Sponsorship verdict
No sponsorship evidence yet
No government record and no wording either way. Not a refusal: ask the recruiter.
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No government sponsor record hereNo government sponsor record covers this employer in this country.
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The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
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Can’t check pay against the visa rulesNo salary stated. Ireland Critical Skills Employment Permit needs at least €40,904 a year (General Employment Permit: €36,605).
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✓
Confirmed live todayWhen a source last listed this job as open.
Details and sources
- Can’t check pay against the visa rules
- No salary stated. Ireland Critical Skills Employment Permit needs at least €40,904 a year (General Employment Permit: €36,605). Source: https://enterprise.gov.ie/en/what-we-do/workplace-and-skills/employment-permits/permit-types/critical-skills-employment-permit/, rules effective 2026-03-01.
A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.
Before you apply
Sponsorship unknown
No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.
These come from the posting’s own wording. Read the original listing to confirm. See better-fit alternatives →
About the role
• Perform a range of microbiological testing activities to support product release and site compliance, including:
• Environmental Monitoring (EM)
• Water Sampling
• Bioburden Testing
• Endotoxin Testing
• Growth Promotion Testing
• In-Process Testing
• Sterility Testing
• Antimicrobial Preservative Effectiveness Testing (APET)
• Antibiotic Assays
• Generate accurate and timely technical reports and test documentation.
• Draft, review, and maintain quality documentation, including:
• Standard Operating Procedures (SOPs)
• Protocols
• Training Materials
• Investigation Reports
• Corrective and Preventive Actions (CAPAs)
• Deviations
• Trend and analyse microbiological data, investigating adverse, atypical, and out-of-specification (OOS) results as required.
• Support validation and qualification activities for microbiology laboratory equipment and test methods.
• Ensure all testing activities are performed in compliance with cGMP, regulatory requirements, and site quality standards.
• Third-level qualification in Microbiology , Biological Sciences , or a related scientific discipline.
• Minimum of 12 months' experience within a regulated manufacturing environment, preferably in aseptic pharmaceutical production .
• Strong working knowledge of the pharmaceutical industry , including sterile manufacturing processes and GMP requirements.
• Practical experience in aseptic processing , contamination control, and microbiological laboratory techniques.
• Demonstrated understanding of microbiological testing methods, environmental monitoring, and sterile operations.
• Strong technical, analytical, and problem-solving skills, with the ability to investigate and resolve microbiological issues.
• Experience working within a highly regulated environment, with a commitment to quality, compliance, and continuous improvement.
• Excellent communication, documentation, and report-writing skills.
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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