review/approval, investigations, audits, etc. Ensure the monitoring of production start-up phases (ramp-up) for new processes in your sector.
You possess assets to join us: A Master's degree (Bac + 5) in process engineering, biological engineering, or equivalent. A minimum of 5 years of experience in a similar position in a pharmaceutical or medical device industry Experience in project management and knowledge of project best practices. Mastery of problem-solving tools (DMAIC/A3/5M) Knowledge in process engineering, rheology, chemistry, statistics Knowledge of quality requirements relating to the manufacture of medical devices, good documentation practices, and the ISO environment Fluency in English Listening, analysis, and synthesis skills Good ability to work in a team Sense of planning and organization A strong capacity for adaptation, versatility, and openness to change
AbbVie is an equal opportunity employer and is committed to acting with integrity, stimulating innovation, transforming lives, and serving our community. Equal opportunity employer for veterans and people with disabilities.