GMP QA Specialist: Packaging & Labeling — 3-Shift

SIRE LIFE SCIENCES; Breda; On-site; EUR 45,000 - 60,000; Full time

Job summary

A pharmaceutical manufacturing firm in Noord-Brabant is seeking a Quality Assurance Specialist for the Plant QA team. This role requires oversight during packaging and labeling, ensuring compliance with GMP standards. Responsibilities include conducting quality checks, reviewing batch records, and collaborating with production teams. Candidates should have a relevant degree and approximately 3 years of QA experience. This position involves a fixed 3-shift schedule and demands excellent attention to detail and communication skills.

Qualifications

• Approximately 3 years of QA or manufacturing experience in pharmaceuticals or medical devices.
• Strong knowledge of GMP, GDP, and/or GCP regulations.
• Fluent in English with good collaboration skills.

Responsibilities

• Conduct final quality checks on labeling and packaging processes.
• Review batch records for accuracy and compliance.
• Investigate deviations and document findings.
• Collaborate with Production and QA colleagues to address quality concerns.
• Support GMP compliance activities and review operational SOPs.

Skills

Attention to detail

Knowledge of GMP

Communication skills

Ability to work under pressure

Education

MBO or BSc in Pharmaceutical, Life Sciences

Job description

A pharmaceutical manufacturing firm in Noord-Brabant is seeking a Quality Assurance Specialist for the Plant QA team. This role requires oversight during packaging and labeling, ensuring compliance with GMP standards. Responsibilities include conducting quality checks, reviewing batch records, and collaborating with production teams. Candidates should have a relevant degree and approximately 3 years of QA experience. This position involves a fixed 3-shift schedule and demands excellent attention to detail and communication skills.