QA Specialist
Pfizer
full-time
Posted on:
Location Type: Office
Location: Dublin • 🇮🇪 Ireland
Visit company websiteJob Level
JuniorMid-Level
About the role
- Evaluate and review Pfizer’s clinical and commercial batches of drugs
- Ensure product and process documents match specifications
- Identify deviations from established standards
- Approve investigations and change control activities
- Complete walkthrough audits to ensure cGMP compliance
- Review and approve validation documents and master batch records
- Report batch deviations in accordance with corporate standards
- Assist in the creation and maintenance of QA policies and SOPs
- Support new product introduction and continuous improvement projects
Requirements
- Relevant Third Level Qualification or Equivalent
- Minimum 2 years experience in a QA/QC GMP environment in a Pharma/Biotech company
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team in a fast-paced environment
- Proactive approach and strong critical thinking skills
Benefits
- Health insurance
- 401(k) matching
- Flexible working hours
- Paid time off
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
cGMP complianceQA policiesSOPsvalidation documentsmaster batch recordsdeviation reportingchange control activitieswalkthrough auditscontinuous improvementnew product introduction
Soft skills
communication skillsinterpersonal skillsindependent workteam collaborationproactive approachcritical thinking
Certifications
Relevant Third Level Qualification