Quality Assurance Specialist - Biologics 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.
We understand that the skin shapes our lives, and 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.
Job Title: Quality Assurance Specialist - Biologics Location: Hybrid, Barcelona Job Description: This person will oversee and execute product release activities in compliance with regulatory requirements and global standards.
The main scope of this position will cover Sterile Manufacturing Operations, collaborating with expertise in QA functions, including release activities, sterile production, documentation, data integrity, and regulatory compliance.
Key Responsibilities: Release Activities: Oversee and execute product release activities in compliance with regulatory requirements and company standards.
Sterile Production: Provide QA oversight for sterile manufacturing operations, including aseptic processing, sterilization processes, and environmental monitoring.
Documentation Management: Manage and review quality documentation, including batch records, standard operating procedures (SOPs), validation protocols, and reports.
Data Integrity: Implement and maintain data integrity controls to ensure the accuracy, completeness, and reliability of quality data.
Regulatory Compliance: Stay abreast of regulatory requirements and industry best practices related to quality assurance.
Quality Systems: Contribute to the development, implementation, and maintenance of robust quality systems, including deviation management, change control, CAPA, and risk management processes.
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