We are seeking a highly organized and proactive Quality Control Laboratory Planner to join our Quality Laboratory team at AbbVie in Westport on a 12 month fixed-term-basis. As a QC Laboratory Planner you will be responsible for the planning and control of the testing schedule for all Westport manufactured products. This role involves preparing both short-term and long-term testing schedules incorporating non-routine testing needs such as process validation customer complaints and non-conformance testing.
Key Responsibilities:
- Coordinate with various stakeholders including Planning Manager Supply Chain Planners Operations and QA to ensure timely testing and release of results.
- Develop and maintain short-term and long-term testing schedules collaborating with the QC team and site stakeholders.
- Host and chair the weekly QC Release meeting and issue weekly QC testing schedules to stakeholders.
- Work closely with QC Supervisors to develop training matrices ensuring optimal coverage cross-training and resource capacity in the QC laboratory.
- Ensure instrumentation availability and utilization in support of testing schedules.
- Analyze data for improvements in workflow testing capabilities and efficiencies reporting laboratory performance metrics regularly.
- Serve as the key contact within the QC department for updates on testing status and schedule changes.
- Perform additional duties as directed by QC Managers and Senior Management.
Qualifications :
- Bachelors degree or above in Chemistry a related science or a planning and scheduling discipline.
- Minimum of 3-5 years of related pharmaceutical experience (QC Manufacturing Supply Chain QA etc).
- Experience in planning or scheduling within a QC laboratory environment is advantageous.
- Proficiency in Microsoft Office Suite and understanding of Lean Manufacturing concepts.
- Strong time management organizational and project management skills.
- Excellent communication skills with the ability to build and develop strong cross-functional relationships.
- Ability to positively influence a wide range of stakeholders to achieve optimal testing schedules.
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 :
No
Employment Type :
Full-time
We are seeking a highly organized and proactive Quality Control Laboratory Planner to join our Quality Laboratory team at AbbVie in Westport on a 12 month fixed-term-basis. As a QC Laboratory Planner you will be responsible for the planning and control of the testing schedule for all Westport manufa...
We are seeking a highly organized and proactive Quality Control Laboratory Planner to join our Quality Laboratory team at AbbVie in Westport on a 12 month fixed-term-basis. As a QC Laboratory Planner you will be responsible for the planning and control of the testing schedule for all Westport manufactured products. This role involves preparing both short-term and long-term testing schedules incorporating non-routine testing needs such as process validation customer complaints and non-conformance testing.
Key Responsibilities:
- Coordinate with various stakeholders including Planning Manager Supply Chain Planners Operations and QA to ensure timely testing and release of results.
- Develop and maintain short-term and long-term testing schedules collaborating with the QC team and site stakeholders.
- Host and chair the weekly QC Release meeting and issue weekly QC testing schedules to stakeholders.
- Work closely with QC Supervisors to develop training matrices ensuring optimal coverage cross-training and resource capacity in the QC laboratory.
- Ensure instrumentation availability and utilization in support of testing schedules.
- Analyze data for improvements in workflow testing capabilities and efficiencies reporting laboratory performance metrics regularly.
- Serve as the key contact within the QC department for updates on testing status and schedule changes.
- Perform additional duties as directed by QC Managers and Senior Management.
Qualifications :
- Bachelors degree or above in Chemistry a related science or a planning and scheduling discipline.
- Minimum of 3-5 years of related pharmaceutical experience (QC Manufacturing Supply Chain QA etc).
- Experience in planning or scheduling within a QC laboratory environment is advantageous.
- Proficiency in Microsoft Office Suite and understanding of Lean Manufacturing concepts.
- Strong time management organizational and project management skills.
- Excellent communication skills with the ability to build and develop strong cross-functional relationships.
- Ability to positively influence a wide range of stakeholders to achieve optimal testing schedules.
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 :
No
Employment Type :
Full-time
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