Manufacturing Analyst
Manufacturing Analyst
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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 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 worklife 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 nonconformance 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 cordination 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.
Qualifications :
So what do you need to do this role
Education and preferred experience:
- Bachelors 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
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
