Quality Assurance Specialist
hace 7 días
Galderma is a leading player in the dermatology sector, operating in about 90 countries. We offer a range of top-tier brands and services in the dermatology market, covering Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology. Since our establishment in 1981, we have been committed to improving skin health in collaboration with healthcare professionals. Understanding the importance of healthy skin in our lives, we strive to enhance dermatology for every individual.
We are looking for individuals who prioritize results, embrace learning, and bring positive energy to the table. Our ideal candidates are proactive team players who are passionate about making a difference for consumers, patients, and healthcare professionals. We aim to foster personal growth while meeting business objectives. Diversity is celebrated across our organization, respecting the rights and dignity of all employees.
Join Galderma and be part of our bold mission to lead the global dermatology market. Here, you will have the chance to expand your skills, contribute significantly, and make a direct impact.
As part of our growth strategy, we are establishing a Global Capability Center in Barcelona to support our commercial and functional teams. Situated in the vibrant Eixample District, the center offers opportunities for career development, exposure to global projects, and access to international roles.
Job Title: Quality Assurance Specialist
Location: Hybrid, Barcelona
Job Description
This role involves overseeing and executing product release activities in alignment with regulatory standards. Focused on Sterile Manufacturing Operations, the position includes QA functions related to release activities, sterile production, documentation, data integrity, and regulatory compliance.
Key Responsibilities
- Release Activities: Ensure product release activities comply with regulations and company standards.
- Sterile Production: Provide QA oversight for sterile manufacturing operations.
- Documentation Management: Review and manage quality documentation.
- Data Integrity: Implement controls to ensure data accuracy and reliability.
- Regulatory Compliance: Stay updated on quality assurance regulations.
- Quality Systems: Contribute to maintaining robust quality systems.
- Audits and Inspections: Support internal and external audits.
- Continuous Improvement: Identify opportunities for quality enhancement.
- Proven experience in quality assurance within the pharmaceutical industry.
- Knowledge of pharmaceutical manufacturing processes.
- Proficiency in documentation management and data integrity.
- Familiarity with regulatory standards such as cGMP and FDA regulations.
- Strong communication and problem-solving skills.
- Ability to work independently and collaboratively in a fast-paced environment.
- Previous experience in regulatory inspections and audits.
- A diverse and inclusive work environment.
- Competitive compensation with bonuses and benefits.
- Hybrid work culture.
- Personalized career development opportunities.
- Ownership mentality and growth empowerment.
- Submit your CV in English.
- Initial virtual conversation with Talent Acquisition.
- Virtual interview with the hiring manager.
- Panel interview with the team.
At Galderma, we believe in a diverse and collaborative team. We appreciate the unique contributions of each member, creating a professional and supportive environment for growth and success.
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