Scientist

Scientist

Location: Beerse

Contract Duration: 12 months

Hours: Full-time, 40 hours per week

Working mode: On-site (opportunity to work occasionally from home)

Languages: English and Dutch preferred

Pay rate range: Competitive hourly rate

Department Description 

Dissolution Sciences is part of the Global Analytical Development organization within the Therapeutics Development & Supply (TDS) - Synthetics. We develop end to end dissolution and in vitro release methods for immediate, modified, and targeted release formulations for oral, parenteral, and other administration routes. We investigate, characterize, and predict in vitro release rates in standard and biorelevant dissolution media. We validate and transfer dissolution methods, and we investigate deviating dissolution profiles to improve our methods and drug products. We provide (non-) clinical release and manufacturing / characterization support for drug products and build up scientific understanding of the corresponding stability behaviours to enable drug product development. 

Position Overview

We are looking for a Scientist in the Dissolution Sciences team who will play a pivotal role in ensuring the highest quality standards. The successful candidate will improve compliance across the portfolio, steer and coordinate quality investigations, support inspections, and ensure all processes align with GMP regulations.

The position will be performed out of the Beerse campus in Belgium.

roles and responsibilities

• Strengthen compliance in the laboratory by applying phase-appropriate GMP.

• Steer and coordinate Quality Investigations by identifying root causes, implementing corrective actions, and preventing recurrence. Guide the team in writing investigations, documenting observations, and conducting risk assessments to ensure a transparent process.

• Own change control / change management related activities.

• Support internal and external inspections by preparing documentation, guiding inspectors, and answering questions.

• Act as an SME for compliance-related topics, provide advice, stay updated with regulations, and share knowledge with the team.

• Partner with QA to guarantee all processes, follow relevant GMP regulations, coordinate quality checks and implement improvements.

• Represent the team in cross-functional quality workgroups.

• Take up other tasks where appropriate, related to for e.g. lab organization, equipment installation and/or qualification, automation, EH&S.

how to succeed

Qualifications

A Master’s or a bachelor’s degree in Pharmaceutical, Chemistry, or any related sciences. 

Industry experience is preferred.

Competencies & Knowledge

• Knowledge of pharmaceutical sciences relevant to the development of small molecule formulations and analytical chemistry

• Knowledge of cGMP regulations.

• Experience with dissolution testing is a plus.

• Flexible and able to adapt quickly to constantly evolving business needs.

• Open-minded, with ability to work together as one team in a global environment.

• Fast learner with scientific curiosity, self-steering, pro-active and creative.

• Good written and verbal communication skills in Dutch and English. 

• Ability to present clearly and concisely.

benefits

This role offers a very competitive hourly rate. This contract will run for 12 months initially.

you are welcome here

Johnson & Johnson Innovative Medicine is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

about Johnson & Johnson Innovative Medicine

Patients inform and inspire our science-based innovations, which continue to change and save lives. Applying rigorous science and compassion, we confidently address some of the most complex diseases of our time and unlock the potential medicines of tomorrow.

Our diverse portfolio spans multiple therapeutic areas — Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina.

We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way.

application process

We are looking to process the first round of applications within the next 2 working days.

We do not accept applications via email. The pay rate for this role will depend on how you are paid. Options are available. 

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.