QC Specialist, Separations: Lead Analytical Testing

7566-Janssen Sciences Ireland Unlimited Company Legal Entity; Barnahely; On-site; EUR 52,000 - 83,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Bereavement leave

Caregiver leave

Volunteer leave

Well-being reimbursement

Insurance plans

Job summary

Johnson & Johnson seeks a QC Specialist – Separations to join our Quality Control team in Ringaskiddy, Cork, Ireland. You will provide technical expertise and support for analytical testing, equipment qualification, method transfer activities, investigations, and continuous improvement initiatives in a GMP environment.

The role requires sound knowledge of analytical techniques and laboratory equipment in Chemistry, Biochemistry, or Microbiology, with prior supervisory experience in an

Qualifications

• Experience minimum of 3 years in the pharmaceutical industry.
• Prior supervisory experience in an IMB/FDA-regulated facility.
• Knowledge of FDA and EMA regulatory requirements applicable to biologics/pharmaceuticals.
• Technical knowledge of analytical techniques and laboratory equipment in Chemistry, Biochemistry, and/or Microbiology.
• Strong collaboration, critical thinking, and communication skills.

Responsibilities

• Support day-to-day testing operations in QC.
• Coordinate qualification of analytical equipment and testing functions (HPLC, Spectrophotometry, Nephelometry, TOC).
• Coordinate sampling and testing during plant and lab utility qualification.
• Plan and coordinate analytical method transfer activities for NMEs.
• Coordinate testing for raw materials, in-process samples, final bulk and finished products.
• Review data, investigations, deviations, CAPAs, and Change Controls.

Skills

Analytical Techniques

Team Collaboration

Problem Solving

Detail Orientation

Regulatory Knowledge

Job description

Johnson & Johnson seeks a QC Specialist – Separations to join our Quality Control team in Ringaskiddy, Cork, Ireland. You will provide technical expertise and support for analytical testing, equipment qualification, method transfer activities, investigations, and continuous improvement initiatives in a GMP environment.

The role requires sound knowledge of analytical techniques and laboratory equipment in Chemistry, Biochemistry, or Microbiology, with prior supervisory experience in an