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Supervisor I, QC Lab

External
Abbvie logoAbbvie · Waco, TX
Full-timeOn-site2d ago
ComplianceLessNegotiationTechnical Writing
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Responsibilities

  • Oversees the operation and functions of the laboratory group which may include Raw Materials, Finished Products, Projects/validation samples, and environmental monitoring.
  • Identifies aspects of the tests or results warranting further attention and implements corrective actions.
  • Reviews and approves data (may relate to analytical product release depending on regional regulatory requirements).
  • Supports laboratory investigations, including out-of-specification test results, and ensures effective corrective actions are implemented.
  • Effectively understands, communicates, and presents QC Metrics. Attends and leads Tier meetings.
  • Ensures appropriate procedures are in place and that QC activities are executed in line with internal procedures, requirements of cGMP, and relevant safety standards. Assists in implementing continuous improvement actions to lab processes.
  • Assists in the periodic inspection of laboratory facilities to ensure that they are operated and administered according to Good Manufacturing Practices (GMP) and Good Laboratory Practices, maintaining laboratory audit readiness. When required, support supplier, internal, and regulatory audits
  • May serve as a backup when the Lab Manager is unavailable. Generates and manages non-hazardous and hazardous waste, according with the internal operating procedures and in compliance with local and federal regulations.
  • Bachelor's Degree required, preferably in a Scientific field (Chemistry, Microbiology, or Biology)
  • 2+ years of QC Lab experience required.
  • Demonstrated thorough scientific knowledge and technical expertise in chemistry, technical writing, investigations, analytical laboratory equipment, and laboratory operations required.
  • General knowledge in cGMPs, compendia, and regulations required
  • Effective problem-solving, decision-making, teamwork, influence, negotiation, and conflict resolution skills required. Ability to foster an inclusive environment.
  • Ability to work cross-functionally and coordinate work both within the department and with other departments.
  • Ability to interpret the impact of laboratory data for appropriate and effective actions.
  • Ability to identify, develop, communicate, and follow through to completion necessary corrective action plans to resolve problems.
  • **This is a 3rd Shift position. Hours: 5:45pm-6am
  • Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • 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

Benefits

Dental insuranceVision insurance401(k)Paid time offPerformance bonus

Additional Information

The QC Lab Supervisor I is responsible for the organization, administration, and supervision of Lab Analysts and other Lab employees; properly overseeing the day-to-day operations by prioritizing shop floor presence and receiving guidance and direction from more senior leaders. Oversees the processes of the chemical analysis and release of raw materials, in-process, and final products in compliance with current quality criteria while respecting deadlines and managing costs. Ensures effective and efficient utilization of laboratory resources through management of laboratory support activities.


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