Asaja Empleo. Ofertas de trabajo

We are looking for a Protein Mass Spectrometry Scientist to be incorporated in our department of Innovation.

She/he will participate in the development and validation of assays and sample analysis for qualitative and quantitative analysis of the proteins using liquid chromatography coupled to mass spectrometry techniques using QTOF and triple quadrupole systems.

Examples of the assays to be performed are:

• Entire mass of determination proteins and peptides
• Peptide mapping and amino acid sequencing of protein and peptides
• Identification and quantitation of peptide and protein impurities
• Some specific mass spectrometry studies of other kink of molecules (small molecules, glycosaminoglycans, etc.)

Buscamos a analistas para nuestro departamento de Control de Calidad, donde se analizan principalmente materias primas, producto acabado y especialidades farmacéuticas.

Las responsabilidades son:

• Dar soporte a los químicos analíticos en la preparación de muestras y en el uso de diversas técnicas analíticas (potenciometrías, Karl Fisher, Cromatografia Líquida de Alta Resolución (HPLC), cromatografía de gases, UV, Test de disolución, etc)
• Realizar el trabajo en un entorno de cumplimiento de Buenas Prácticas de Laboratorio y GMP.

We are looking for analysts for our Quality Control Department, where we analyze mainly raw materials, finished products and pharmaceutical specialties.

The responsibilities of the position are:

• Support analytical chemists in the preparation of samples and the use of various analytical techniques (potentiometries, Karl Fisher, high performance liquid chromatography (HPLC), gas chromatography, UV, dissolution test, etc)
• Perform the work in an environment of compliance with Good Laboratory Practices and GMP.

We are looking for a Scientist for our Biologics Quality Control Department.

Under the supervision of the Department Manager, the Scientist will be responsible for the following duties:

• The design, supervision and execution of quality control studies of Biological Products including chromatography and HPLC. At least 3 years of experience with these techniques is required.
• The management of the assigned projects keeping the deadlines and establishing a direct communication with the client
• Technical document management associated with the studies ( standard procedures, certificates of analysis, deviations, OOS’s, CAPA’s, etc.)
• The direction and supervision of the experimental work of the technical staff in charge.

At Kymos, we want to ensure that we attract the best professionals in the industry. That's why we have opened a job posting that is open to all types of scientific profiles.

We are seeking talented and passionate professionals in the fields of chemistry, biotechnology, biochemistry, and analysis, including recent graduates and experienced individuals. We are also looking for analysts from various backgrounds who are committed and focused on providing support.

If you are an expert in your field or a PhD with specialized knowledge, we would love to get to know you!

As a member of our team, you will have the opportunity to work on challenging and diverse projects for clients worldwide. You will be part of a dynamic and collaborative environment where you can develop your skills and grow professionally.

Responsibilities:

• Conduct high-quality scientific research and analysis.
• Collaborate with the team in project planning and execution.
• Maintain accurate records and scientific documentation.
• Interpret and effectively communicate the results of analyses.

We are hiring a Qualified Person (QP) for our Quality Assurance Department

The Qualified Person (QP) will be assigned the following responsibilities:

• Review and approve the documentation involved in the analytical activity of the company: CoA, Site Master File, SOPs, product specifications.
• Participate and be involved in the revision of manufacturing batch records and packaging batch records and other batch review documents of products to be released.
• Participate in the certification of batches susceptible to be released to the market (QP release) and ensuring the application of the GMP according to the marketing authorization of the finished drug product-
• Participate in the certification of investigational medicinal product batches susceptible to be released for a clinical trial and ensuring the application of the GMP according to the investigational medicinal product Dossier.
• Participate in the evaluation of deviations, OOS/OOT, complaints, CAPA and Change Controls.
• Review of the review of Quality/Technical Agreements between the company and subcontractors, especially with regard to batch certification activities.
• Collaborate in audits carried out by our clients or subcontracted manufacturers and give support in the Inspections of regulatory authorities.
• Participate in the implementation and improvement of the quality of the company and subcontractors.

We are looking for a CFO Assistant to join Kymos Group.

You will be a key member of our Finance and Administration team and be supporting our 3 sites in Spain, Germany, and Italy. You will be in charge the day-to-day supervision of each area of department ensuring the compliance of with policies and procedures, as well to implementation of new policies or procedures.

Your role will be to support the CFO of the company in all tasks related to the management of the areas related to the department, you will report to our financial director and have the following responsibilities of Group:

• Review, supervision and negotiation about all direct and indirect expenses, outsourcing services, and Group contracts.
• Participate in the preparation and consolidation of the annual budget and its forecasts or periodic reviews.
• Participate in the monitoring indicators of the expenses of activity and control of its application.
• Carry out the reporting (monthly, quarterly, annual), seeing its consistency with the accounting and management reports and the possible deviations and risks.
• Make and apply plans or recommendations to reduce costs.
• Optimize management information systems.
• Responsible of develop and implement the system of flows, SOP’s, procedures, good practices of the department.
• Recommend and implement process improvements to achieve better results.
• Support to different department areas.
• Control accruals and deferrals.
• Intercompany management services, and coordination all the information of different companies.
• Capex evolution, following, reporting.

The QA Scientist will be assigned the following responsibilities:

• Be involved in the revision of manufacturing batch records and packaging batch records and other batch review documents of pharmaceutical products to be released.
• Participate in the evaluation of deviations, OOS/OOT, complaints, CAPA and Change Controls of pharmaceutical products to be released ensuring the application of GMPs and according to the marketing authorisation or clinical trail authorisation.
• Participate in the certification process of batches susceptible to be released to the market or for clinical trials.
• Review of Quality/Technical Agreements between the company and manufacturers and marketing authorisatio holders, especially with regard to batch certification activities.
• Review and approve the documentation involved in the activity of the company: CoA, Site Master File, SOPs, product specifications.
• Collaborate and participate in the revision of audit reports carried out by third-parties to the manufacturers of pharmaceutical products to be released.
• Collaborate in audits carried out by our clients and give support in the Inspections of regulatory authorities.
• Participate in the implementation and improvement of the quality system of the company.