QA Supplier Control Specialist

Publiceringsdatum: 2024-12-02

Letar du efter ett jobb inom yrken med teknisk inriktning? Det är nu möjligt för dig att få jobb som kvalitetsingenjör, kemiteknik/kvalitetstekniker, kemiteknik hos Q-Med AB. Q-Med AB behöver någon som vill arbeta heltid. Om du är tillgänglig för tills vidare, ta en titt på denna jobbannons.

Om du redan bor i närheten av Uppsala, är det här din chans att söka ett spännande jobb Q-Med AB söker för närvarande efter ambitiösa individer som vill utvecklas i rollen som kvalitetsingenjör, kemiteknik/kvalitetstekniker, kemiteknik. Kolla in deras ledig tjänst och se om du har vad som krävs för att bli en del av deras team. Du har fortfarande tid att söka jobbet som kvalitetsingenjör, kemiteknik/kvalitetstekniker, kemiteknik hos Q-Med AB om du sickar in din ansökan senast sista ansökningsdag som är måndag den trettionde december 2024.

Jobbannons

Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.

At Galderma, we actively give our teams reasons to believe in our 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: QA Supplier Control Specialist

Location: Uppsala, Sweden (hybrid)

Job Description

Join Galderma as QA Supplier Control Specialist in our supplier control team, where you will have a unique opportunity to work with our suppliers, have an impact on Galderma's QA work and grow in your career!

Key Responsibilities

• Manage supplier control and supplier management.
• Plan and perform quality audits of suppliers, service providers and contract manufacturers.
• Analyse audit data and identify deviations from GMP/GDP and follow up on audit observations.
• Manage supplier change notifications.
• Manage deviations in relation to materials and services.
• Manage quality agreements.
• Research and evaluate QA policies, deploying strategies for improved effectiveness.
• Analyze ongoing QA processes and identify areas for improvement.
• Establish relationships with internal and external stakeholders, advising and guiding on QA matters.

Skills & Qualifications

• Bachelor's/master's degree within a relevant field.
• Documented experience working with GMP within medical devices (ISO 13485) and/or pharmaceuticals is required.
• Professional level in Swedish and English
• Experience from quality or regulatory in a regulated environment is an advantage.
• Experience with supplier management is an advantage.
• Experience from laboratory work is an advantage.
• To succeed in this role, you are collaborative and independent individual with experience, responsibility, and a proactive approach. We value curiosity, adaptability, and a commitment to internal collaboration. Embrace change, drive development, and think innovatively. Join us in shaping our dynamic future!

Other

The role will include occasional travelling to suppliers.

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.

As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure 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 just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.

Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible though no later than the 6th of January of 2025. The selection process will be completed in January.

• If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
• The next step is an interview with the hiring manager and 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.