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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.
Job Description
Welcome to AbbVie! 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.
Key Activities
* Coordinating technical operations change control and change plan activities.
* Updating, generating, maintaining and issuing internal documentation.
* Control of validation / process validation documentation.
* Control of document change requests and changes to documented procedures.
* Act as department training coordinator and 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 Manager.
* Coordinating monthly review of Technical Operations budgets, ensuring the department is meeting its targets.
* Supporting all EHS & E standards, procedures and policies.
* Ensuring compliance with cGMP and HPRA/FDA regulations and company policies, procedures and guidelines.
Qualifications
* Third Level Qualification in a relevant discipline is required.
* Minimum of three years experience in a regulated manufacturing industry.
* Strong IT skills.
* Experience 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 to collate and control 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
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