Packaging Analyst Project
Packaging Analyst Project
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Job Description
AbbVie helps people around the world live better days and better lives each year.
And that takes all of us.
We are now recruiting a Packaging Analyst Visual Inspection to join our diverse Core 1 New Product Introduction team in AbbVie Westport on an initial 12 months fixed term contract.
As part of the new product introduction team reporting to the Manufacturing Supervisor in this role you will complete initial and investigation tasks working with QA and Operations for investigation and implement robust actions to prevent future Non Conformances implement these actions from operations perspective.
You will be responsible for creating and updating Visual Inspection strategy documents and inspection procedures for New Product Introduction.
So lets tell you a little more about this role
Key activities you will perform in the role:
- Provide guidance to department to ensure all complaints are fully investigated and suitable CAPA implemented. Liaise with corporate QA and other departments as part of the case investigation
- Liaise with internal departments QA and departments to achieve closure of complaint cases in a timely manner.
- Manage the opening tracking and maintain records for complaints received and any CAPAS opened as a result of investigations.
- SOP updates Completing all SOP updates required for Inspection departments.
- Data Integrity Completing all electronic and logbook audit trails for V&I department completing biannual checks for system users (BECSV010 forms match the actual users and levels on systems) and populating the required paperwork for checks completed adding and removing users as requested by BECSV010 forms ensuring the safe and legible storage for BECSV010 forms for each system. Updating Risk Assessments on any system updates.
- Inspection Qualifications with Inspection Personnel Performing annual qualifications with new personnel and requalifications with existing personnel from V&I dept.
- Defect management liaising with QCI on the creation and maintenance of defect sets for the different container closure systems
Qualifications :
The educational background and preferred experience we look for:
- Leaving Certificate or equivalent
- Minimum of 2 years experience working in the pharmaceutical industry
- Good Documentation Practices in a GMP environment
- Previous experience in the use of Trackwise and Document management systems would be desirable
- Proficient computer skills including: Word Excel.
- Excellent written and communication skills
- Highly motivated and a self starter
- Ability to multitask numerous complaints
- Good interpersonal skills
- Good time management and organizational skills
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:
No
Employment Type :
Fulltime
Employment Type
Full-time
