20 publicaciones de empleo destacadas de quality assurance en barcelona, ct (¡Están contratando!)

Quality Assurance Specialist
Galderma —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Inglés
- Oficina
4d
Study Support Assistant
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Seguro dental
- Seguro oftalmológico
Quality Assurance Technician
Centrient Pharmaceuticals Netherlands —Santa Perpètua de Mogoda, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Oficina
Solicitud rápida
Senior Quality Assurance Engineer (m/f/d)
Ververica GmbH —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Azure
- Java
- AWS
Solicitud rápida
Customer Care Specialist
Spendesk —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Oficina
4d
CX Quality Assurance Lead (Hybrid)
eDreams ODIGEO —Barcelona, Barcelona provincia
- Oficina
- Project management
- Inteligencia artificial
Quality Assurance Trainee
Ferrer —Sant Cugat del Vallès, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Microsoft Office
- Habilidades organizativas
Quality Assurance Officer (Planta Química)
Interquim SA —Sant Cugat del Vallès, Barcelona provincia
- Trabajo híbrido
- Grado
- APIs
Transversal Quality Assurance Coordinator
EBMT —Barcelona, Barcelona provincia
- De 31.574 € a 34.595 € al año
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
- Microsoft Office
1d
Quality Specialist Launch Team
Ball Corporation —Barcelona, Barcelona provincia
- De 62.300 € a 89.690 € al año
- Trabajo híbrido
- Inglés
- Grado
- Manufactura
- Seguro de vida
- Plan de pensiones
Solicitud rápida
QA SPECIALIST - BARCELONA - FINTECH
Adaptive Financial Consulting —Barcelona, Barcelona provincia
- Trabajo híbrido
- Español
- DevOps
- Inglés
- Plan de pensiones
Solicitud rápida
11d
Business Analyst
Product Madness —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Word
- Microsoft Excel
- Oficina
Senior Software Quality Assurance Specialist (Automation Testing) m/f/d
PPG —Barcelona, Barcelona provincia
- Jornada completa
- Azure
- Informática
- DevOps
Solicitud rápida
TECHNICAL DRUG SAFETY OFFICER
Instituto Grifols SA —Sant Cugat del Vallès, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Excel
- Inglés
- Máster
Hybrid role for a Scrum Master and QA
BCome —Barcelona, Barcelona provincia
- Grado
- Control de calidad
- Desarrollo de software
Corporate Quality Specialist
Grifols SA —Sant Cugat del Vallès, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
- Habilidades de comunicación
Quality Engineer
Thales —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Oportunidades de crecimiento y desarrollo profesional
- Seguro de vida
Customer Service Agent (ES + EN)
Exoticca —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- CRM software
- Español
- Servicio al cliente
Solicitud rápida
Associate - Windows Administrator
Shipco IT —Barcelona, Barcelona provincia
- Jornada completa
- Azure
- Informática
- Oficina
Solicitud rápida
Quality Manager
Uriach Italy —Sant Cugat del Vallès, Barcelona provincia
- Español
- Microsoft Excel
- Inglés
Solicitud rápida

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Quality Assurance Specialist

Galderma -
Barcelona, Barcelona provincia

Solicitar ahora

Detalles del empleo

Jornada completa
Hace 4 días

Cualificaciones

ESO
Biología
Microsoft Excel
Inglés
Máster
Grado
Farmacia
Química
Relaciones Laborales
Manufactura

Descripción completa del empleo

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.

Further supporting our growth and innovation momentum, we are establishing a new Global Capability Center in Barcelona to deploy new capabilities to effectively support its global commercial and functional teams. Located in the upscale Eixample District in the heart of Barcelona, Galderma’s Global Capability Center offers numerous possibilities for professional development such as exposure to global and cross-functional projects and access to global career opportunities.

We are currently seeking a dynamic and experienced Quality Assurance (QA) Specialist with 3-8 years of experience in the medical device or pharmaceutical industry. The ideal candidate will have expertise in various QA functions, including complaint management, release activities, sterile production, documentation and regulatory compliance. The position is within the External Supplier Organization (ESO) for Sterile Products and You will work closely with ESO suppliers.

Key Responsibilities:

Quality Systems: Contribute to the development, implementation, and maintenance of robust quality systems, including complaint management, deviation management, change control, CAPA, and risk management processes. Main responsibilities for QMS will be complaint management.

Release Activities: Execute product release activities in compliance with regulatory requirements and company standards. Ensure timely and accurate release of pharmaceutical products for distribution.

Sterile Production: Provide QA oversight for sterile manufacturing operations, including aseptic processing, sterilization processes, and environmental monitoring. Ensure adherence to cGMP guidelines, regulatory standards and applicable ISO standards.

Documentation Management: Manage and review quality documentation, including batch records, standard operating procedures (SOPs), risk management, validation protocols, and reports. Ensure documentation complies with regulatory requirements, ISO13485, MDR and internal quality standards.

Regulatory Compliance: Stay abreast of regulatory requirements and industry best practices related to quality assurance. Ensure compliance with FDA regulations, international standards such as applicable ISO standards, and company policies.

Audits and Inspections: Support internal and external audits and regulatory inspections. Support Due Diligence audits for initial qualification of suppliers. Prepare and review audit documentation, respond to audit findings, and implement corrective and preventive actions as necessary.

Continuous Improvement: Identify opportunities for process improvement and quality enhancement. Participate in quality improvement initiatives and projects to optimize quality systems and operational efficiency.

Required Qualifications:

Bachelor's degree in Pharmacy, Chemistry, Biology, or related field.
5-8 years of experience in a quality assurance role within the medical device, pharmaceutical or regulated industry.
Fluency in written and verbal English, any other language is an asset.
Strong operational knowledge of medical device or pharmaceutical manufacturing processes, including production of sterile biological drugs, terminally sterilized and/or aseptically filled products.
Proficiency in documentation management.
Familiarity with regulatory requirements, including cGMP, FDA regulations, ISO13485 & MDR and international guidelines.
Excellent communication
Ability to work independently and collaboratively in a dynamic, fast-paced environment.

Preferred Qualifications

Pharmacist or Master’s degree in Biology, Biotechnology, Biochemistry, Chemistry, Engineering, Microbiology, Life Science or another relevant scientific or engineering discipline.
Previous experience in reviewing supply agreements and manage quality agreements
Previous experience in leading or participating in regulatory inspections and audits.
Problem-solving, and decision-making skills.

Join us in this dynamic role where resilience, strong management, and team-building skills thrive. Your pivotal role as an experienced QA specialist will contributing significantly to Galderma's growth. Apply now for a transformative journey!

What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.

In ESO organization nearly 60 employees work together in a global environment on our world leading brands such as Nemluvio and Sculptra.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged.

We are based in modern offices and located in several places in Europe, such as Barcelona, Alby (France) and Uppsala (Sweden). ESO/API suppliers is located across the Globe and travel is part of the position.

Next steps

We welcome your application via our company website CAREERS Galderma and as soon as possible. The selection process is ongoing and the role may be filled prior the last application date.

If your profile is a match, we will invite you for a first virtual conversation with the recruiter
The next step is a virtual conversation with the hiring manager.
The second step is an interview with SRT Director.
The final step is an interview with Head of Global Supply.

Our people make a difference

At Galderma, you’ll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

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quality assurance empleos en barcelona, ct

Quality Assurance Specialist

Study Support Assistant

Quality Assurance Technician

Senior Quality Assurance Engineer (m/f/d)

Customer Care Specialist

CX Quality Assurance Lead (Hybrid)

Quality Assurance Trainee

Quality Assurance Officer (Planta Química)

Transversal Quality Assurance Coordinator

Quality Specialist Launch Team

QA SPECIALIST - BARCELONA - FINTECH

Business Analyst

Senior Software Quality Assurance Specialist (Automation Testing) m/f/d

TECHNICAL DRUG SAFETY OFFICER

Hybrid role for a Scrum Master and QA

Corporate Quality Specialist

Quality Engineer

Customer Service Agent (ES + EN)

Associate - Windows Administrator

Quality Manager

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