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 at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Job Description
Join our team at AbbVie, as a Laboratory Supervisor in our Central Services QC Laboratories on our Westport site. Reporting directly to the Senior Manager, Central Services QC Labs, you will lead a dedicated team of 8-12 direct staff members. In this pivotal role, you will be responsible for overseeing the QC Laboratories Stability & Data Management Team. Your leadership will ensure the alignment and improvement of our data systems, including LIMS systems, LabX and MODA, as well as the setup and maintenance of the Westport Stability Program. Collaborating closely with New Product Introduction groups and other manufacturing units, you will develop and maintain stability master documents that meet all regulatory requirements.
Responsibilities:
- Lead and guide the Stability & Data Management Team to ensure timely and GMP-compliant completion of activities in line with regulatory and corporate standards.
- Develop and maintain strong relationships with management, colleagues, and customers across various business units and project teams.
- Oversee project management, including the creation of Gantt charts and managing projects from initiation through to successful completion.
- Motivate the team, addressing performance issues and conducting performance meetings as per company policy.
- Review and approve Stability Master Documents as required
- Manage team attendance and timekeeping, taking corrective action when necessary.
- Actively participate in the training and certification of new employees.
- Ensure adequate staffing within the area of responsibility, managing any constraints effectively.
- Coach and develop team members, supporting succession planning initiatives.
- Act as a subject matter expert during inspections, representing the company as required.
- Drive continuous improvement in the QC laboratories by identifying and implementing efficiencies and quality enhancements.
Qualifications
- Minimum of 3 years of experience in a QC environment within the pharmaceutical industry and proven project management experience.
- Supervisory experience or demonstrated attributes for effective people management.
- Scientific qualification in a relevant discipline with in-depth knowledge of laboratory GMP standards.
- Proficiency with electronic laboratory systems such as LIMS etc.
- Strong communication and conflict handling skills, with the ability to adapt to a dynamic environment.
Additional Information
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, 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
