Supervisor, Laboratory Quality Control at AbbVie AS


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 . Follow @abbvie on , , , and .
Job Description
We are now looking for a QC Supervisor to join our team in Clonshaugh, Dublin. As a QC Supervisor, you will be responsible for the QC tech transfer team, monitoring and directing the day-to-day activities in the QC laboratory, including adherence to the System for Management. You will work cross functionally with local and global teams to ensure the successful transfer of products to our site and QC lab.
As QC Supervisor, you will be required to adhere to and enforce all applicable laws and regulations as well as internal Company policies and procedures in the performance of the job role. This position supervises a team of QC Chemists and reports to the QC Manager.
  • Establish the expectation and standards, and the supportive environment, to ensure that staff has the capability to meet performance expectations. This includes building staff capability by providing ongoing coaching and mentoring of direct reports, providing timely recognition as well as performance counseling, building and executing development plans, and providing career counseling for career progression.
  • Supervise daily laboratory operations, ensuring laboratory personnel execute their responsibilities in strict accordance with relevant regulatory guidelines.
  • Support the weekly and daily production schedules and participate in the daily Tier 0 meetings to review shift production goals and to review execution against the shift’s goals.
  • Attend with the supervisors of support functions daily Tier 1 meetings to review shift production goals and execution against the shift’s goals.
  • Provide direction to laboratory personnel internally and at contract laboratories to ensure production is able to complete the targets specified in the daily production plan.
  • Manage samples for analytical testing and the generation of results at external /contract laboratories
  • Ensure proper coverage in the laboratory by trained, skilled chemists.
  • Ensure that laboratory personnel properly follow procedures and submit required documentation completely, accurately and timely according to current cGMPs.
  • Ensure data reports on own team’s performance are current, accurate, and distributed according to defined procedures.
  • Maintain metrics for laboratory calibration, maintenance and utilization of instrumentation and equipment.
  • Contribute to the continual improvement of all laboratory documentation to ensure they are current, accurate, and clearly define process and role responsibilities.
  • Schedule and/or deliver training to laboratory personnel to ensure staff has the requisite skills to perform their work correctly, safely, and compliantly.
  • Maintain accountability for own team’s performance metrics that support the annual operating plan and site strategic plan objectives.
  • Seek process innovation and continuous process improvement in laboratory area.
  • Provide timely status reports to laboratory management on the status and effectiveness of the laboratory Installation, Qualification, calibration and maintenance programs.

Qualifications
  • Minimum of 4 years relevant Quality Control experience.
  • Good understanding of pharmaceutical manufacturing operations
  • Minimum two years direct supervisory experience or demonstration of staff mentoring.
  • Experienced in aligning individuals and teams to business objectives
  • Experience in managing by metrics
  • Demonstrate strong analytical laboratory skills in a variety of applications and the ability to troubleshoot for investigative purposes.

Additional Information
AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
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 . Follow @abbvie on , , , and .
Job Description
We are now looking for a QC Supervisor to join our team in Clonshaugh, Dublin. As a QC Supervisor, you will be responsible for the QC tech transfer team, monitoring and directing the day-to-day activities in the QC laboratory, including adherence to the System for Management. You will work cross functionally with local and global teams to ensure the successful transfer of products to our site and QC lab.
As QC Supervisor, you will be required to adhere to and enforce all applicable laws and regulations as well as internal Company policies and procedures in the performance of the job role. This position supervises a team of QC Chemists and reports to the QC Manager.
  • Establish the expectation and standards, and the supportive environment, to ensure that staff has the capability to meet performance expectations. This includes building staff capability by providing ongoing coaching and mentoring of direct reports, providing timely recognition as well as performance counseling, building and executing development plans, and providing career counseling for career progression.
  • Supervise daily laboratory operations, ensuring laboratory personnel execute their responsibilities in strict accordance with relevant regulatory guidelines.
  • Support the weekly and daily production schedules and participate in the daily Tier 0 meetings to review shift production goals and to review execution against the shift’s goals.
  • Attend with the supervisors of support functions daily Tier 1 meetings to review shift production goals and execution against the shift’s goals.
  • Provide direction to laboratory personnel internally and at contract laboratories to ensure production is able to complete the targets specified in the daily production plan.
  • Manage samples for analytical testing and the generation of results at external /contract laboratories
  • Ensure proper coverage in the laboratory by trained, skilled chemists.
  • Ensure that laboratory personnel properly follow procedures and submit required documentation completely, accurately and timely according to current cGMPs.
  • Ensure data reports on own team’s performance are current, accurate, and distributed according to defined procedures.
  • Maintain metrics for laboratory calibration, maintenance and utilization of instrumentation and equipment.
  • Contribute to the continual improvement of all laboratory documentation to ensure they are current, accurate, and clearly define process and role responsibilities.
  • Schedule and/or deliver training to laboratory personnel to ensure staff has the requisite skills to perform their work correctly, safely, and compliantly.
  • Maintain accountability for own team’s performance metrics that support the annual operating plan and site strategic plan objectives.
  • Seek process innovation and continuous process improvement in laboratory area.
  • Provide timely status reports to laboratory management on the status and effectiveness of the laboratory Installation, Qualification, calibration and maintenance programs.

Qualifications
  • Minimum of 4 years relevant Quality Control experience.
  • Good understanding of pharmaceutical manufacturing operations
  • Minimum two years direct supervisory experience or demonstration of staff mentoring.
  • Experienced in aligning individuals and teams to business objectives
  • Experience in managing by metrics
  • Demonstrate strong analytical laboratory skills in a variety of applications and the ability to troubleshoot for investigative purposes.

Additional Information
AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. ","datePosted":"2024-03-26T10:41:39+00:00","validThrough":"2124-03-26T10:41:39+00:00","employmentType":["Full-time"],"hiringOrganization":{"@type":"Organization","name":"AbbVie","image":"","logo":"","sameAs":"https://careers.abbvie.com","url":"https://careers.abbvie.com"},"industry":["Operations"],"jobBenefits":"","identifier":{"@type":"PropertyValue","name":"AbbVie","value":"d949b8c2-0e4f-474e-a3d3-2372117314c1"},"jobLocation":[{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Dublin, County Dublin"}}]}
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