Pharmacovigilance Associate - Data Surveillance

Q-Med AB / Kemiingenjörsjobb / Uppsala
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At Galderma we're unique and we embrace difference.
Whether it's the unique breadth of our integrated offering that covers Aesthetics, Consumer, and Prescription products; or our commitment to recognising 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: Pharmacovigilance Associate - Data Surveillance

Location: Uppsala, Sweden (on site)

Job description:
You will implement Pharmacovigilance plans, processes and policies related to the collection, assessment and prevention of adverse effects following the use of our marketed or development products and ensuring the quality of PV activities in R&D and Operations projects in accordance with GxP, local and international regulations and guidelines.

Key responsibilities:

*

Reconcile and process high-quality product safety data and analysis to internal and external stakeholders throughout the product life cycle.
*

Implement adverse event management processes and databases.
*

Implement and execute pharmacovigilance programs and policies with rapid identification and analysis of safety signals to define emerging product safety profiles of all product types and drive patient risk management.
*

Align and implement Pharmacovigilance plans and activities to provide integrated strategic safety expertise and safety deliverables to clinical development programs.
*

Prepare department quality documents and participate in quality audits and inspections



Skills & Qualifications

*

Master's or Bachelors' degree in Life Sciences or equivalent
*

Minimum of 2 years' experience in Pharmacovigilance
*

Good knowledge of ICSR management and of AE and coding conventions (MedDRA, WHO-DD) from the pharmaceutical/medical device industry.
*

Some knowledge of international PV regulations, standards and principles for drugs, cosmetics and/or medical devices.
*

Fluent in English written and oral.



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 the selection process is ongoing.

* 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
* 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.

Ersättning
Not Specified

Så ansöker du
Sista dag att ansöka är 2024-02-01
Klicka på denna länk för att göra din ansökan

Arbetsgivarens referens
Arbetsgivarens referens för detta jobb är "JR008095".

Omfattning
Detta är ett heltidsjobb.

Arbetsgivare
Q-Med AB (org.nr 556258-6882)

Arbetsplats
Galderma

Kontakt
Galderma
mathilda.ostensson@galderma.com

Jobbnummer
8368084

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