Drug Product Development Leader - Mechelen, BE

Job description

Pleased to meet you, we are Galapagos, a dynamic fast growing Biotech company with offices in Europe in Belgium (Mechelen), France (Romainville), the Netherlands (Leiden), Basel (Switzerland), Italy, Spain, Germany, UK and in the US (Boston).

We’re in the business of changing lives. In our quest to discover and develop life-improving medicines we go where no one has ever gone before. In every challenge we face, we see new opportunities. We want to challenge the impossible. We need thought leaders and rapid thinkers, entrepreneurs in spirit and status quo-fighters. Collaborative innovators and perseverant idealists. We need the best-in-class. In other words, we need you.

We are looking for a Drug Product Development Leader

Scope of the job

The core purpose of the job is to manage the drug product development and clinical bulk supplies for various development projects.

As an expert member of the CMC group, you will provide drug product development expertise to several development projects. Highly qualified in pharmaceutical technology, you will come up with formulation and production strategies needed to support early development projects.

Your role

As Drug Product (DP) Development Leader within CMC, you are responsible for the drug product development and bulk supply strategy and execution thereof according to the CMC - and clinical plan for various development projects. You report into the Head of Drug Product Development.

This includes: 

• Working in the CMC development team on a project basis, together with a Drug Substance Development Leader, an Analytical Development Leader, a Clinical Supplies Leader and a CMC Dossier Leader. You will have frequent interaction with other CMC team members to build the early CMC development plan and ensure the Drug Product development activities execution thereof.
• Drug product – formulation development for pre-clinical safety studies and clinical supplies.
• (bulk) Manufacturing of development batches and GMP batches for clinical purposes.
• Evaluation and review of development data (composition/process/PK data) and adjustment of formulation/process as needed.
• Evaluation of stability data in cooperation with Analytical Development Leader and adjust further strategy and plan as needed.
• Preparation, review, approval and appropriate storage / archiving of DP CMC source documents for clinical trial applications (quality section) and prepare responses to regulatory questions.
• Selection (in alignment with Head DP development) and management of External Service Providers executing the drug product development / manufacturing activities.
• Collaboration (in alignment with CMC team when needed) with internal Quality and Compliance department for project related quality topics and to assure that ESPs are performing according to cGMPs.
• Interaction with the CMC project managers in Planning & reporting to provide Drug Product development budget information.
• Ensure the Product Specification File is kept up to date.
• Interaction with other CMC team members to build the CMC development plan and ensure execution thereof.
• Adherence to existing Policies and Procedures and ensure timely completion of relevant training.
• Staying abreast of current and new technologies applicable for drug product development and clinical manufacturing and latest regulations and guidelines.
• Establishing and building important relationships with the Late Discovery group and project team members from development.

Job requirements

Who are you ?

Master of Science (MSc) or PhD in chemistry, pharmaceutical sciences or bio-engineering or equivalent by experience

At least 3 years of relevant experience in a drug product development role

Outstanding verbal and written English language skills required

Ability to actively listen and engage in constructive communication with the different team members

Excellent team player

Strong planning & organisation skills and excellence in supervising projects

Hands-on and pragmatic

What’s in it for you ?

You will be part of a fast growing and amazing company. As ‘make-it-happener’ you will get all the support you need to make your job successful. At Galapagos we aim to recruit the best people, who stand out among their peers, with integrity and excellent interpersonal and organizational skills. Our employees are the strength behind Galapagos, a highly motivated team, eager to maintain Galapagos’ leading position and achieve breakthroughs in pharmaceutical research. Galapagos offers a competitive remuneration package and a dynamic work environment.

We are Galapagos : together we can make it happen…!