Associate Director, Maintenance

🕒 il y a 1 mois

🦀 Maryland – Distant

🦀 Maryland – Remote

💵 $174 000 - $203 000 / an

⏰ Temps Plein

🟠 Senior

👔 Directeur

👻 Score fantôme 5%

Ce que ça veut dire : la probabilité que cette offre reste ouverte sans recrutement actif.Comment le lire : 60 % ou plus, on pense que c'est une offre fantôme. Un score plus bas est moins inquiétant.Comment on la calcule : ancienneté, republications, postes ouverts vs taille de l'équipe, rapidité de clôture, et si le salaire est indiqué.À noter : une estimation à partir de données publiques, pas un jugement sur l'entreprise. De vraies offres peuvent avoir un score élevé, alors prenez-le comme un indice, pas comme un fait.

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Lonza

Site WebLinkedInTous les Emplois

10 000+ employés

Fondée en 1897

🧬 Biotechnologie

💊 Pharmaceutique

🏭 Fabrication

💰 €444 795 339 Post-IPO Debt - Lonza en 2023-11

Biotechnology • Pharmaceuticals • Manufacturing

Lonza est une organisation mondiale de développement et fabrication sous contrat (CDMO) et une entreprise de sciences de la vie basée en Suisse. Elle propose une gamme intégrée de services complets allant du développement et de la fabrication de médicaments biologiques et de petites molécules - y compris le développement de lignées cellulaires, le développement de procédés et d'analyses, la formulation et le conditionnement primaire, la fabrication de substances actives et de produits finis, ainsi que le soutien réglementaire/CMC. Les capacités de Lonza englobent la synthèse avancée et les API (y compris les HPAPI), la bioconjugaison et les ADC, des modalités spécialisées telles que les thérapies cellulaires et géniques, l'ARNm/LNP, les procédés microbiens, ainsi que les produits de capsules et d'ingrédients de santé. Fondée en Suisse en 1897, Lonza se décrit comme un pionnier et un leader mondial dans l'industrie CDMO et opère avec environ 20,000 collaborateurs sur cinq continents pour soutenir les clients pharmaceutiques et biotechnologiques.

Description

• Lead maintenance and reliability readiness activities for a U.S. growth investment project. • Ensure the facility, equipment, utilities, process equipment, and maintenance systems are designed and implemented with long-term reliability, maintainability, mechanical integrity, and GMP compliance in mind. • Work closely with Engineering, Operations, Automation, MSAT, and Quality to establish the maintenance organization, systems, and processes required for successful site start-up and ongoing operations. • Provide maintenance and reliability leadership throughout facility design, construction, commissioning, qualification, and start-up activities. • Develop maintenance strategies, including preventive, predictive, and reliability-centered maintenance programs to support long-term asset performance. • Partner with Engineering and project teams to ensure maintainability, serviceability, accessibility, and lifecycle considerations are incorporated into facility and equipment design. • Establish asset lifecycle management strategies, including spare parts plans, calibration programs, and equipment reliability initiatives. • Support the selection, implementation, and optimization of CMMS and other maintenance technologies to enable effective planning and execution. • Participate in commissioning, qualification, FAT/SAT, and operational readiness activities to ensure maintenance requirements are incorporated and validated. • Define the future maintenance organization, including staffing plans, training requirements, operating procedures, and site support models. • Identify and mitigate equipment reliability, maintenance, and operational readiness risks while providing updates and recommendations to project leadership.

🎯 Exigences

• Bachelor’s degree in engineering, Facilities Management, Reliability Engineering, or a related technical discipline; advanced degree preferred. • 10+ years of experience in maintenance, reliability, engineering, or technical operations within pharmaceutical or API manufacturing environments. • Experience with HPAPI, complex chemical synthesis, or chemical process manufacturing is preferred. • Experience supporting major capital projects, facility start-ups, manufacturing expansions, greenfield or brownfield investments, or large-scale operational readiness initiatives. • Strong knowledge of maintenance best practices, reliability engineering, asset lifecycle management, and equipment performance improvement. • Experience with CMMS platforms, predictive maintenance technologies, reliability-centered maintenance (RCM), and maintenance planning systems. • Understanding of GMP requirements related to equipment maintenance, calibration, qualification, documentation, and inspection readiness and mechanical integrity principles. • Demonstrated experience supporting small molecule drug substance, API, or HPAPI manufacturing operations preferred. • Experience supporting containment-intensive manufacturing environments (e.g., HPAPI containment, isolators, contained material handling) preferred. • Experience within a multi-product API manufacturing or CDMO environment is preferred. • Strong leadership, communication, collaboration, and problem-solving skills with the ability to influence cross-functional teams and stakeholders. • Ability and willingness to transition to an East Coast or Midwest U.S. site location as project needs evolve. • Willingness and ability to travel to EMEA and NA at approximately 25-30% of the time to meet business objectives.

🏖️ Avantages

• Performance-related bonus. • Medical, dental and vision insurance. • 401(k) matching plan. • Life insurance, as well as short-term and long-term disability insurance. • Employee assistance programs. • Paid time off (PTO).