Associate Director, Transformation Program Management

Allergan; North Chicago (IL); On-site; USD 137,500 - 261,000; Full time

Benefits offered by this job

Comprehensive benefits package

401(k) plan

Paid time off

Job summary

A global biopharmaceutical company seeks an Associate Director, Transformation Program Management in North Chicago. The role involves overseeing quality assurance for complex products in a high-volume environment while managing a team. Candidates should have 15+ years of experience in the pharmaceutical industry, strong leadership skills, and a Bachelor's degree in a relevant field. The position offers a competitive salary range between $137,500 and $261,000, along with comprehensive benefits. ADA compliance is emphasized.

Qualifications

• Minimum Bachelor's degree required; Master's or PhD preferred.
• 15+ years of experience in Manufacturing and QA in pharmaceutical/biologics.
• Basic understanding of the physical and chemical characteristics of products.

Responsibilities

• Responsible for quality assurance at a high-volume plant.
• Manages a team and ensures compliance with corporate Quality requirements.
• Communicates with executive level on Quality Management Review.

Skills

Leadership

Communication Skills

Quality Assurance

Regulatory Compliance

Statistical Quality Systems

Education

Bachelor's Degree in Physical or Life Sciences, Pharmacy or Engineering

Master’s Degree or PhD

Certified Quality Engineer

Tools

Electronic Document Management

Laboratory Information Management

Job description

Associate Director, Transformation Program Management

• Full-time
• Salary Min: 137500
• Salary Max: 261000
• Workday Global Grade: 20
• Compensation: USD 137,500 - USD 261,000 - yearly

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 ,X andYouTube.

The Associate Director, Quality provides leadership and direction to the Quality Function they are responsible for within Operations. This Associate Director, Quality is responsible for the effective implementation of AbbVie Quality Systems for which they are responsible for. This could include: Incoming Quality Assurance of drugs and packaging materials, Manufacturing Quality Assurance, Validation of product and processes, Quality Engineering, Quality Control, Training, Regulatory Compliance, Quality Planning, Product Quality and strategic initiatives. The Sr. Manager of Quality would be expected to manage a budget and leads a team of quality professionals who are responsible for compliance and quality oversight for the plant and/or strategic initiatives. Expectations that the professional will maintain high quality levels on all products while achieving high efficiency.

Responsibilities

• Responsible for various aspects of quality assurance and quality control related to products produced at the plant. This will be at a large plant with high volume, high level of product complexity including multiple products at the site and may have the complexity of multiple types of productions (API, Fin Goods, Biologics, Packaging, Device, etc.).
• Represents the decision-making authority on job specific aspects of the Quality and Regulatory compliance program for the site.
• Ensures that product within the plant is consistently manufactured in conformance with corporate Quality requirements and all applicable regulatory requirements.
• Manages a team of quality professionals. Directly responsible for the effective organization, administration, training and supervision of their functional area.
• Provides regulatory and technical guidance to all departments in the plant and can be the SME for all AbbVie plants.
• Communicates with executive level for Quality Management Review, Quality Initiatives, etc.
• Responsible for the development and administration of the annual operating budget for the Quality Unit they are responsible for.
• Incumbent is responsible for quality decisions related to all aspects of the plant operation including facility design, laboratory controls and product specifications and to ensure that the area of their responsibility meets all cGMP, FDA, EU, DEA and other regulatory requirements.
• Manages a team in the Quality Function to include hiring, setting performance expectations and performance assessment.

• Minimum Bachelor’s Degree required preferably in Physical or Life Sciences, Pharmacy, or Engineering; Master’s Degree or PhD preferred.
• Certified Quality Engineer or formal training in quality engineering or statistics is preferred
• 15+ years of combined experience in Manufacturing, QA, QC, R&D in pharmaceutical, biologics, device or chemical industry
• Must have a basic understanding and working knowledge of the physical and chemical characteristics of the products, including raw materials, manufactured at the plant.
• Must be familiar with use of statistical quality systems, electronic document management and laboratory information management.
• Must also be familiar with Quality policies as well as cGMP and other regulatory requirements.
• Must have effective people management and communication skills necessary to supervise those reporting directly or through subordinates as well as establish and maintain effective working relationships among other key individuals in manufacturing, materials management, engineering, product development, Quality Systems, Product QA, Quality Control, Information Systems and Regulatory Affairs and must demonstrate sound judgment in evaluating and acting on day-to-day situations.
• Strong communication Skills, both oral and written
• 10+ years of supervisory/technical leadership experience

Applicant notes

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

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 this posting 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.

We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.

This job is eligible to participate in our short-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 and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable 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.

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