Did you know that your Internet Explorer is out of date?
To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.
 Google Chrome |
 Internet Explorer |
 Mozilla Firefox |
 Opera |
Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Print this job
Send Job Spec
Share on LinkedIn
Share on Facebook
Share on Twitter
Dublin South
Galway
Limerick
Limerick
Kilkenny
Limerick
Galway
Dublin North
Dublin
Limerick
Galway
Limerick
Dublin
Limerick
Tipperary
Cork
Limerick
Republic of Ireland
Republic of Ireland
Cork
Dublin
Limerick
Limerick
Limerick
Cork
Dublin
Limerick
Dublin
Dublin
Limerick
Wexford
Dublin
Galway
Galway
Limerick
Dublin
Cork
Dublin South
Dublin Greater
Dublin
Cork
Galway
Dublin South
Republic of Ireland
Dublin
Wexford
Dublin
Dublin
Dublin
Dublin
Dublin
Limerick
Netherlands
Limerick
Dublin
Galway
Limerick
Dublin
Limerick
Galway
Dublin North
Limerick
Dublin
Limerick
Galway
Dublin
Louth
Galway
Galway City
Dublin
Dublin
QC Associate Manager (LO A007956)
| Reference: | A007956 | Location: |
Limerick |
| Qualification: | Degree | Experience: | 5-7 Years |
| Job Type: | Permanent | Salary: | Not Disclosed |
Summary:Oversees the laboratory quality control testing of in-process, stability, and final drug products. Has technical responsibility for all bioanalytical aspects of QC testing.
Essential Duties and Responsibilities include, but are not limited to, the following:
• Coordinates with members of Manufacturing, Stability, and Business Ops to provide analytical support.
• Manages QC Analysts, distributes work load, and monitors progress.
• Manages product testing to ensure efficient and compliant operations.
• Reviews test reports.
• Ensures QC Analysts receive proper training.
• Attends meetings to keep informed of manufacturing priorities.
• Ensures that safety standards are maintained.
• Ensures compliance with applicable cGMP regulations and SOPs.
• Investigates atypical and OOS test results as necessary.
• Manage assay transfer internally from R&D to the QC laboratory or from PAS to the QC Laboratory.
• Manage assay transfer externally from QC laboratory to contract labs, includes audits if needed.
• Manages QC projects including analytical commitments for Regulatory filing, follow-up actions for general GMP inspections and its readiness.
• Track and coordinate major analytical investigation
• Track and monitor timeline of analytical validation projects.
• Monitor the team performance for Compliance events, track, assist and organize continuous improvement events.
• Interact with Regulatory Agencies as needed to ensure cGMP compliance.
• Special projects as assigned.
• Performs personnel management functions including time sheet submissions, scheduling of vacations, personnel development/feedback, and performance evaluations
Education and Experience:
• Requires BS/BA in Life Sciences or related field with 6+ years of relevant experience, preferably in the pharmaceutical or biotechnology industry. Previous supervisory/ leadership experience in a laboratory environment is required.
Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2020 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
Valid XHTML - CSS
