Jobid=2e20d1e83a3c (0.0376)
Job Summary
The role focuses on managing the lifecycle of laboratory equipment and systems within a regulated GMP environment. The position involves leading equipment introduction and implementation projects, ensuring systems are properly installed, validated, maintained, and decommissioned where required. The specialist works across multidisciplinary teams to manage project timelines, maintain data integrity, support laboratory operations, and ensure compliance with relevant regulatory standards such as GMP, GAMP, and USP. The role also involves maintaining validation documentation, coordinating with vendors on new technologies, and contributing to continuous improvement initiatives within laboratory services.
Essential Requirements
- Proven experience working in the pharmaceutical industry within a GMP environment.
- Experience managing projects, including budgeting, planning, resourcing, and stakeholder coordination.
- Ability to lead multiple projects simultaneously from initiation through to completion.
- Strong organisational skills with the ability to prioritise tasks and manage competing deadlines.
- Ability to work proactively and independently, including writing protocols, reports, procedures, and business correspondence.
- Strong analytical and technical problem-solving skills.
- Effective communication skills with the ability to engage with stakeholders at different organisational levels.
- Fluency in written and spoken English.
Preferred Requirements
- Laboratory experience.
- Experience with Computer System Validation in a GxP environment.
- Familiarity with laboratory software systems such as Empower, Softmax Pro, SDMS, Deskman, LIMS, 32Karat, Trackwise, Comet, or KNEAT.
- Knowledge or experience with Lean or Six Sigma methodologies.
- Dutch language skills.
Practicalities
- Location: Leiden, Netherlands
- Contract duration: 12 months
- Working hours: 40 hours per week
Interested? Apply now or send your CV to l.ormrod@panda-int.com
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