Annecy, Auvergne-Rhône-Alpes, France
6 months ago

Job Overview

Job Type
Full-Time
Pay
Not disclosed

Job description

Location:
Annecy, Auvergne-Rhône-Alpes, France
Work arrangement:
On-site

Role Summary

Join us by integrating the 3rd largest pharmaceutical laboratory in the world and a growing site between lake and mountains!

Leader in medical aesthetics, Allergan, a subsidiary of the Abbvie Group, develops and manufactures sterile injectable products based on hyaluronic acid, for the aesthetic treatment of the face, thus contributing to the well-being of patients.

Our ambition? Offering the best innovation in the aesthetic medicine market.

As part of a job creation, we are recruiting for our Quality department, based in our center of excellence for aesthetic medicine in Annecy, Haute-Savoie:

Post-market Quality Assurance Manager on permanent contract

This mission will suit anyone wishing to evolve within a multicultural organization combining agility, commitment and speed of action.

Under the responsibility of the Quality Director, your role will consist of being one of the Site Quality representatives for marketed AbbVie products and the global supply chain with a dedicated team under your responsibility.

In this capacity, you will have the following responsibilities

Act as the primary quality representative for the global supply chain and make product quality decisions in alignment with different stakeholders (local and global)

Supervise and implement the overall post-market surveillance strategy, including the development and analysis of PSURs (Periodic safety update report) and the management of PMCF (Post market Clinical follow up), in order to anticipate risks, identify levers for improvement and guide organizational choices

Oversee and implement the overall complaints management strategy and review of market signals by reinforcing a proactive approach to anticipate and evaluate customer satisfaction

Supervise and implement the Supplier Quality strategy in order to select, evaluate and develop high-performance partners to meet our challenges of excellence, innovation and compliance with standards

Be responsible for implementing and maintaining the effectiveness of the quality system through the application and maintenance of quality policies, procedures and systems within its scope

Ensure coordination of activities related to major Quality events, ensuring alignment and engagement of global stakeholders and their involvement around key decisions

  • Ensure the management of stability programs, integrate and promote the data collected and guide actions to guarantee the reliability and durability of products
  • Manage the implementation of trend reviews, issue Quality recommendations supporting the vision and mission of AbbVie Quality
  • Ensure audits, monitoring of KPIs and deployment of action plans
  • Establish and manage the budget for your department

Ensure the management of a multidisciplinary quality team. Engage and mobilize your team around a collaborative dynamic of teamwork, performance and ownership.

Requirements

You have the assets to join us

  • Higher scientific training (BAC+5 required) or a pharmacist diploma.
  • A minimum of 10 years of experience managing quality assurance, regulatory, operations or technical support operations in a pharmaceutical environment.
  • Knowledge of FDA, ISO13485 requirements for medical or pharmaceutical devices.
  • Common use of English (spoken and written).
  • Strong knowledge of quality assurance/control, manufacturing, laboratory, technical support, regulatory and/or validation is required.
  • You demonstrate leadership and have the necessary skills for management and team supervision.
  • Relational ease and an ability to communicate both written and orally at all levels of the organization
  • You have the ability to synthesize information and present it.
  • You have a sense of analysis and problem solving,
  • You know how to manage several complex tasks simultaneously and act as a leader and member of a team
  • An ability to manage complexity, influence and be adaptable to change

Benefits

AbbVie is an equal opportunity employer committed to acting with integrity, driving innovation, transforming lives and serving our community. Equal opportunity employer for veterans and people with disabilities.

About the Company

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Role:
Post Market Quality Assurance Manager M/F
Industry Type:
Pharmaceuticals
Job Type:
Full-Time

Company profile

AbbVie Inc. is an American pharmaceutical company headquartered in North Chicago, Illinois. It produces drugs to treat a wide range of medical issues. The company ranks sixth on the list of largest biomedical companies by revenue, 77th on the Fortune 500 and 108th on the Forbes Global 2000. Its name combines Abbott, the name of its former parent company, with vie, intended as a reference to a Latin root meaning life.

Company Size
50,000 - 100,000 employees
Headquarters
North Chicago, Illinois, United States
Founded
2012
Funding Stage
Public

More jobs at AbbVie

Similar QA Engineer jobs at other companies