Manufacturing Analyst

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 www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

AbbVie helps people around the world live better days and better lives each year. And that takes all of us.

We are now recruiting for a Manufacturing Analyst to join our newly formed Central Cervices Team  in AbbVie Westport, Co Mayo on an initial 12 months fixed term contract.

Established in 1977, AbbVie Westport is a Centre of Excellence for Aseptic for Commercial manufacturing of Biologics & Eyecare (pharmaceutical) products. In the role, you will have the opportunity to coordinate batch record flow, corrections, manufacturing status tracking spreadsheets, report preparation, Complaints tracking. The successful candidate will perform reviews of manufacturing and other paperwork to ensure compliance to Abbvie and regulatory standards. The manufacturing analyst will be required to communicate up to date status reviews and work with Manufacturing Technicians, Technical Writers and Technical Shift leads to coordinate and ensure the completion of manufacturing batch paperwork.

If great benefits, a defined career path, and work-life balance are important in your next career move, then read on to find out more:

Key activities:

• Compile and perform manufacturing audit review of batch paperwork from manufacturing areas.
• Ensure all batch records components are present and that all corrections identified during initial review and by Product Release Team are addressed in a timely and compliant manner.
• Use and maintenance of data within key systems such as SAP, S4HANA.
• Document retrieval from local files and archives, as required for submissions, customer requests and others.
• Participate in non-conformance and exception investigations as necessary.
• Work with QA Teams to align and promote awareness on data integrity and good documentation practices.
• Facilitate and coordinate with project teams to enhance, improve and streamline batch records.
• Management of purchasing requisitions.
• Provide assistance when required at Regulatory Inspections.
• Trending and c-ordination of customer complaints investigations.
• Work close with Departments on corrective actions arising from Environmental excursions.
• Comply with AbbVie policies and procedures and regulatory agency regulations.

So, what do you need to do this role?

Education and preferred experience:

• Bachelor’s degree in science, or a related field is preferred and/or a minimum of 2 years’ experience in a similar role.
• Detailed knowledge of CGMP and aseptic practices, data integrity requirements and GDP is required for this role.
• Strong organizational skills and attention to detail are essential for this role.
• Good interpersonal relations/communications skills

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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

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