Specialist, QA

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Site Name: Belgium-Wavre
Posted Date: Mar 23 2021

The purpose of the role is to assure and maintain the organization of the activities linked to the quality oversight of the manufacturing activities in the production building of Shingrix bulk production. By the quality oversight of the manufacturing process and the use of quality systems in place, ensure the quality of the product and the supply of the bulk product in a timely manner

Your Responsibilities

• Represent Quality assurance in the decision linked to the manufacturing activities
• Participate the improvement of the quality systems in the production building to assure compliance of consistency campaign and the commercial production
• Ensure and organize the implementation of quality oversight activities linked to the documentation review (Check-lists, batch-records..)

• Identify, Develop and Implement improvements to the quality oversight processes
• Training and coaching manufacturing on efficient deviation management and risks identification, including facilitating and/or contributing to risk identification workshops or root cause analysis for deviations.
  
  

Why you?

Basic Qualifications

We are looking for professionals with these required skills to achieve our goals:

• University degree: master degree in Sciences/Engineering e.g. Pharmacist / Master in Sciences / Bio Engineer pharmaceutical
• Minimum 5 years in the Pharmaceutical/Biotech industry with significant experience of GMP

• French fluent and professional writing and speaking in English are a must.
• Preferred knowledge of vaccines and/or immunology process and products (manufacturing).
  
  

Preferred Qualifications

If you have the following characteristics it would be a plus:

• Minimum of 1-2 years of experience in manufacturing and/or QA within the pharmaceutical industry.
• Good knowledge of cGMP
• Autonomy
• Good interpersonal and communication skills
• Demonstrated ability of stakeholder management

• Demonstrated experience in influencing improvement activity to ensure implementation of appropriate actions
• Knowledge of primary processes is an asset
  
  

Why GSK?

Our values and expectations are at the heart of everything we do and form an important part of our culture. These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork in a culture of Innovation, Performance and Trust.

GSKVaccines – Our Vaccines business has a broad portfolio and innovative pipeline of vaccines to protect people of all ages. We deliver over two million vaccine doses per day to people living in over 160 countries.

For further information, please visit www.gsk.com.

At GSK we value diversity and treat all candidates equally. We aim to create an inclusive workplace where all employees feel engaged, supportive of one another, and know their work makes an important contribution.

We provide a supportive working environment, and a range of development challenges and opportunities. We also offer competitive benefits and compensation packages designed to attract and to retain the very best.

If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.

Our goal is to be one of the world’s most innovative, best performing and trusted healthcare companies. We believe that we all bring something unique to GSK and when we combine our knowledge, experiences and styles together, the impact is incredible. Come join our adventure at GSK where you will be inspired to do your best work for our patients and consumers. A place where you can be you, feel good and keep growing.

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