Microbiology QC Analyst — Drive Precise Lab Data

8170-Janssen Pharmaceutical Sciences Unlimited Company Legal Entity; Wallingstown; On-site; EUR 42,000 - 68,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Bereavement leave

Well-being reimbursement

Insurance plans

Job summary

Johnson & Johnson Cork Ireland is seeking a skilled Quality Control Analyst (Microbiology) to join our GMP laboratory team in Cork. You will perform microbiology testing, ensure data integrity, and contribute to timely material release in a fast-paced environment.

Working with QA, Manufacturing and other functions, you will maintain equipment, document results, and support regulatory inspections while upholding the highest quality standards.

Qualifications

• Level 7 in a scientific/technical discipline is required.
• Experience in the lab or similar QCA role.
• Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals.

Responsibilities

• Perform testing accurately, safely and on time per approved methods.
• Support operation, calibration, maintenance and qualification of equipment.
• Document, review and report laboratory data in GMP-compliant manner.
• Support material release, sample scheduling and KPI achievement.
• Identify and escalate deviations and atypical results as required.
• Maintain training and technical competence; share knowledge within the team.
• Prepare, review and maintain QC documentation and records.
• Collaborate with QA, Manufacturing and other functions to meet priorities.
• Support internal and external audits and regulatory inspections.
• Contribute to department goals and continuous improvement activities.

Skills

Analytical Reasoning

Compliance Management

Data Analysis

Quality Control

Report Writing

ISO 9001

Job description

Johnson & Johnson Cork Ireland is seeking a skilled Quality Control Analyst (Microbiology) to join our GMP laboratory team in Cork. You will perform microbiology testing, ensure data integrity, and contribute to timely material release in a fast-paced environment.

Working with QA, Manufacturing and other functions, you will maintain equipment, document results, and support regulatory inspections while upholding the highest quality standards.