Supervisor, Laboratory Quality Control
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Sligo, SO
- Operations
- On-Site
- Full-time
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 – 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.
We are currently seeking a dynamic and detail-oriented Supervisor for the QC Lab located on Manorhamilton Road, Sligo. This pivotal role is responsible for delivering an effective testing and analytical service to ensure that our plant's products consistently meet specified standards. As an important part of the quality control team, the Supervisor will take full accountability for compliance, documentation, equipment maintenance, and training within the QC Lab. This position is ideal for an individual who is passionate about quality assurance and possesses the skills needed to lead teams, optimize lab operations, and ensure that safety and quality standards are not only met but exceeded.
- Ensure Laboratory Documentation and Systems comply with Data Integrity policies.
- Understand and apply Regulations for Laboratory Data Integrity.
- Coach and guide analysts to optimize performance.
- Boost team efficiency and adhere to compliance timelines.
- Collaborate with the lab manager to enhance laboratory performance.
- Resolve analytical deviations promptly.
- Maintain 6S excellence and promote a quality culture.
- Ensure proper equipment use and maintenance.
- Support lab projects and develop procedures.
- identify problem areas requiring development, maintenance, production, engineering, accounting, or planning with assistance from more senior staff
- Identify, communicate, and follow-through to completion and assist in the development of necessary corrective action plans to resolve the problem with supervision. May also assist in the activities required for the investigation and resolution
- Comply with EHS standards and Compendia testing requirements.
- Conduct document reviews and develop training materials.
- Oversee equipment calibration and team performance management
- Bachelors degree in science (Chemistry preferred)
- 4+ years of analytical experience in the pharmaceutical industry
- Expertise in HPLC, GC, LCMS, GCMS, and other analytical techniques.
- Strong regulatory knowledge and experience with analytical equipment.
- Excellent interpersonal kills to deal effectively with members of the department and other teams supported by the laboratory
- Problem solving skills with the ability to interpret impact of laboratory data for appropriate and effective action.
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
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Pay Range: $
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Where We Work
Role is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.