Director, Process Engineering

AbbVie Inc.; Cork; Presencial; EUR 140.000 - 180.000; Jornada completa

Descripción de la vacante

AbbVie in Ireland is seeking a Director of Process Engineering to lead a technically diverse team responsible for the manufacture of pharmaceutical products. The role bridges development and operations, driving site-wide process improvements and ensuring regulatory and quality compliance.

You will collaborate with Manufacturing and Quality, manage budgets and timelines, and mentor staff while representing the site in audits.

Formación

• Bachelor's degree in engineering (Mechanical, Electrical or Chemical) required.
• 10+ years' experience in the pharmaceutical industry formulation.
• 4+ years of managerial experience.
• Knowledge of AbbVie Engineering standards.
• Demonstrated leadership and team-building skills.
• Strong problem-solving abilities.
• Proven track record of managing projects through to completion.
• Excellent communication skills with layers of management.

Responsabilidades

• Communicates and collaborates with internal and external partners to provide technical and business leadership.
• Maintain and direct a cross-functional staff to ensure CMC lifecycle activities are completed on time and to standards.
• Develops engineering objectives and strategies for site progress and cost optimization.
• Provide leadership, coaching, training, and mentoring to direct reports.
• Represent AbbVie during audits and regulatory interactions.

Conocimientos

Leadership

Communication

Project management

Problem-solving

Educación

Bachelor's degree in engineering (Mechanical, Electrical or Chemical)

Descripción del empleo

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

The Process Engineering department supports technical and scientific activities related to the manufacture of pharmaceutical products in AbbVie facilities or in contract facilities. The Director, through his/her section managers and direct reporting lines, will manage a technically diverse staff of highly specialized engineers and scientists. He/she is a key link between development organizations and operations/third party contract manufacturers and ensures a seamless link between pilot scale and full-scale manufacture. The director is accountable for all the activities of the department and provides technical/scientific and business leadership for the department. The director partners with manufacturing and quality in the identification, definition, and execution of projects and delivers technical requirements for the launch of products and supports the development of innovative solutions to problems and opportunities.

Responsibilities

• Communicates and collaborates with internal (manufacturing, quality, engineering, S&T and other areas) and external partners to provide effective technical and business leadership in line with site goals and objectives.
• Maintain and direct a highly diversified cross functional staff of professionals to ensure that all aspects of CMC life cycle management are completed on time, within budget and meet highest scientific, regulatory, quality, marketing and commercial standards
• Develops engineering objectives and strategies that advance the site, and continually looks for opportunities for process optimization, cost avoidance and cost reduction.
• Develop and communicate cost estimates, business plans, timelines and contingency plans to accomplish project and departmental objectives within agreed time scope.
• Participate in capital plan input and capital project execution to advance manufacturing capabilities
• Make final decisions related to project responsibilities
• Represent AbbVie during audits to regulatory agencies (US/ROW as appropriate) by supplying verbal or written information with active participation.
• Responsible for ensuring that all members of the Engineering team follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition.
• Provide leadership, coaching, training, and mentoring to direct reports. Negotiates, secures, oversees and ensures that all resources are available to meet the demands of the projects and site goals.

Qualifications

• Bachelor's degree in engineering discipline (Mechanical, Electrical, Chemical) is required to provide technical expertise.
• 10 + years' experience in the pharmaceutical industry formulation, including at least 4+ years of managerial experience.
• Knowledge of AbbVie Engineering standards.
• Demonstrated leadership and team building skills.
• Strong problem-solving abilities.
• Proven track record of managing projects through to completion.
• Excellent communication skills with layers of management.

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html