QA Specialist – Sterile Production

About the role

The QA Specialist – Sterile ensures that all in‑process production and packaging activities for biotech and sterile products comply with current Good Manufacturing Practice (cGMP) standards. The role supports Julphar’s quality procedures, participates in audits, and drives corrective actions to maintain regulatory compliance.

Key responsibilities

• Perform in‑process quality checks according to SOPs and record results in batch records.
• Inspect incoming materials, verify specifications, and manage non‑conforming items.
• Investigate deviations, support corrective and preventive actions, and document findings.
• Participate in media fills, line clearance checks, and ensure equipment calibration.
• Enter quality data into the SAP system and assist with Annual Product Quality Review (APQR) reports.
• Maintain in‑process control documents, logbooks, and accurate QA activity records.
• Support internal and external regulatory audits.
• Plan and assign daily QA tasks to meet quality and operational goals.

Required profile

• Results‑oriented with a strong sense of accountability and ownership.

Required skills

• cGMP knowledge
• Proficiency with SAP for quality data entry

What we offer

• Opportunity to work in a leading pharmaceutical company focused on innovation and patient care.