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Purpose
The Director, Program Management will be responsible for the overall program and project management governance and oversight across ME&C (Manufacturing Engineering & Contracting). The role will drive standardization and alignment across the various PM organizations at the site and global ME&C level while also having responsibility for implementation and oversight for assigned manufacturing programs within the ME&C. With this role being a new position, the individual will have the ability to design and implement the new governance and project management processes.
The individual will be required to lead a broad cross-functional team to ensure all programs and projects have the right prioritization, governance and structure while also ensuring proper funding is achieve. The individual must have the ability to work independently, with a strong technical and manufacturing background that can enable program execution. The individual should also operate as an effective and engaged leader where they will enable business strategy, lead program governance, stakeholder engagement and communication to senior leadership.
Responsibilities
- Define and roll out project governance and prioritization processes across multiple cross-functional teams and ME&C sites, ensuring alignment to ME&C and regional strategies
- Define and roll out the standard set of templates and tools to be used across the ME&C PM organization
- Develop and report metrics and dashboards to track and display progress of programs/projects
- Establish and manage the ME&C Program management COP
- Lead and direct multiple cross-functional teams for the implementation of complex programs, managing strategy, execution and budget.
- Ensure effective communication within team and to Senior Leader stakeholders.
- Develop and coordinate standard PM training for the organization both global and site-based
- Manage the ME&C Strategy team communication tools including Teams and Sharepoint
- Communicate program requirements, priorities and decisions, regularly and effectively.
- Manage a staff of 1-3 and ensure the successful implementation of their programs
- Bachelor in Science or Engineering; MBA or Ph.D preferred.
- Strong knowledge of GMP Manufacturing, Supply Chain, CMC technical development and pharmaceutical regulations is required.
- Demonstrated strong planning and project management skills while managing large, complex programs in the pharmaceutical industry.
- PMP certification a plus.
- •10+ years of industry experience, 5 or more years program management experience.
- Strong strategic thinking and leadership skills.
- Strong communication, organization, analytical, presentation, and people skills.
- Demonstrated experience in a global and multi-cultural environment.
- Proven ability to resolve conflict across cross-functional teams and technical experts.
- Ability to understand technical aspects of complex systems and guide cross-functional and detailed technical discussions during critical problem solving exercises
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
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The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of thisposting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future.
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We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
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This job is eligible to participate in our long-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
Abb Vie 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
About Abb Vie
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.
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AbbVieについて

AbbVie
PublicPharmaceutical company.
10,001+
従業員数
North Chicago
本社所在地
$200B
企業価値
レビュー
3.2
10件のレビュー
ワークライフバランス
3.2
報酬
4.1
企業文化
2.8
キャリア
2.9
経営陣
2.3
45%
友人に勧める
良い点
Good compensation and benefits
Strong leadership potential
Good work-life balance and flexibility
改善点
Toxic work environment
Poor management and leadership issues
Frequent policy and organizational changes
給与レンジ
88件のデータ
Mid/L4
Senior/L5
Staff/L6
Mid/L4 · Associate Business Systems Consultant
4件のレポート
$191,100
年収総額
基本給
$147,000
ストック
-
ボーナス
-
$160,364
$192,815
面接体験
4件の面接
難易度
3.0
/ 5
期間
14-28週間
体験
ポジティブ 0%
普通 25%
ネガティブ 75%
面接プロセス
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Panel Interview
5
Offer
よくある質問
Behavioral/STAR
Past Experience
Culture Fit
Technical Knowledge
ニュース&話題
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3d ago
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4d ago
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24/7 Wall St.
News
·
4d ago
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UChicago Medicine
News
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6d ago