Ra and Quality Responsible Person Pt

2 semanas atrás

Lisboa, Portugal Galderma Tempo inteiro

With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that spans the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermo-cosmetics, 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’re 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.

Job Title: RA and Quality responsible

Location: Lisbon

Key Responsibilities:
- Registration of new drug products, cosmetics and medical devices and maintenance of registered products in order to ensure viability of these products in the marketplace.- Ensure compliance with Galderma policies and procedures with respect to regulatory and give support to all departments within this scope.- Handle questions/querys from local Autorithies.- Maintain registration status of medicinal products.- Management of compliance activities.- Manage quality and quality compliance activities (including management of quality complaints and CAPA, establishement of a QMS, give support to local recalls, give support to Inspections & Audits).- Ensure qualification and audit status of local manufacturing (CMO), wholesaler (LSPs and repackagers

Skills & Qualifications:
- Degree in Pharmacy / Pharmaceutical Sciences- Experience in Regulatory/Quality Affairs- Experience in communication with the health authorities- Good pharmaceutical background- Understands the organizational structure and adapts behaviour accordingly.

What we offer in return- You will be working for an organization that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.- You will receive a competitive compensation package with bonus structure and extended benefit package.- You will be able to work in a hybrid work culture.- You will participate in feedback Loops, during which a personalized career path will be established.- You will be joining a growing company that believes in ownership from day one where everyone is empowered to grow and to take on accountability

Process steps- Send your CV in English- If your profile is a match, we will invite you for a first virtual conversation with Talent Acquisition- The next step is a virtual conversation with the hiring manager.- The final step is a panel conversation with the extended team

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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