Job Description
AbbVie Ballytivnan are looking for a Document Control Specialist to join their team. You will be coordinating the development and the maintenance of the AbbVie Biologics Document Control system in compliance with all applicable company and regulatory requirements.
What you will do:
* Manage the document management system to ensure compliance with Quality requirements and Regulations.
* Be responsible for the company Documentation issuance, control and retention ensuring compliance with all policies and procedures.
* Work closely with the global doc centre and site stakeholders in processing, reviewing and approval process of document change requests
* Assist with external audits and inspections through coordination, participation and compilation of document packages for audit.
* Comply with the EHS policy & procedures and demonstrate EHS best practices at all times.
Qualifications
What you will need:
* 3rd level qualification in a relevant discipline
* Minimum 2 years in a similar role
* Previous experience in a GMP environment (pharma would be an advantage)
* Excellent computer skills, MS office skills essential
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
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