Qualified Person

Jobinhalt

Want to be recognized for your leadership? We offer that

Ready to lead a high performing, diverse team? We offer that too

Welcome to AbbVie!

At AbbVie, we offer you the resources and a global reach to empower your innovative mindset. From day one, we’ve known it takes teamwork and collaboration to develop the scientific breakthroughs, innovative pipelines, and therapies that change millions of patients’ lives around the world. In short, we know it takes “you” to make those ground-breaking advancements happen. We take pride in serving and supporting our communities and protecting the environment, making a lasting impact that’s felt within healthcare and beyond.

Odyssea Pharma is a pharmaceutical production and our success is based on the commitment of our teams on the site and around the world. Odyssea Pharma sprl is one of the Abbvie Group’s centers of excellence for women’s health, offering the GMP manufacturing of the Levosert ™ hormonal intrauterine device and a quality and regulatory expertise from a dedicated site located in Liège (Grace-Hollogne), in Belgium.

We are currently recruiting a Qualify Person to be part of our Quality team in our Liège site, Odyssea Pharma, in Belgium , reporting directly to the Head of Quality.

Does this role entice you? Then read on for some of the day-to-day responsibilities:

You will

• Ensure that finished goods releases finished are made efficiently, on time and in compliance with regulatory requirements
• Issuing certificates of conformity
• Support the implementation and maintenance of the QMS in line with corporate and regulatory requirements
• Supervise all GxP processes applicable to the Odyssea site
• Ensure the resolution of quality events (deviations, OOS...) and facilitate the implementation of CAPA
• Act as a quality representative during inspections and audits
• Participate actively in the internal audit program
• Actively participate in process simplification and continuous improvement efforts
• Support the RA requests from Marketing Authorization Holders
• Manage documentation related to activities above, including the alignment between RA files from MAHs and local specifications/instructions as well as the data integrity dimension
  
  

Job Classification

Experienced

Job

Quality Assurance

Primary Location

WEC-Belgium-Liège

Organization

Operations

Schedule

Full-time

Travel

No

Want to be recognized for your leadership? We offer that

Ready to lead a high performing, diverse team? We offer that too

Welcome to AbbVie!

At AbbVie, we offer you the resources and a global reach to empower your innovative mindset. From day one, we’ve known it takes teamwork and collaboration to develop the scientific breakthroughs, innovative pipelines, and therapies that change millions of patients’ lives around the world. In short, we know it takes “you” to make those ground-breaking advancements happen. We take pride in serving and supporting our communities and protecting the environment, making a lasting impact that’s felt within healthcare and beyond.

Odyssea Pharma is a pharmaceutical production and our success is based on the commitment of our teams on the site and around the world. Odyssea Pharma sprl is one of the Abbvie Group’s centers of excellence for women’s health, offering the GMP manufacturing of the Levosert ™ hormonal intrauterine device and a quality and regulatory expertise from a dedicated site located in Liège (Grace-Hollogne), in Belgium.

We are currently recruiting a Qualify Person to be part of our Quality team in our Liège site, Odyssea Pharma, in Belgium , reporting directly to the Head of Quality.

Does this role entice you? Then read on for some of the day-to-day responsibilities:

You will

• Ensure that finished goods releases finished are made efficiently, on time and in compliance with regulatory requirements
• Issuing certificates of conformity
• Support the implementation and maintenance of the QMS in line with corporate and regulatory requirements
• Supervise all GxP processes applicable to the Odyssea site
• Ensure the resolution of quality events (deviations, OOS...) and facilitate the implementation of CAPA
• Act as a quality representative during inspections and audits
• Participate actively in the internal audit program
• Actively participate in process simplification and continuous improvement efforts
• Support the RA requests from Marketing Authorization Holders
• Manage documentation related to activities above, including the alignment between RA files from MAHs and local specifications/instructions as well as the data integrity dimension