QC Specialist – Separations: Precision Lab & Method Transfer

jj; Ireland; Hybrid; EUR 52,000 - 83,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Well-being reimbursement

Job summary

Johnson & Johnson in Ringaskiddy, Cork, Ireland, is seeking a QC Specialist – Separations to join our Quality Control team. You will provide technical support for analytical testing, equipment qualification, and method transfer in a regulated pharmaceutical setting.

The role requires hands-on knowledge of analytical techniques in Chemistry, Biochemistry, or Microbiology, with prior supervisory experience in an IMB/FDA-regulated facility. Collaboration and continuous improvement are key.

Qualifications

• Minimum of 3 years of pharmaceutical industry experience.
• Prior supervisory experience in an IMB/FDA-regulated facility.
• Knowledge of FDA and EMA regulatory requirements for biologics/pharma.
• Sound knowledge of analytical techniques and laboratory equipment.

Responsibilities

• Support day-to-day testing operations.
• Coordinate qualification of analytical equipment and testing functions (HPLC, spectrophotometry, nephelometry, TOC).
• Coordinate sampling during plant and laboratory utility qualification.
• Plan and coordinate analytical method transfer for NMEs.
• Coordinate testing for raw materials, in-process samples, products.
• Assist implementation of analyst training programs.
• Review laboratory data, deviations, CAPAs, and change controls.
• Present analytical information to regulatory inspectors and stakeholders.

Skills

Collaboration and teamwork

Critical thinking

Problem-solving

Attention to detail

Results-oriented

Coaching and mentoring

Integrity and accountability

Clear communication

Adaptability

Innovative mindset

Inclusive collaboration

Tools

HPLC

Spectrophotometry

Nephelometry

TOC systems

Job description

Johnson & Johnson in Ringaskiddy, Cork, Ireland, is seeking a QC Specialist – Separations to join our Quality Control team. You will provide technical support for analytical testing, equipment qualification, and method transfer in a regulated pharmaceutical setting.

The role requires hands-on knowledge of analytical techniques in Chemistry, Biochemistry, or Microbiology, with prior supervisory experience in an IMB/FDA-regulated facility. Collaboration and continuous improvement are key.