Manager, Quality Control

PowerToFly

Sligo Municipal Borough District

On-site

EUR 50,000 - 70,000

Full time

14 days+
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Job summary

PowerToFly is seeking a QC Manager to join its team at the Manorhamilton Road site in Sligo. This role is crucial for managing a lab team responsible for quality control testing and ensuring compliance with safety and product specifications.

The ideal candidate will hold an M.Sc./B.Sc. in Chemistry, with at least 4 years of people management experience in a pharmaceutical lab setting. Responsibilities include overseeing lab operations and analytical testing for API and OSD products.

Qualifications

  • Minimum 4 years of experience in people management within a pharmaceutical lab setting.
  • Strong knowledge of QA/QC operations.
  • Excellent presentation skills.

Responsibilities

  • Manage a lab team performing QC testing, ensuring compliance with regulations.
  • Conduct supervisory aspects of API and OSD analytical testing.
  • Prepare and present technical reports to stakeholders.

Skills

People management
Analytical testing for API and OSD
Quality assurance and compliance
Technical report writing
Communication skills

Education

M.Sc./B.Sc. in Chemistry or a related discipline

Job description

We are looking for a QC Manager to join our team on the Manorhamilton Road site in Sligo. The QC Lab Manager is integral to managing a team responsible for QC testing, ensuring adherence to product specifications, quality, and safety goals. This role involves overseeing laboratory operations, including analytical testing for API and OSD products, and coordinating with internal teams to meet testing schedules.

Responsibilities
  • Manage a lab team performing QC testing, ensuring compliance with data integrity policies and regulatory requirements.
  • Conduct and supervise all aspects of API and OSD analytical testing.
  • Ensure timely sampling, inspection, and testing, coordinating with teams for schedules and priorities.
  • Participate in internal and external audits and address audit findings.
  • Prepare technical reports, lead investigations, and implement CAPAs.
  • Provide training and support to lab team to achieve daily and long-term goals.
  • Present technical data to stakeholders to facilitate prompt decision‑making.
  • Report to the Senior QC Manager.
Qualifications
  • M.Sc./B.Sc. in Chemistry or a related discipline.
  • Minimum 4 years of experience in people management within a pharmaceutical lab setting.
  • Strong knowledge of QA/QC operations, analytical testing for API and OSD.
  • Excellent presentation and technical report writing skills.
  • Strong communication and interpersonal skills, with a commitment to quality and compliance.
Equal Opportunity Employer

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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