ofertas en life sciences en barcelona.

Sales Team Leader ( Spain )

25 febrero 2021

Randstad Professionals , Barcelona (Barcelona)

Indefinido

The company specialized in the development, production and distribution of automated workflow solutions for laboratories in the life sciences sector. Objectives: Supports the company mission and goals by directing all sales operations in the Spain.  Managing the Salesteam, Distributors and Key Accounts.- Builds strategies and formulates sales plans to achieve regional business and financial growth objectives.- Actively lead, manage, support and develop assigned sales team to achieve defined goals and objectives.- Active management of Partners and Distributors.- Develop and implement KAM plans for selected Key Accounts, ensuring agreed goals are exceeded. Tasks: Devises and formulates regional (Country) growth plan in line with the overall company objectives.- Ensures regional sales growth and profitability targets are exceeded.- Manage, appoint, and release Distributors based on performance, ensuring targets are exceeded.-  Ensure Key account sales growth and profitability targets are exceeded.-  Actively Forecasts Order Entry and Sales and present to Management in a timely fashion.- Monitors commercial performance through regional KPI.- Implements action plans to ensure meeting commercial objectives.- Networks with key opinion leaders and partners to drive the business. Actively work with local authorities.- Actively participates in Sales meetings and conferences to give direction and feedback to the team onperformance and expectations.- Lead sales team providing guidance and tools to allow the team to operate successfully and effectively. Inparticular the use of the company¿s CRM system.- Take responsibility for regional leadership and sales team development.- Attract, retains and develop talent.- Ensure the company¿s code of conduct, compliance to company¿s values and business processes areadhered to.- Provides regional market intelligence into strategy. Responsabilities: Accountable for overall business performance in the region/country.  Accountable for all direct sales, distributor and KAM operations of the regions.  Responsible for Sales Team, KAM Business and Distributors within the Region/Country.

Delegado Visita Farmacia

24 febrero 2021

Randstad Professionals , Barcelona (Barcelona)

Indefinido

Reportando a director comercial, el/la candidato/a seleccionado/a será el encargado de gestionar las farmacias de la zona asignada (Provincia de Barcelona). Entre sus funciones destacan:-Planning y organización de visitas a farmacias de la zona.-Análisis y segmentación de clientes.-Soporte a farmacia con información técnica y científica.-Control de stock en farmacias.-Participación en eventos-Soporte a formadores en farmacias y parafarmacias.-Reporting actividad diaria.

Mantenimiento

23 febrero 2021

Randstad , Sant Vicenç dels Horts (Barcelona)

Indefinido, 20.000-21.000€ al Año

¿Tienes experiencia en mantenimiento? En Randstad buscamos gente como tú! Reconocida empresa en plena expansión internacional. Desarrollo y ejecución de trabajos de mantenimiento y reparaciones Resolución de incidencias y averías Instalación de nuevos equipos Acciones correctivas Construcción de pequeños utillajes 

Product Transfer Specialist

18 febrero 2021

Randstad Professionals , Barcelona (Barcelona)

Indefinido, 35.000-40.000€ al Año

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.

Manipulador turno noche

18 febrero 2021

Randstad , Sant Vicenç dels Horts (Barcelona)

Con posible incorporación a plantilla, 9-10€ la Hora

¿Tienes experiencia en manipulación y control de calidad en sector cosmético, farmacia o química? Buscamos gente como tú! Reconocida empresa en constante crecimiento. Control calidad producto Envase de producto Manipulación de producto

Operario farmacéutico

16 febrero 2021

Randstad , Sant Boi de Llobregat (Barcelona)

Temporal, 18.600-18.700€ al Año

¿tienes experiencia en departamento de envasado/acondicionado en empresas del sector Pharma/Química/Cosmética? Buscamos personas como tú! Empresa farmacéutica internacional, centrada en la investigación científica, especializada en desarrollar y producir medicamentos genéricos. - Cumplir las instrucciones de trabajo.- Abastecer las líneas de envasado (emblistadoras, botes o sobres).- Cumplimentar la documentación requerida.- Realizar el cambio de formato de la línea a su cargo, así como de los ajustes básicos, la preparación y finalización de órdenes de trabajo.

Técnico/a de Procesos de Síntesis (Química Orgánica)

07 enero 2021

Randstad Professionals , Mataró (Barcelona)

Indefinido

Importante compañía ubicada en el Alt Maresme (Barcelona) desea incorporar un/a Técnico/a de Desarrollo (especialidad en química orgánica). La persona seleccionada se integrará en el equipo de Desarrollo para participar en proyectos de desarrollo de producción química a gran escala.Principales responsabilidades: Diseñar, adaptar y ejecutar procesos de síntesis química y métodos de purificación a escala de laboratorio para cubrir con los requerimientos de producción en la planta química.

Regulatory Affairs Specialist

16 diciembre 2020

Randstad Professionals , Barcelona (Barcelona)

Indefinido

Be part of a constanly growing biological multionational. We offer attractive conditions and the opportunity to build a professional career. Our client, an international biotechnology company, is looking for a REGULATORY AFFAIRS SPECIALIST for a permantent project in the outskirts of Barcelona, Spain. This position provides effective regulatory support for company¿s manufactured products and customer¿s products. Prepare and submit the documentation according to the corresponding legislation for the different countries. Be responsible for the implementation of new regulatory requirements. Key Accountabilities - Prepare the required documentation to obtain the CE mark, FDA or other country registrations for the company¿s manufactured products or customer¿s products in accordance to the current legislations. Communication and maintenance of products with Spanish authorities. - Support customers with any regulatory aspect. - Follow-up and resolve the requirements emerged in the registration procedures. - Maintain technical files as necessary to sustain product approval. - Review product materials, labeling and/or specification sheets for compliance with applicable regulations and customer¿s policies. - Be part of the CFT projects as the RA representative. - Support internal and external audits, validations and product¿s risk analysis. - Follow management indicators/metrics for the proper performance of the department and apply, if necessary, the appropriate corrective actions. - Support the Market Surveillance Department in the compilation of information for the Post Market Surveillance. - Recommend and manage, if applicable, changes to company procedures/documents (quality system and compliance) to comply with current regulations, guidelines and/or standards. - Provide support to Customer Service regarding import/export of the products. - Ensure effective partnering and collaboration with R&D, Quality Operations, Design Quality and Operations to meet project goals, maintain compliance, and complete defined regulatory submissions. - Ensure that all documentation is RA reviewed before it is shared externally with regulators and/or customers. - Collaborate with other QRA groups, R&D, and Operations to ensure successful Regulatory Inspections

Biotechnology Manufacturing Aos Group Coordinator

30 noviembre 2020

Randstad Professionals , Lliçà d'Amunt (Barcelona)

Indefinido, 35.000-40.000€ al Año

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.

Product Release Manager

26 noviembre 2020

Randstad Professionals , Barcelona (Barcelona)

Indefinido

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.