Senior Quality Control Analyst

Are you an experienced QC professional looking to step into a senior role within a GMP-regulated environment?Smart4 Sciences are partnering with a leading global organisation specialising in pharmaceutical excipients and film coating systems to recruit a Senior QC Analyst for a permanent position based in Almere, Netherlands.This is an excellent opportunity for a QC professional with strong analytical experience and leadership exposure who enjoys working in a fast-paced, quality-driven environment while contributing to the release of high-quality materials used across the pharmaceutical supply chain.Key Responsibilities:Lead and perform sampling, testing, and reporting activities for raw materials, intermediates, and finished products in line with GMP and ALCOA+ principlesConduct chemical, physical, and instrumental analysis using approved analytical techniques (e.g. particle analysis, viscosity, moisture testing)Review analytical data for accuracy, completeness, and compliance with regulatory and internal standardsSupport and oversee environmental monitoring activitiesInvestigate and document deviations, OOS/OOT results, and non-conformances, supporting root cause analysis and CAPA activitiesMaintain laboratory operations including calibration, equipment troubleshooting, and inventory managementEnsure all documentation complies with GDocP and data integrity requirementsSupport audits and inspections, maintaining a constant state of inspection readinessMentor junior team members, support onboarding of new starters, and provide technical guidanceCollaborate with internal teams and external laboratories to ensure timely and accurate reportingIdeal Candidate:Degree (MBO+ or equivalent) in Chemistry, Laboratory Sciences, or a related disciplineProven experience within a GMP-regulated environment (pharmaceutical, excipients, medical devices, or food manufacturing)Strong hands-on experience with analytical testing and data interpretationPrevious experience mentoring, supervising, or supporting junior team membersSolid understanding of GMP, GLP, GDocP, and data integrity (ALCOA+) principlesStrong attention to detail, problem-solving skills, and ability to manage deviations effectivelyConfident communicator with the ability to work both independently and collaborativelyWhy Apply?Join a globally recognised organisation with a strong reputation in the pharmaceutical industryOpportunity to step into a senior, influential QC role with leadership responsibilitiesWork in a highly collaborative, quality-focused environmentBe part of a company committed to continuous improvement and innovation