Job Description If you want to be a difference maker our people are waiting.
See the difference you can make at AbbVie.
We are now recruiting a Packaging Analyst to join our high-performing Central Services Team in Westport , Co. Mayo on a fixed-term contract.
In this role, you will conduct investigations through Global Trackwise, (CAPAs / SCARs.
), update SOPs, Work Instructions and perform periodic reviews on One Vault.
You will also carry out training with Operators on changes made to SOPs, highlighting where the changes will impact the operator's role in the day to day tasks in which they perform.
You will be responsible for investigating complaints that return to site, attending meetings and reporting findings from investigations.
So let's tell you a little more about this role… Key Activities: CAPA / Non Conformances – initiating and documenting investigations, completing root cause analysis, technical writing of investigation reports.
Change Control – initiating and documenting change controls through Global Trackwise for any changes deemed necessary in the Packaging Departments.
Ownership and completion of associated change actions.
OneVault – generating, updating and management of procedure and work instruction documents.
Submitting of change requests for procedure/WI updates.
Creating and revising procedures by analyzing current practices and / or improvements.
Complaints – investigation of complaints received associated with Packaging processes.
Actively participate in the training of employees as deemed required.
Creation and updating of the system risk assessments, where required.
Presenting of Packaging Department subjects, specific to CAPA and CC, in regulatory and internal audits.
Attend CAPA Investigation meetings with internal stakeholders, Global Packaging and suppliers.
Qualifications So, what do you need to excel in this role: Qualifications; Education, Competencies and Experience Third level qualification in a relevant discipline is preferred and/or 3+ years experience working in a similar role.
Knowledge of regulatory requirements in a pharmaceutical GxP environment.
Preferred Experience: S4 HANA, One Vault, Global Trackwise, Microsoft Office (Word, Excel, PowerPoint etc.).
Experience of working on a team, including strong organizational and time management skills.
Ability to learn new and different technologies.
Ability to effectively communicate plans, proposals, and actions at management levels.
Excellent Communication and presentation skills, both written and verbal.
Ability to identify and understand issues, problems and opportunities whilst providing a viable solution.
Proven to be self-directed, self-motivated and ability to prioritise competing priorities So, does this sound like the opportunity you have been looking for?
Then join AbbVie!
Additional Information AbbVie is an equal opportunity employer and 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.
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
