Quality Assurance Specialist
Quality Assurance Specialist
Quality Assurance Specialist
Quality Assurance Specialist
Sire Search
Personaldienstleistungen und -beratung
Limburg an der Lahn
- Art der Anstellung: Vollzeit
- 43.500 € – 52.500 € (von XING geschätzt)
- Vor Ort
- Zu den Ersten gehören
Quality Assurance Specialist
Über diesen Job
Location: Limburg, Herten  | Sector: Chemicals | Start Date: 8/21/2025 | Job ref: 55865
The Company
A leading chemical manufacturer located in Herten, the Netherlands. The site specializes in producing high-grade hydrogen peroxide and related catalysts for use in healthcare, industrial disinfection, and other critical applications. Operating under strict GMP and ISO standards, the organization is expanding its quality assurance team to support its growing GMP operations
About the Role
As a Quality Assurance Specialist, you will be responsible for ensuring GMP compliance across production processes, documentation, and product release. You’ll work closely with operators, production managers, and the QA Manager to uphold quality standards and support continuous improvement. This role offers growth potential, with the current QA Manager planning to hand over responsibilities within five years.
Responsibilities
- Release GMP batches of hydrogen peroxide (SG and PH grades) and associated materials.
- Review and archive batch records, perform visual inspections, and assess deviations.
- Support GMP operators with daily quality-related guidance and training.
- Maintain and improve GMP documentation systems, including SOPs, logbooks, and batch records.
- Write and review Product Quality Reviews (PQRs) and trend performance indicators.
- Participate in morning meetings to discuss production challenges and delivery timelines.
- Ensure timely communication with internal teams and customers regarding product availability.
- Work in cleanroom environments with personal protective equipment.
Requirements
- 2â€"3 years of experience in a GMP-regulated QA role (pharma or chemical industry).
- Strong understanding of GMP principles and documentation practices.
- Comfortable working in cleanroom conditions and wearing PPE.
- Proficient in Dutch (mandatory) and English.
- Education level to be confirmed (background in pharma or chemical industry preferred).
- Experience with ISO 9001, ISO 22000, ISO 13485 is a plus.
Other Information
Role expansion due to GMP department growth
Increasing automation in filling processes (transition from manual to robotic systems)
No shift work, standard 40-hour work week.
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