Quality Assurance Specialist

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 bodys 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.

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 Galdermas 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:

• Bachelors 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 Masters 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 Galdermas 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 youll 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.