Associate Director, Quality Control Laboratory

Allergan; North Chicago (IL); On-site; USD 80,000 - 130,000; Full time

Job summary

An established industry player is seeking a dynamic leader to oversee laboratory operations and quality control. This role involves managing a talented team, ensuring compliance with regulatory standards, and driving continuous improvement initiatives. You will play a pivotal role in advancing scientific research and operational excellence, while fostering positive relationships with stakeholders. If you are passionate about leading teams and making a significant impact in the field of health care, this opportunity is perfect for you. Join a forward-thinking organization that values innovation and integrity, and be part of a mission to improve lives through science.

Benefits

Paid Time Off

Medical/Dental/Vision Insurance

401(k) Plan

Short-term Incentive Programs

Long-term Incentive Programs

Qualifications

• 10+ years of experience in laboratory operations management required.
• Strong understanding of regulatory compliance and quality control.

Responsibilities

• Lead and develop a team of managers and analysts in the QC lab.
• Ensure compliance with government regulations and corporate practices.

Skills

Laboratory Operations Management

Technical Writing

Problem Solving

Budget Management

Regulatory Compliance

Team Leadership

Education

Bachelor's Degree in Science

Master's Degree in Science

PhD in Science

Job description

Company Description

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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedIn, andTik Tok.

Job Description

Purpose

Will typically serve as the head of the laboratory operations for the plant. Responsible for management of the QC Laboratory organization which may include management of Managers, Supervisors and Analysts. Manages a business unit consisting of one of the following disciplines: API Laboratory Operations, Finished Goods Laboratory Operations, Raw Material/ In-Process Laboratory Operations, Laboratory Support Operations, and Laboratory Continuous Improvement/Compliance Operations.

Responsibilities

• Manage a team of Managers, Supervisors and Lab Analysts. Responsible for hiring, leading, and developing team members to ensure that the department has the appropriate talent and level of performance to meet business objectives. Assure training and development of subordinates. Assist subordinates in problem solving. Identify and resolve people issues without direct supervision.
• Assure conformance to all government and corporate regulations. Responsible for developing, providing, defending, and persuading Corporate/Plant practices with outside organizations. Routinely meet with regulators (FDA & EU) and customers to ensure no interruption in business due to compliance issues.
• Direct area of responsibility to meet production objectives within planned budgets. Provide input to manager for resources needed to construct budget, updates, and changes in financial plan. Manage area supplies and equipment within budgeted amounts.
• Establish and execute plans and commitments consistent with Development, Manufacturing, Customers, and Business needs.
• Conceive, design, conduct, and advance independent scientific research activities per strategic business needs. Ensure research activities/projects are on track per business needs and established timeline.
• Develop, negotiate, and finalize timeline and cost estimates for projects and/or service contracts to support business operations and/or external customer’s needs.
• Conceive, design, and execute projects related to the strategic needs of the business operations.
• Provide timely testing or execution of in-process, raw materials, intermediates, API, finished goods, continuous improvement initiatives, QA training, laboratory equipment validation, and stability depending on area of responsibility.
• Apply advanced technical writing skills to prepare project protocol and final reports to support product registration and/or business needs.
• Conduct business and interact/ negotiate with external contacts and customers to develop positive business relationships.

Qualifications

Qualifications

• Required - BS degree in Science or equivalent and 10+ years of relevant experience OR Master's degree in Science or equivalent and 8+ years of relevant experience. Preferred - PhD in Science or equivalent and 6+ years of relevant experience.
• Must be experienced and demonstrate a high level of technical skill in lab operations and a good understanding of related business.
• Related knowledge in Product Quality, Quality Control Lab Operation and Regulatory requirements is required.
• Ability to work independently to meet operational goals and business needs.
• Ability to develop, design, execute, and manage complex research programs.
• Ability to make operational and business decisions with minimum direction from immediate manager. Must have knowledge and skill in personnel management, and developing and managing budgets.
• Ability to interact and establish positive interaction with internal/external customers.
• Shows broad understanding of the issues relevant to technical/science and business.

Key Stakeholders

Development, Manufacturing, Quality, MS&T, and Regulatory

Additional Information

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.
• 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 remain 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, serving our community, and embracing diversity and inclusion. It is AbbVie’s 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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