Quality Control Specialist

About the role

The Quality Control Specialist will join the Quality team to support daily QC operations across raw materials, in‑process materials and finished goods. You will ensure accurate record‑keeping, perform inspections, and contribute to investigations of non‑conforming products.

Key responsibilities

• Perform routine QC testing of incoming raw materials, in‑process materials and finished products.
• Plan and schedule daily QC runs, both routine and ad‑hoc, as assigned.
• Evaluate test data, generate reports and highlight deviations from SOPs.
• Raise non‑conformances and support root‑cause investigations.
• Draft and revise QC work instructions and assist with validation and stability studies.
• Maintain laboratory housekeeping, equipment upkeep, document archival and reagent inventory.
• Apply Good Documentation Practices to ensure traceability and audit readiness.

Required profile

• Degree or diploma in Biomedical Science, Biotechnology, Molecular Biology, Biochemistry or related life‑science field.
• 2‑3 years of QC experience, preferably in medical‑device manufacturing.
• Ability to work independently and collaboratively with cross‑functional teams.
• Strong organizational, time‑management and communication skills.

Required skills

• Hands‑on experience with qPCR equipment.
• Proficiency using standard laboratory tools such as pipettes and centrifuges.
• Basic computer competency, especially Microsoft Office applications.
• Knowledge of Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP).