Empleos de Veg Group en España

Job Description: · Evaluate compendial changes from different pharmacopeias. · Generate trend reports of investigations based on company procedures. · Evaluate global documents against site-specific procedures and update them accordingly. · Draft technical documents such as metho ...

The Validation Specialist will be responsible for ensuring that all manufacturing equipment is qualified and validated to meet regulatory requirements. · Key responsibilities include: · Developing and executing IQ/OQ/PQ protocols · Performing Factory Acceptance Testing (FAT) and ...

MF CQV Scientist for Biotech Manufacturing Equipment · La experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación. · Validation & Engineering Group, Inc. · (V&EG) is a leading s ...

A key role for a Quality Control Scientist III is available with our client company providing pharmaceutical services. Ideal candidates will have at least 8 years of experience in quality control of medicines. · About the Role: · Evaluate compendial changes and generate reports; ...

Project Manager Job Description · A leading services supplier in Barcelona seeks a skilled Project Manager with over 5 years of experience and GMP knowledge. · Manage projects concerning Process Equipment and Clean Utilities. · Collaborate with teams, develop plans, monitor progr ...

Job Description · The Validation & Engineering Group, Inc. (V&EG) is seeking a Quality Control Scientist III. · Evaluate compendial changes from different pharmacopeias, · Generate trend reports of investigations based on company procedures, · Draft technical documents such as me ...

Career Opportunities with Validation & Engineering Group · Si sus habilidades, experiencia y cualificaciones coinciden con las de esta descripción del puesto, no demore su solicitud. · A great place to work. · Current job opportunities are posted here as they become available. · ...

We are seeking an experienced Commissioning, Qualification and Validation (CQV) Scientist to qualify equipment within a Quality Assurance (QA) Laboratory. · Key Responsibilities: · Ensure compliance with Good Manufacturing Practices (GMP) · Deliver projects on time and within bud ...

A leading services supplier in the pharmaceutical sector is seeking a Quality Control Scientist III in Barcelona. · Presente su candidatura después de leer los siguientes requisitos de habilidades y cualificaciones para este puesto. · This role requires a Bachelor's Degree in Sci ...

Job Description · We are seeking a self-sufficient Validation Engineer to support a downstream biologics validation project at a cGMP manufacturing site in Puerto Rico. · ...

Project Manager · We seek a skilled Project Manager with GMP experience preferably in OSD, over 5 years of project management experience. · Bachelor's degree in Engineering or related field. · PMP certification preferred. · ...

Validation & Engineering Group, Inc. · Es esencial asegurarse de que cumple con los requisitos como solicitante para este puesto; por favor, lea atentamente la información a continuación. · (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biote ...

CQV Scientist for Biotech Manufacturing Equipment · This role is responsible for ensuring compliance with regulatory requirements in biotech manufacturing facilities. · Develop Systems Development Life Cycle (SDLC) documents such as VP, URS, DS, RA, IQ, OQ, PQ · Execute protocols ...

Overview · Inscríbase sin demora Se espera un gran volumen de solicitantes para el puesto que se detalla a continuación, no espere para enviar su CV. · Validation & Engineering Group, Inc. (V&EG) · a · Pinnaql · company is a leading services supplier who provides solutions for th ...

Job Description: · The ideal candidate will have a Bachelor’s degree in Science with at least 8 years of experience in direct pharmaceutical quality control areas and regulatory operations. · Proficient using MS Windows and Microsoft Office applications · Strong knowledge of cGxP ...

A challenging role awaits Quality Control Scientist to oversee compliance evaluation and technical documentation generation. · About this Job: · Evaluate regulatory adherence across various areas. · Generate comprehensive technical documents. · ...

Project Coordinator · We are seeking a self-sufficient Project Coordinator to support a downstream biologics validation project at a cGMP manufacturing site. · Key Responsibilities:Coordinate project schedules, deliverables, · and communications across multiple equipment vendors, ...

MF Qualification / Computer System Validation (CSV) Scientist · Asegúrese de leer detenidamente la información sobre esta oportunidad antes de presentar su candidatura. · Validation & Engineering Group, Inc. (V&EG) · is a leading services supplier who provides solutions for the P ...

Job Description · The ideal candidate will have a Bachelor's Degree in Science or Engineering, with at least 3 years of relevant experience in the pharmaceutical or biotechnology industries. · Proficiency in English and Spanish is mandatory. · Strong knowledge of cGxP and regulat ...

Validation & Engineering Group, Inc. (V&EG) · ¿Es este el puesto que está buscando? Si es así, siga leyendo para obtener más detalles y no olvide enviar su solicitud hoy mismo. · is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical ...