Quality Assurance Specialist
Tataa Biocenter AB / Kemistjobb / Göteborg
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hela Sverige Who Are We?
TATAA Biocenter is a rapidly growing specialized CRO offering services to pharma and biotech customers and is considered a leader in the field. With a team of scientists providing laboratory services in genomics, transcriptomics, and proteomics across a broad range of molecular analysis technologies including qPCR, digital PCR, NGS and, Olink, TATAA offers method development, assay validation and sample analysis services. Our laboratory is GLP- ready and ISO 17025 accredited, and also performs research-grade assays. Join us and become an integral part of our dynamic team, contributing to advancements in molecular analysis.
Publiceringsdatum2024-01-23ArbetsuppgifterAbout The Role
As a QA Specialist at TATAA, you will be at the heart of our commitment to maintaining the highest standards of quality in our operations. We are seeking a committed and detail-oriented individual to ensure that our processes and outputs meet our customers demands, regulatory requirements and industry best practices. This is an exciting opportunity to be part of a team dedicated to advancing groundbreaking solutions in molecular analysis.
Your Essential Responsibilities as a QA Specialist at TATAA will Include:
• Collaborate in implementing and maintaining a cutting-edge Quality Management System (QMS) aligned with GLP guidelines and ISO 17025 standards.
• Actively engage in internal audits and inspections to ensure strict adherence to GLP, ISO 17025, and other regulatory requirements.
• Assist in the preparation for external audits and inspections and help address any identified non-conformities.
• Review and approve laboratory documentation, including SOPs, validation protocols, and test reports, ensuring they meet and exceed our meticulous quality standards.
• Monitor and record quality-related data, actively contributing to the analysis to identify trends and areas for continuous improvement.
• Support the Head of QA and the QA team in managing and resolving quality-related issues, playing a key role in the implementation of corrective and preventive actions.
• Contribute significantly to the training and development of staff on quality-related matters, including GLP and ISO 17025 requirements.
• Stay updated on GLP regulations, ISO 17025 standards, and other relevant quality benchmarks, ensuring our practices remain at the forefront.
• Actively participate in risk management activities, offering insights for continuous improvement and contributing to the implementation of changes aimed at enhancing quality and efficiency.
• Demonstrate attention to detail by preparing and submitting regular quality reports, providing key insights into our performance and adherence to the highest standards.
• Review and approve study protocols and reports, ensuring accuracy and excellence.
KvalifikationerQualifications and Attributes Who Are You?
Are you someone who:
• Hold a bachelors degree in a relevant scientific field with 3 years of experience.
• Possess a knowledge of GLP regulations, ISO 17025 standards, and other relevant quality standards.
• Demonstrates experience in conducting internal audits.
• Exhibit strong commitment to maintaining high standards of quality and dedication to continuous improvement.
• Showcase exceptional attention to detail in all aspects of work.
• Hold good communications skills, enabling effective collaboration and coordination with cross-functional teams.
• Ability to work effectively under pressure and adapt to changing priorities.
• Strong self-motivational drive for shared success of the team and company.
ÖVRIGT
Joining our team at TATAA means being part of a dynamic and collaborative environment committed to accelerating innovations in precision medicine to improve lives. If you are a dedicated professional with a passion for quality assurance, we invite you to apply for this exciting opportunity.
Position: Fulltime
Placement: Gothenburg, Sweden
Start date: Upon agreement
Please note that submission of both CV and cover letter is required.
We will screen the applications continuously and close the process when we have found the right candidate.
We respectfully decline offers from recruitment or staffing agencies for this recruitment process. Thank you for your understanding.
Visit us on
https://tataa.com/If you have any questions, you are most welcome to contact our Head of QA, Per Wormbs, +46 72 16 34 230.
Ersättning Enligt avtal.
Så ansöker du Sista dag att ansöka är 2024-02-23
Klicka på denna länk för att göra din ansökan Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "C174183".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Tataa Biocenter AB (org.nr 556640-7143)
Arbetsplats Tataa Biocenter AB
Kontakt TATAA Biocenter AB
jobs@tataa.com Jobbnummer 8412306
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