Quality Assurance Advisor – Gothenburg

We are searching for Quality Assurance Advisors to one of our customers in Gothenburg!

Are you interested in a challenging opportunity within the Development Quality function in one of the world’s leading pharmaceutical companies? Our customer is now seeking 1-3 Quality Assurance specialists with GMP focus to the Gothenburg team. The role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the company´s projects in the development phase. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting.

Purpose, Offer and Benefits

The company have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

Your Responsibilities

Typical Accountabilities:

• Responsible for quality Release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
• Providing quality input to Manufacturing, Packaging, Labelling & Distribution activities
• Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
• Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects
• Provide appropriate Quality Assurance input to business improvement projects
• Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working.

The Bigger Picture

Our customer is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world´s most serious diseases. 

We are looking for candidates who are available and ready to take on this upcoming consulting assignment in Gothenburg. 

The advantages of being a consultant are many! Not only do you get to work with interesting companies and try many different tasks. You also get to broaden your network that you can benefit from throughout your future career.

Our Expectations

Requirements – Education and Experience:

• Degree in pharmacy or engineering (specializing in Pharmaceuticals) with at least 3 years´ experience of working within a pharmaceutical GMP environment
• Broad understanding of Quality Systems and GMP and related activities to Investigational Medicinal Product (IMP)
• Comprehensive understanding of the pharmaceutical/drug development process
• Good communicator with experience of interacting effectively across interfaces
• Understanding of Project Management processes
• Fluent in written and spoken English

Desirable for the role if you have experience within a pharmaceutical manufacturing organization and you are capable of making effective decisions and able to demonstrate drive and energy in the role to make a difference.