Associate Director, Quality Control - Lincoln, United States - Allergan

Description

Company DescriptionAbbVie'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 immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio.

For more information about AbbVie, please visit us at Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Job DescriptionThe Associate Director, Quality Control provides leadership and direction to the Quality Function they are responsible for within Operations.

This Associate Director, Quality Control 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 Associate Director, Quality Control 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.
ResponsibilitiesResponsible 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.
Significant Work Activities

• Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day)QualificationsMinimum Bachelors Degree required preferably in Physical or Life Sciences, Pharmacy, or Engineering; Masters 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.10+ years of supervisory/technical leadership experience.

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 verbaland writtenKey Stakeholders:

Development, Manufacturing, Quality and RegulatoryAdditional InformationAbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.

It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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