ofertas de técnico calidad en life sciences.

3 trabajos

ofertas de empleo de Técnico calidad en Life sciences

¿Buscas trabajo de Técnico calidad en Life sciences? Contamos con miles de ofertas de empleo cada día: en alta dirección, mandos intermedios, puestos técnicos, posiciones temporales; en diferentes jornadas y horarios; que requieren o no experiencia, para que puedas apuntarte a la que mejor se adapte a tu perfil ¡Inscríbete!

3 trabajos encontrados de Técnico calidad en Life sciences

  • Product Transfer Specialist

    18 febrero 2021

    Randstad Professionals , Barcelona (Barcelona)

    Indefinido, 35.000-40.000€ al Año

    company

    Our client, an international biotechnology company, is looking for a PRODUCT TRANSFER SPECIALIST for a permantent project in the outskirts of Barcelona, Spain. As Product Transfer Specialist will be responsible for transfer and process validation of new products including manufacturing records, validation protocols & reports and other current Good Manufacturing Practice (cGMP) documents, e.g., Standard Operating Procedures (SOPs), Work Instructions (WIs) used in the execution of manufacturing processes and/or other operations areas. The selected candidate will work very closely with different departments (R&D, Manufacturing, Engineering, Supply Chain, Technical Support, Quality Operations, Quality Control, Regulatory Affairs and Sales and Marketing). The position requires good understanding of process validation under cGMP regulated environment. Key Responsibilities ¿ Responsible for transfer and process validation activities starting at Feasibility phase and ending at Launch Phase (including manufacturing documentation and validation protocols and reports). ¿ Participate actively in NPD, enabling to identify scale-up challenges early on during feasibility. Primary aims are to make the process safe, scalable, robust and reproducible while targeting at increasing yields and throughput. ¿ Assess the production equipment required for the manufacturing of new products. ¿ Ensure best practices are implemented in the new product development. ¿ Review feasibility deliverables and perform assessments to evaluate transfer readiness. ¿ Develop new Manufacturing Procedures and other high-quality documentation that meets applicable standards/ requirements of the users. Write and edit technical information/ instructions in a manner to ensure content is factual and accurate. ¿ Manage the lifecycle of Manufacturing Records including, but not limited to creation, review, revision and approval until the product launch. ¿ Communicate actively to address user comments and to clarify users questions with respect to technical documents. ¿ Ensure manufacturing documentation follows the section template/ structure. ¿ Maintain a system for tracking changes to be implemented in all upcoming products. ¿ Deliver documents with strict adherence to the production schedule . ¿ Provide assessments and insights to Change Requests from the manufacturing section and/or R&D perspective. ¿ Ensure assigned CAPAs, deviations, non-conformities and Change Controls related to validation lots and FLTS are closed in a timely manner. ¿ Attend planning and cross functional team (CFT) meetings. ¿ Perform any other duties as assigned by the Lead / Manager.

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  • Biotechnology Manufacturing Aos Group Coordinator

    30 noviembre 2020

    Randstad Professionals , Lliçà d'Amunt (Barcelona)

    Indefinido, 35.000-40.000€ al Año

    company

    Our client, is a recognized and renowned company with consolidated experience worldwide in research, development and manufacturing of Assay and Biomaterilal solutions for IVD use. The Biotechnology Manufacturing AOS Coordinator is responsible for coordinating all activities related to biotechnology manufacturing processes adaptations, optimizations, scale up and trouble shooting. Those activities include, among others, coordination of experimental phase, AOS team management and perform the corresponding documental tasks. The Biotechnology Manufacturing Section embraces different technologies such as, among others, cell culture, virology, recombinant proteins (eukaryotic and prokaryotic systems) and protein (antigens and antibodies) chromatographic purification. Key Accountabilities: - Coordinate AOS technical related activities: experimental design, scheduling, execution, data and project analysis, report writing.o A: Adaptation. Related to process transfer from third parties. Leading any adaptation required in the project to fit to Biokit MFG characteristics.o O: Optimization. Current manufacturing processes improvement when needed. Trouble Shooting.o S: Scale up: Current manufacturing processes scale up, when needed.- Supervise AOS team technicians.- Manage interactions with Departments related to AOS projects.- Manage and follow up, in coordination with Quality Assurance, of Non Conformities that give rise to AOS activities. To Update Manufacturing SOP¿s when needed because of AOS activities.- Achieve performance goals agreed with Section Management.- Innovation. Stay updated on the latest technologies related to biotechnology manufacturing.

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  • Product Release Manager

    26 noviembre 2020

    Randstad Professionals , Barcelona (Barcelona)

    Indefinido

    company

    We are looking for a Product Release Manager for an important Biotech Company. The position is responsible for performing Quality Operations oversight of GMP compounding activities at the company. The position performs the quality review of batch records for final products, reviews and evaluates QC data, and evaluates process validations to ensure that lots meet applicable GMP requirements prior to release.Key accountabilities:- Review executed batch records, and associate documentation for compliance with GMP ans consistency with policies and procedures.- Coordinate lot release with Operations and Warehouse management to ensure efficient and on time release od products batches.- Review and evaluate QC data for release and approval of batch records.- Record and trend Quality data related to final release of product.- Assisting in the development of SOPS, Batch Records and review checklist for compliance with GMPS.- Evaluate team priorities and recommends improvements.- Participate in audits, investigations, SOP preparation, CAPA´s and other projects as appropiate.

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