Continuous Improvement Specialist
Key Skills
Job Description
The Company Our client is a leading pharmaceutical company committed to delivering high-quality products through innovative processes and rigorous standards. They focus on continuous improvement and patient safety, maintaining excellence across all facets of their operations. Job Description As a Continuous Improvement Specialist, you will drive Lean and continuous improvement initiatives within a manufacturing environment, focusing on process optimization, efficiency, and performance improvement. You will implement Lean tools, analyze KPIs, standardize processes, and collaborate with cross-functional teams to deliver measurable improvements while maintaining daily production targets. Responsibilities Implement Lean and Continuous Improvement initiatives to improve manufacturing efficiency, productivity, and process performance. Analyze manufacturing processes and KPIs to identify inefficiencies, root causes, and opportunities for improvement. Develop and implement Lean tools, including standard work, work combination charts, and training matrices. Establish performance tracking and governance to monitor improvement results and support data-driven decisions. Collaborate with cross-functional stakeholders to standardize processes, share best practices, and support continuous improvement projects. Support change controls, quality investigations, and process documentation while maintaining daily production and shipment targets. Requirements Relevant HBO degree with approximately 3 years of experience in Continuous Improvement, Operational Excellence, or Manufacturing Process Improvement. Hands-on experience implementing Lean methodologies and delivering measurable improvements in a manufacturing environment. Lean Six Sigma Black Belt certification or equivalent practical experience leading improvement initiatives. Experience with KPI tracking, process analysis, standard work, root-cause analysis, and process standardization. Experience with change controls, CAPA, deviations, or quality investigations; pharmaceutical or other regulated manufacturing experience is an advantage. Other Information Apply to our vacancy for more information. We look forward to hearing from you!
Core Responsibilities
Lead Lean and continuous improvement initiatives to improve manufacturing efficiency, productivity, and process performance while meeting daily production and shipment targets. Analyze KPIs and processes, implement standardization and performance tracking, and collaborate across teams on improvement projects, change controls, and quality investigations.
Requirements
Requires a relevant higher professional education degree and approximately three years of experience in continuous improvement, operational excellence, or manufacturing process improvement. Candidates should have hands-on Lean experience, Lean Six Sigma Black Belt certification or equivalent practical experience, and familiarity with KPI tracking, root-cause analysis, process standardization, and quality processes such as CAPA or deviations.
About SIRE® Life Sciences 🧬
Industry: Biotechnology Research
Company size: 201-500 employees
SIRE® Life Sciences is the market-leading partner for Life Sciences consultancy, project management, and secondment services in the Netherlands. We specialize in connecting expert consultants and project managers with leading biotech, pharmaceutical, medical device, clinical research, and food technology organizations. Our services include: - Life Sciences recruitment & executive search - Interim management & secondment - SOW-based project outsourcing & delivery - RPO (Recruitment Process Outsourcing) - MSP workforce management & vendor-neutral solutions - GMP, GCP, GLP compliance staffing - Clinical research & regulatory affairs resourcing With 100,000+ professionals in our network and 25+ years of experience, SIRE® Life Sciences delivers measurable results for regulated organizations across the Netherlands and Europe. We work with pharma, biotech, medical device, CDMO, CRO, and food technology companies at every stage of the product lifecycle. What sets us apart: - Deep domain expertise in Life Sciences & regulated industries - Full compliance with GxP, ISO, WAADI, and Dutch labour law - Flexible engagement models: permanent, interim, project (SOW), and managed services - Proven delivery track record across Pharma, Biotech, MedTech & Food Science Based in Leiden Bio Science Park, Netherlands. www.sire-search.com