AbbVie Biologics Ballytivnan in Sligo invites applications for the Incoming Quality Assurance Supervisor role in our Quality Assurance department. Reporting to the Quality Operations Manager this position is pivotal in ensuring materials released for both marketed and investigational drug products meet stringent AbbVie standards. You will oversee the IQA process lead investigations support continuous improvement and collaborate across teams to drive quality safety and compliance.
Responsibilities
- Oversee and ensure timely compliant release of all incoming materials for manufacturing
- Manage and provide guidance on sampling requirements especially for aseptic processes
- Lead IQA-related investigations and coordinate with contract laboratories
- Review audit and author material release records specifications and SOPs
- Act as site SME for SAP inspection plans and material management; support internal and regulatory audits
- Drive process simplification and improvements
- Guide cross-functional and cost improvement initiatives championing quality in new product introductions
- Supervise up to 5 team members fostering collaboration and maintaining a high standard of work
- Promote and uphold EHS policies supporting a culture of safety excellence
Qualifications :
- Bachelors degree or above in science quality or engineering
- At least 3 years of experience in GMP-regulated quality or operations roles in pharma or biopharma industries
- Desired: Previous people supervision
- Strong regulatory knowledge attention to detail and effective problem-solving skills
- Proven cross-functional collaboration leadership ability and solid communication 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:
Work :
No
Employment Type :
Full-time
AbbVie Biologics Ballytivnan in Sligo invites applications for the Incoming Quality Assurance Supervisor role in our Quality Assurance department. Reporting to the Quality Operations Manager this position is pivotal in ensuring materials released for both marketed and investigational drug products m...
AbbVie Biologics Ballytivnan in Sligo invites applications for the Incoming Quality Assurance Supervisor role in our Quality Assurance department. Reporting to the Quality Operations Manager this position is pivotal in ensuring materials released for both marketed and investigational drug products meet stringent AbbVie standards. You will oversee the IQA process lead investigations support continuous improvement and collaborate across teams to drive quality safety and compliance.
Responsibilities
- Oversee and ensure timely compliant release of all incoming materials for manufacturing
- Manage and provide guidance on sampling requirements especially for aseptic processes
- Lead IQA-related investigations and coordinate with contract laboratories
- Review audit and author material release records specifications and SOPs
- Act as site SME for SAP inspection plans and material management; support internal and regulatory audits
- Drive process simplification and improvements
- Guide cross-functional and cost improvement initiatives championing quality in new product introductions
- Supervise up to 5 team members fostering collaboration and maintaining a high standard of work
- Promote and uphold EHS policies supporting a culture of safety excellence
Qualifications :
- Bachelors degree or above in science quality or engineering
- At least 3 years of experience in GMP-regulated quality or operations roles in pharma or biopharma industries
- Desired: Previous people supervision
- Strong regulatory knowledge attention to detail and effective problem-solving skills
- Proven cross-functional collaboration leadership ability and solid communication 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:
Work :
No
Employment Type :
Full-time
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