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Full Time Posted an hour ago
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powertofly approved What AbbVie Has to Offer:

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

Job Details


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 at www.abbvie.com. Follow @abbvie on XFacebookInstagramYouTubeLinkedIn and Tik Tok.


Job Description

We are now hiring a QC Analytical Lab Supervisor to join our team in Abbvie Ballytivnan, Sligo. You will lead the QC Analytical team and ensure the continued success of the team. Ensure that technical and systems excellence is maintained in the laboratory by ensuring own skills are maintained, by coaching and training analysts to ensure right first-time behavior and by implementing improved working practices in terms of efficiency, compliance and Right First Time. 

A snapshot of your key responsibilities: 

  • Supervise Daily Laboratory operations, ensuring personnel execute their responsibilities in strict accordance with relevant regulatory guidelines. Support the weekly and daily production schedules and participate in the daily Tier 1 & 2 meeting. 
  • Ensure Laboratory Documentation and Computerized Systems (LIMS, Empower, LabX) compliance with Data Integrity policies and regulatory requirements. 
  • Supervise the QC Analytical laboratory operations and ensure compliance with regulations including EU Annex 1, ISO, WHO, FDA Guidelines for Aseptic Processing, among others. 
  • Resolving analytical OOS issues as they arise in a timely manner both through practical work and through solTRAQs/OneTrack systems. 
  • Review of results from Clean & Utilities program (WFI/RO/CS water testing), Product Testing (In process and Final product as required) and Analytical Lab (pH, TOC, Conductivity, Osmolality, Density, HPLC, Raman, etc.) activities, results and raw data on time, accurately and legibly. 
  • Participate actively in Laboratory Investigations Reports (LIRs), Invalid results investigation review, approval and creation of effective CAPAs. Initiate and Collaborate with all Out of Specification (OOS) results. 
  • Ensuring 6S excellence is maintained across the Laboratory. 
  • Instilling a quality culture of Zero, Believe it, Achieve it amongst the QC laboratory team. 
  • Lead and contribute to project initiatives to improve laboratory operations and efficiency as assigned by the QC Lab Manager, acting as designee for the Laboratory Manager as assigned. 
  • Work with a cross functional team, Supervisors, Quality Manager and Laboratory Manager to ensure compliance with Quality Management System 
  • Support the training and mentoring of laboratory personnel and contribute to training program development. 
  • Operates in an environment which is essentially self-managed but with supervision through the Laboratory Manager. 
  • Provides supervision to direct reports and be responsible for setting annual goals, completing reviews, growth plans and performance management of the team. 

Qualifications

  • BS in science or equivalent (Chemistry, Microbiology, or Biology preferred) 
  • 2-5 years of laboratory experience 
  • 2-5 years of supervisory experience 
  • Demonstrated skills to deal effectively with members of the department and the areas serviced by the laboratory 
  • Problem solving skills are required 
  • Must be able to interpret impact of laboratory data for appropriate and effective actions 
  • Must be able to identify problem areas requiring development, maintenance, production, engineering, accounting, or planning with assistance from more senior staff 
  • Must also be able to 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 

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

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Supervisor, Laboratory Quality Control
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