OverviewBioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.About Technical OperationsBioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.RoleQC Analyst – In‑Process Control (Shift Role)Location: BioMarin – QC In‑Process | 4‑Cycle Shift PatternAn exciting opportunity has arisen for a QC Analyst to join BioMarin’s QC In‑Process Control team, based in a newly 5S‑certified analytical laboratory. This role offers excellent exposure across both Drug Substance and Drug Product manufacturing, in a fast‑paced, highly compliant GMP environment.The QC In‑Process team delivers comprehensive in‑process analytical and microbiological testing, supporting manufacturing operations across the site. In addition, the team performs testing of incoming raw materials and packaging materials to support downstream pack line activities.Due to the critical, around‑the‑clock nature of in‑process testing, this role is part of a 4‑cycle shift team, supporting continuous manufacturing operations.QC In‑Process is a high‑performing, team‑based group, where colleagues are flexible, multi‑skilled, and empowered to make decisions. The team operates to an exceptionally high standard of quality, compliance, and safety, with a strong focus on continuous improvement, standard work, and 5S.This role requires a high level of initiative, energy, and motivation, together with strong organisational skills and the ability to thrive in a dynamic manufacturing environment.ResponsibilitiesPerform primary review of QC raw data and trend resultsPrepare protocols, summaries, and reports, including documents submitted directly to pharmaceutical regulatory agenciesDraft and update QC Standard Operating Procedures (SOPs)Act as a technical subject matter expert (SME) and provide training and support to other analysts in areas of expertiseEvaluate analytical and microbiological results against defined acceptance criteriaConduct and document laboratory investigations through to completionMaintain the laboratory in a constant state of audit and inspection readinessInteract directly with regulatory agency inspectors during audits and inspectionsInterface with other BioMarin functions including Manufacturing, Quality Assurance, Facilities, and external contractors as requiredOther duties as assignedDesirable Skills and AttributesExcellent written and verbal communication skillsStrong customer focus, with personal accountability for speed, quality, and accuracy of deliverySelf‑motivated, with the ability to work under pressure in a fast‑paced environmentTeam‑oriented, with active participation in team development and continuous improvement, including standard work and 5SDemonstrated success in achieving goals as part of a high‑performing team in a growing organisationProven adaptability and flexibility to support an evolving operational environmentEducation and ExperienceBSc in a scientific or engineering discipline with 5+ years of relevant cGMP laboratory experience orMSc with 3+ years of relevant cGMP laboratory experienceNote: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.Equal Opportunity Employer/Veterans/DisabledAn Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
#J-18808-Ljbffr