Company 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

Welcome to AbbVie!

What you do, is what we need. Making a difference begins here. And takes all of us.

We are now recruiting for a Technical Operations Co-Ordinator to join our Technical Operations team in AbbVie Sligo on a fixed term, 12 month contract. In this role you will coordinate technical operations change management, manage training requirements for the team, coordinate document control, and budget control for the technical operations area in addition to providing support to ensure plant technical, quality and safety goals are met. You will also have an opportunity to participate in continuous improvement projects as assigned by the Technical Operations Manager.

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 you will perform in the role:

 

Coordinating technical operations change control and change plan activities.Updating, generation, maintenance and issuing of internal documentation.Control of validation / process validation documentation.Control of document change requests and changes to documented procedures.Act as department training coordinator and to work with the site Training coordinator with respect to department activities for training plans, curriculum and training assignments.Leading Operational Excellence quality projects on site assigned by the Technical Operations ManagerCoordinating monthly review of Technical Operations budgets. Ensuring the department is meeting its targets.While adhering to and supporting all EHS & E standards, procedures and policies.Also adherering to and following all procedures policies and guidelines ensuring compliance with cGMP and HPRA/FDA regulations and company policies, procedures and guidelines.
Qualifications

The educational background and preferred experience we look for:

Third Level Qualification in a relevant discipline is required.A minimum of three years experience in a regulated manufacturing industry.Strong IT skillsExperience in an HPRA/FDA regulated industry is desirable but not essential.Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry.Proven track record of project planning / maintenance planning.Ability of collating and controlling technical documentation developed on site.
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.html