Senior Program Manager

PowerToFly; Gallicano nel Lazio; In loco; EUR 130.309 - 156.371; Tempo pieno

Vantaggi offerti da questo lavoro

Medical/dental/vision insurance

401(k) plan

Paid time off and bonus programs

Descrizione del lavoro

AbbVie is seeking a seasoned ME&C Program Manager to lead large, cross‑functional global projects across manufacturing sites. You will coordinate R&D, PDS&T, QA, Supply Chain and Regulatory activities to ensure successful tech transfer and commercialization of oncology biologics products.

The role requires extensive program management experience, GMP knowledge, and the ability to drive complex decisions across functions. Biologics experience is essential for this position.

Competenze

• 10+ years in process development, project management, engineering/process support and manufacturing.
• Strong knowledge of GMP Manufacturing, Supply Chain, Validation, Engineering and regulatory requirements.
• Excellent organizational, planning and communication skills.
• Proven ability to deliver projects with cross-functional teams.
• Multilingual abilities are a plus.

Mansioni

• Assemble and lead matrixed cross-functional teams for process development, manufacturing, QA and QC across multiple sites.
• Lead site transfers, new indications, new presentations and lifecycle projects for oncology biologics on time and within budget.
• Identify and resolve technical and project issues, driving decisions with stakeholders.
• Manage multiple projects concurrently with minimal supervision.
• Develop contingency plans and manage prioritization across competing timelines.
• Present project status to Operations leadership and stakeholders.
• Set project plans, timelines, and budgets to meet business objectives.

Conoscenze

Project management

Process development

Engineering

Cross-functional leadership

GMP knowledge

Biologics

Formazione

PMP certification

Strumenti

GMP expertise

Descrizione del lavoro

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 atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

Job Description

Purpose:

The ME&C (Manufacturing, Engineering & Contracting) Program Manager is an experienced leader responsible for managing large global projects across disciplines and multiple manufacturing locations. This person has previous project management experience and is working on expanding into managing various projects.

This individual provides leadership and coordinated project management for all manufacturing and/or technical activities needed to ensure successful tech transfer and commercialization of the assigned products by integrating the efforts of R&D, PDS&T, Quality, Supply Chain, Regulatory.

This position specifically supports Oncology programs and will require Biologics experience.

After product launch, this individual is responsible for managing the capacity strategy for the product, assurance of supply programs and cost reduction initiatives across the network.

Responsibilities:

• Assemble and lead matrixed cross-functional teams comprised of scientist and engineers responsible for all operational aspects of process development, manufacturing, quality assurance and quality control spanning multiple sites
• Implement site transfers, new indications, new presentations and lifecycle projects for on market programs on time and within budget for Oncology biologics programs
• Proactively identify and drive technical and project plan related issues to closure by working with all relevant functional lines and effectively troubleshooting and driving decisions
• Manage multiple projects concurrently, operating with minimal supervision
• Understand project drivers, requirements, scenarios and options. Proactively drive development of contingency and/or risk mitigation plans.
• Manage competing timelines and make difficult decisions regarding priorities among projects.
• Effectively communicate and present project status to Operations senior management and stakeholders
• Accountable for setting program and project plans, including timelines and expenses, that meet business and organizational objectives and ensuring those plans are achieved.
• Define budget requirements and report monthly actuals, LBE, and Plan/LRP schedules per financial schedule

Qualifications

Qualifications:

Bachelor’s Degree in Engineering, science, or closely related discipline, or equivalent technical experience plus demonstrated competence

• 10+ years of combined experience in positions related to process development, project management, engineering/process support and manufacturing
• Must have strong knowledge of GMP Manufacturing, Supply Chain, Validation, Engineering, CMC technical development and pharmaceutical regulations
• Must have demonstrated organizational and planning skills, excellent verbal and written communication skills
• Must have demonstrated strong project management skills with successful delivery of projects
• Must be able to effectively facilitate the resolution of complex scientific, technical, analytical and business issues across functional lines
• Plant experience a must
• PMP certification a plus
• Proficiency in multiple languages a plus

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
• This job is eligible toparticipatein our long-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company's sole andabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable law.

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, visithttps://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

What AbbVie Has to Offer

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.