AbbVie invites you to join our cutting-edge pharmaceutical facility in Sligo nestled in a region known for its vibrant community and scenic beauty. Embrace an opportunity to grow your career while contributing to meaningful innovations that enhance global health.
An exciting role has opened up on our Ballytivnan site in Sligo. We are currently looking for a Quality Manager overseeing the Medical Device Quality team reporting to the Quality Site Head. You will oversee the whole quality function for the medical device business on site. Youll ensure compliance with quality standards and regulatory requirements leading a dedicated team of quality professionals.
Responsibilities
- Quality Assurance & Control: Oversee testing of raw materials manufacturing quality control and product validation.
- Team Leadership: Manage and lead a team responsible for compliance and quality oversight.
- Regulatory Compliance: Ensure adherence to corporate and regulatory requirements.
- Performance Reporting: Report on the performance of the quality management system to senior management.
- Issue Resolution: Timely resolution of quality issues and acting as a site representative during regulatory inspections.
- Budget Management: Assist in the development and administration of the quality departments annual budget.
Qualifications :
- Essential: Bachelors degree in science/engineering and 5 years experience in the healthcare/pharmaceutical industry.
- Desired: Masters degree preferred.
- Experience: 6 years in Manufacturing/QA/R&D in relevant industries and 3 years in quality management.
- Skills: Familiarity with statistical quality systems cGMP and regulatory requirements. Strong leadership communication and interpersonal skills are necessary.
- Attributes: High attention to detail commitment to quality and integrity.
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 invites you to join our cutting-edge pharmaceutical facility in Sligo nestled in a region known for its vibrant community and scenic beauty. Embrace an opportunity to grow your career while contributing to meaningful innovations that enhance global health. An exciting role has opened up on ou...
AbbVie invites you to join our cutting-edge pharmaceutical facility in Sligo nestled in a region known for its vibrant community and scenic beauty. Embrace an opportunity to grow your career while contributing to meaningful innovations that enhance global health.
An exciting role has opened up on our Ballytivnan site in Sligo. We are currently looking for a Quality Manager overseeing the Medical Device Quality team reporting to the Quality Site Head. You will oversee the whole quality function for the medical device business on site. Youll ensure compliance with quality standards and regulatory requirements leading a dedicated team of quality professionals.
Responsibilities
- Quality Assurance & Control: Oversee testing of raw materials manufacturing quality control and product validation.
- Team Leadership: Manage and lead a team responsible for compliance and quality oversight.
- Regulatory Compliance: Ensure adherence to corporate and regulatory requirements.
- Performance Reporting: Report on the performance of the quality management system to senior management.
- Issue Resolution: Timely resolution of quality issues and acting as a site representative during regulatory inspections.
- Budget Management: Assist in the development and administration of the quality departments annual budget.
Qualifications :
- Essential: Bachelors degree in science/engineering and 5 years experience in the healthcare/pharmaceutical industry.
- Desired: Masters degree preferred.
- Experience: 6 years in Manufacturing/QA/R&D in relevant industries and 3 years in quality management.
- Skills: Familiarity with statistical quality systems cGMP and regulatory requirements. Strong leadership communication and interpersonal skills are necessary.
- Attributes: High attention to detail commitment to quality and integrity.
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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