Shop Floor QA: GMP Label & Batch Review Lead

Panda International; Geleen; On-site; EUR 52,000 - 76,000; Full time

Job summary

Panda International is seeking a detail-oriented QA Officer to join the shop floor quality team on-site in the Netherlands. You will be the go-to person for GMP label control and batch documentation review to ensure production stays compliant and on schedule.

Responsibilities include label issuance and reconciliation, batch record review (aseptic/APS experience preferred), and on-floor QA support. Strong communication across Manufacturing, Warehouse, and Quality Systems is essential.

Qualifications

• Bachelor’s degree in Life Sciences, Pharmacy, Chemistry or related field.
• 1–3+ years in QA or quality-focused production in GMP pharma/biotech environment.
• Hands-on batch record review experience, ideally including aseptic processing or APS.
• Solid knowledge of GMP and Good Documentation Practices (ALCOA+).
• Experience with label control or materials reconciliation is a strong plus.
• Detail-oriented with comfort working on the shop floor.
• Fluent English; Dutch is a plus.

Responsibilities

• Label control (approx. 50-60%): issue, control and reconcile GMP labels against documentation and schedules.
• Batch record review (approx. 30-40%): review batch records for accuracy and GMP compliance; support batch disposition.
• Shop floor QA support (approx. 10-20%): monitor GMP, document deviations, escalate issues and support investigations.
• Collaborate with Manufacturing, Warehouse and Quality Systems to resolve documentation issues.
• Support inspections, audits and regulatory commitments related to documentation and label control.

Skills

Detail-oriented

Strong communication

Fluent English

Quality mindset

Education

Bachelor’s degree in Life Sciences / Pharmacy / Chemistry or related field

Job description

Panda International is seeking a detail-oriented QA Officer to join the shop floor quality team on-site in the Netherlands. You will be the go-to person for GMP label control and batch documentation review to ensure production stays compliant and on schedule.

Responsibilities include label issuance and reconciliation, batch record review (aseptic/APS experience preferred), and on-floor QA support. Strong communication across Manufacturing, Warehouse, and Quality Systems is essential.