Cơ bản

QC Analyst – Cleaning Verification & Validation (Helsingborg)

Helsingborg, Skåne County, Sweden Công ty: TN Sweden Khách hàng / Nhà tuyển dụng: WeQuel
Đã đăng: 22.05.2026
Ngày kết thúc: 06.07.2026
Giới thiệu công việc: aeff5902c28a898f2e13223f08849726

Thông tin việc làm

Địa điểm
Helsingborg, Skåne County, Sweden
Công ty
TN Sweden
Khách hàng / Nhà tuyển dụng
WeQuel
Giới thiệu công việc
aeff5902c28a898f2e13223f08849726
Loại thông tin đăng tải
Cơ bản
Yêu cầu giấy phép lao động EU
Không
Đã đăng
22.05.2026
Ngày kết thúc
06.07.2026

Mô tả công việc

WeQuel sammanför ambitiösa företag med exceptionella människor inom Life Science, Engineering och IT.Genom specialistkompetens, starka relationer och ett långsiktigt perspektiv hjälper vi organisationer att bygga högpresterande team som driver innovation, affärsutveckling och operationell excellens.Vi tror att framgångsrika företag byggs av rätt människor och att starka samarbeten skapar långsiktig påverkan.About the RoleAs a QC Analyst, you will be responsible for both routine and project-based analytical activities related to cleaning verification and validation. You will play a key role in ensuring product quality and compliance, working closely with cross-functional teams within Quality, Manufacturing, and Validation.Key ResponsibilitiesPerform cleaning verification and cleaning validation in accordance with approved methods and protocolsExecute analytical testing using HPLC and GC techniquesDocument and review results in compliance with GMP standards and data integrity requirementsInvestigate and troubleshoot analytical results and laboratory methods when necessaryEnsure adherence to internal SOPs and regulatory requirementsContribute to continuous improvement of laboratory processes and documentation practicesCollaborate cross-functionally with relevant stakeholdersRequirements (Must Have)Proven experience working as a QC Analyst in a GMP-regulated environmentHands-on experience with cleaning verification and/or cleaning validationStrong practical experience with HPLC and GCSolid understanding of GMP, documentation practices, and data integrity principlesAbility to work independently, in a structured and detail-oriented mannerFluent in English, both written and spokenPreferred QualificationsExperience within pharmaceuticals, consumer health, or life sciencesPrevious experience working as a consultantExperience with method validation, method transfer, or troubleshootingExperience collaborating closely with Validation or Manufacturing teamsFamiliarity with LIMS or similar laboratory systems

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