Quality Control Senior Associate (Biopharmaceutical QC)

Location: Dublin, Ireland

Salary: €52,756.95–€71,377.05 per year

Company

hirify.global is a biopharmaceutical organization.

What you will do

• Plan and perform complex routine and non-routine analytical methods and a broad range of assays.
• Test commercial products, stability samples, utilities, raw materials, and validation samples.
• Report, evaluate, trend, approve, and archive analytical data, including LIMS coordination for commercial and import testing.
• Troubleshoot laboratory issues, conduct investigations, and communicate solutions to stakeholders.
• Review protocols and perform assay validation, equipment qualification, method transfers, and verification activities.
• Support audits, regulatory filings, controlled-document changes, laboratory compliance, and team projects; train others when required.

Requirements

• Bachelor’s degree in a science-related field.
• 4+ years of biopharmaceutical QC, quality control, or GMP laboratory experience in the pharmaceutical or medical device industry.
• Experience with regulatory compliance in cGMP manufacturing and pharmaceutical product testing.
• Knowledge of GMP QC analytical laboratory principles, regulatory requirements, aseptic compliance, and data integrity.
• Strong technical writing, investigation, problem-solving, statistical analysis, communication, and project organization skills.
• Ability to work independently under minimal supervision, make decisions, escalate issues, and deliver right-first-time results.

Culture & Benefits

• Full-time position with potential extended-hours and weekend work as required.
• Work includes collaboration with internal stakeholders, regulatory agencies, outside resources, and cross-functional teams.
• Opportunities to contribute to departmental and organizational initiatives and to coach or train colleagues.