NL Specialist Quality Assurance
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Equipment Validation Specialist voor farmaceutische productie in Breda, 12 maanden, start december.
- Locatie
- Breda
- Werkvorm
- op locatie
- Uren
- 40 uur per week
- Contractvorm
- detachering
- Startdatum
- Eerste waarneming
- Opdrachtgever
- A dynamic organization operating in the pharmaceutical or biotech manufacturing sector
Eisen
- Comfortable working within a team of junior professionals, providing guidance as needed
- Strong expertise in equipment validation and documentation review
- Minimum of 5 years of professional experience in GMP environments, specifically in equipment validation
- Strong communication skills and a structured, organized approach to work
- Proven ability to work independently and deliver high-quality results
- Excellent attention to detail and ability to handle large amounts of technical documentation
- Experience with quality review of validation packages and risk management tools
Omschrijving
We are seeking an experienced Equipment Validation Specialist to join a technical support team responsible for ensuring the integrity and compliance of manufacturing equipment and systems. This role involves managing validation activities for existing production equipment, providing expert review, and supporting quality and regulatory standards. Responsibilities: Lead and support equipment validation activities independently across existing production lines. Review and approve validation documentation, ensuring compliance with internal standards, GMP, and regulatory requirements. Support technical documentation and validation deliverables, maintaining accuracy and completeness. Assist in risk assessments related to equipment and validation processes, identifying potential issues and mitigation strategies. Review validation data, change requests, and validation investigations, ensuring high-quality documentation. Collaborate with cross-functional teams, providing technical guidance and ensuring validation processes align with quality policies. Support deviation investigations, CAPAs, and continuous improvement activities related to validation. Requirements: Minimum of 5 years of professional experience in GMP environments, specifically in equipment validation. Strong expertise in equipment validation and documentation review. Proven ability to work independently and deliver high-quality results. Experience with quality review of validation packages and risk management tools. Excellent attention to detail and ability to handle large amounts of technical documentation. Strong communication skills and a structured, organized approach to work. Comfortable working within a team of junior professionals, providing guidance as needed. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me. Candidates who are motivated by long-term roles, have a flexible approach to relocating or commuting within approximately one hour, and are available for a December start are encouraged to apply. The initial contract is for 12 months with a strong possibility of extension, supporting a collaborative and innovative work environment.
Alle opdrachtenBekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Gegevens automatisch overgenomen uit de oorspronkelijke publicatie; controleer de details bij de bron. Wij zijn geen partij bij de aanvraag. Hoe wij werken.