Description

ICompany Description

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.

Job Description

We are looking for a Senior Manufacturing Analyst for our site in Westport, in our core 2 and core 3 parts of our facility, this will be a shift position rotation 24/7.

You will provide support to the Manufacturing Technicians and Manufacturing Analysts in achieving the overall business goals and objectives for the site.

As part of the role, you will be responsible for the day to day running of the shift - from the shift handover from the previous shift to the handover to the next shift by delegating the tasks accordingly.

As issues arise on shift they are to be communicated by the Manufacturing Technicians and Analysts to the Senior Manufacturing Analyst, who in turn escalates them to the Technical Shift Lead as required. They are then responsible for re-arranging and re-assigning shift schedule / tasks / indirect reports as issues arise.

Responsibilities:

• Ensure that all areas of responsibility are fully staffed and that any constraints are managed appropriately or escalated to the Manufacturing Manager.

• Ensure all activities are completed in line with regulatory (QA and EHS) and corporate requirements.

• Manage product improvement changes and implementation process improvements

• Lead and support Continuous Improvement initiatives as required to support the overall goals of the Manufacturing Department

• Develop, implement and maintain operational excellence methods of working within the manufacturing team in conjunction with the shift manager

• Ensure all activities of the Manufacturing Department are performed in accordance with compliance requirements, GMP, OPEX standards and relevant SOPs and policies through Process Confirmation where appropriate.

• Provide leadership at the tiered OPEX meetings to ensure focus and traction is maintained on the key objectives

• Co-ordination with maintenance department, validations and water engineers as issues arise to ensure that they are investigated and addressed in a timely manner

• Liaise with packaging and warehouse personnel in resolving SAP batch / component related issues in a timely manner

• Support and ensure QMS is maintained to a high standard

• Ensure shift updates and issues are communicated, highlight any issues with schedule adherence

• Ensure team members are cross trained, and training is progressed in a timely manner. Actively participate in the training and certification of new employees.

Qualifications

• Bachelor's Degree in a pharmaceutical science/ engineering / operations discipline.
• Minimum of 3 years relevant experience in Pharma/Medical Devices/Food Operations
• Clear understanding of working within a regulated environment

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 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.htmlI