* Own the engineering function site-wide, ensuring adherence to all statutory requirements, Good Manufacturing Practices (GMPs), regulations, and company policies affecting engineering integrity and compliance.* Develop and implement engineering strategies aligned with site and corporate objectives, including site space planning and energy conservation initiatives.* Lead and develop a high-performing engineering team (~11 direct reports), fostering a culture of continuous improvement, technical excellence, and professional growth.* Drive change management initiatives within the engineering function and across the site to enhance operational efficiency and effectiveness.* Foster strong working relationships across all site functions and with external partners, promoting collaboration, effective communication, and alignment of engineering goals with broader business objectives. Provide people management through coaching, mentoring, and performance development to build a motivated and capable engineering team.* Lead the Capital Delivery Team responsible for the planning, execution, commissioning, and qualification of all capital projects on site, ensuring projects meet scope, schedule, budget, and quality requirements.* Oversee capital contractor management and ensure compliance with all regulatory and company standards during project execution.* Plan and implement asset recapitalization strategies to maintain and enhance site infrastructure and equipment in line with business goals.* Collaborate with Health, Safety, and Environment (HSE) team to proactively address all engineering-related safety and environmental concerns.* Ensure facility security meets corporate requirements and supports safe, compliant operations.* Maintain compliance with all statutory and regulatory requirements, including timely completion of tests, inspections, and certifications.* Bachelor’s degree in Engineering is required; Master’s degree preferred.* 7-10 years’ experience in Animal Health, Pharmaceuticals, Fine Chemicals, and/or Food Industry.* Professional Engineer designation or equivalent professional qualification required.* Strong understanding of engineering regulations relevant to the site’s geographies.* Proven analytical thinking and troubleshooting skills.* Strong oral, written, and interpersonal communication skills.* Demonstrated ability to work independently and be a self-starter.* Proven ability to multi-task with strong attention to detail.* Experience in validation activities related to aseptic processes, technology transfer, and process validation.* Experience with the design, operation, maintenance, and/or regulatory compliance of pressure vessels in a GMP manufacturing environment.* Familiarity with FMEA (Failure Mode and Effects Analysis), QRM (Quality Risk Management), P&ID (Piping and Instrumentation Diagrams), and PFD (Process Flow Diagrams) development.* Experience in fermentation and cell technology equipment.The Company is required to provide a reasonable estimate of the salary range for this job in certain provinces within Canada. Final determinations with respect to salary will consider a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education. Expected CAD salary range: $ 97,600- $ 165,900. Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, and vacation.**Secondary** **Language(s) Job Description:*** Baccalauréat en génie est requis; Maîtrise de préférence.* 7 à 10 ans d’expérience dans les secteurs de la santé animale, des produits pharmaceutiques, des produits chimiques fins et/ou de l’industrie alimentaire.* Titre d’ingénieur professionnel ou qualification professionnelle équivalente exigée.* Bonne connaissance des réglementations d’ingénierie applicables aux zones géographiques du site.* Compétences avérées en analyse et résolution de problèmes.* Excellentes compétences en communication orale, écrite et interpersonnelle.* Capacité démontrée à travailler de manière autonome et à prendre des initiatives.* Aptitude à gérer plusieurs tâches simultanément avec une grande attention aux détails.* Expérience dans les activités de validation liées aux procédés aseptiques, au transfert de technologie et à la validation des procédés.* Expérience dans la conception, l’exploitation, la maintenance et/ou la conformité réglementaire des équipements sous pression en environnement GMP.* Connaissance des outils FMEA (Analyse des Modes de Défaillance et de leurs Effets), QRM (Gestion des Risques Qualité), P&ID (Schémas de Tuyauterie et d’Instrumentation) et PFD (Schémas de Flux de Processus).* Expérience avec les équipements de fermentation et de technologie cellulaire.L’entreprise doit fournir une estimation raisonnable de la fourchette de salaire pour ce poste dans certaines provinces du Canada. Les déterminations finales concernant le salaire prendront en compte un certain nombre de facteurs, qui peuvent inclure, mais sans s'y limiter, le lieu de travail principal et les compétences pertinentes, l'expérience et l'éducation du candidat choisi. Échelle salariale attendue en CAD: $ 97,600- $ 165,900. Les avantages disponibles comprennent l'éligibilité aux primes, des incitations à long terme le cas échéant, des avantages en matière de soins de santé et d'autres assurances (pour l'employé et sa famille), des prestations de retraite, des congés payés et des vacances. #J-18808-Ljbffr