Scientist

Scientist - Microbiology

Location: Leiden, Netherlands - Hybrid working - 3 days a week on site

Duration: 12 Months

Hours: 40 hours per week - will consider 36 or 32

Imagine your next project contributing to the advancement of pharmaceutical science and driving excellence in a global healthcare company.

The scientist will be part of the Microbiology testing team within the QC department. The scientist will be acting as the scientific responsible person to support the microbiological testing aspects associated with Drug Substance and Drug Product manufacturing. This role is dedicated to a continuous improvement project and involves trouble shooting of microbiological methods, proactively making improvements to test methods to stimulate executional excellence, preparing protocols and reports for ongoing continuous improvement projects. Prepare the planning of resources and equipment for all ongoing activities related to the project. The scientist will report to the (Sr) Manager of the QC Microbiological testing team.

roles and responsibilities.

You will be acting as the scientific responsible person to support the microbiological testing aspects associated with Drug Substance and Drug Product manufacturing.

This will involve:

• The scientist will be part of the Microbiology testing team within the QC department.

• Acting as the scientific responsible person to support the microbiological testing aspects associated with Drug Substance and Drug Product manufacturing.

• Dedicated to a continuous improvement project and involves trouble shooting of microbiological methods.

• Proactively making improvements to test methods to stimulate executional excellence.

• Preparing protocols and reports for ongoing continuous improvement projects.

• Prepare the planning of resources and equipment for all ongoing activities related to the project.

• The scientist will report to the (Sr) Manager of the QC Microbiological testing team.

how to succeed.

You will have extensive experience in the pharmaceutical QC industry with a strong focus on microbiology and method improvement, supported by strong analytical and project management skills.

You will also bring:

• Educational Background: PhD or equivalent in Biochemistry, Microbiology or a related field is required.

• Experience: A minimum of 6 years in the pharmaceutical industry is required, specifically within QC, with a strong emphasis on microbiology. This includes expertise in method development/improvement, method validation and analytical method transfers.

• Regulatory Knowledge: Comprehensive understanding of worldwide regulatory GMP requirements and knowledge of FDA and EU GMP.

• Interpersonal Skills: Strong ability to work independently and in team environments, effectively managing stakeholder relationships and addressing biological testing issues. Asserts personal ideas and opinions using persuasion to influence others.

• Analytical Expertise: You have the ability to critically assess analytical investigation reports and conduct statistical analyses (R studio, minitab Matlab). Familiarity with electronic documents and deviation management systems is desirable.

• Laboratory Experience: Extensive operational experience in a Pharmaceutical QC laboratory, specifically with Drug Substance and Drug Product processes. To be trained in and qualified for the assays that you are SME for and be able to perform investigational testing and train technicians for new methods.

• Technical Proficiency: Strong understanding of analytical technical transfer processes, compliance requirements, and troubleshooting skills. Advanced knowledge of modern methodologies; familiarity with cell cultures, microbiology methods, or compendial methods are a distinct advantage.

• Project Management: Demonstrated project management skills, able to effectively oversee and coordinate multiple projects, LEAN, Greenbelt certification.

• If you are passionate about contributing to the advancement of pharmaceutical science, are driven by excellence, and possess the required skills and qualifications, we invite you to apply for this exciting opportunity!

benefits.

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

you are welcome here.

Johnson & Johnson 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.

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”.