Supervisor, Laboratory Quality Control

Sligo - Ireland

Monthly Salary: Not Disclosed

Posted on: 13 hours ago

Vacancies: 1 Vacancy

Job Summary

We are now hiring aQC Analytical LabSupervisorto join our team inAbbvie 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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Employment Type :

Full-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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Employment Type :

Full-time

Key Skills

Laboratory Experience
Quality Assurance
FDA Regulations
ISO 9001
Quality Systems
Microbiology
Quality Control
cGMP
Laboratory Information Management Systems
QA/QC
HACCP
Manufacturing

Apply Now

About Company

AbbVie

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more

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