Scientist

Scientist Liquid Chromatography

Location: Beerse, Belgium (Onsite)

Duration: 12 months

Hours: 40

Imagine your next project working within the small Molecule Method Development, which  is a department within Discovery and Manufacturing Sciences (DPDS) / Chemical and Pharmaceutical Development and Supply (CPDS). The department is responsible for Small Molecule Method Development, Method Validation, Method Transfer and support. This includes Active Pharmaceutical Ingredients, Drug Products, Chemical Raw Materials, Starting Materials, Intermediates and In-Process Controls from early development through the lifecycle for commercial products. We also provide analytical support for all regulatory filings (CTA/IND, NDA/MAA, Post Approval Submissions), Inspections and investigations. As well as focused analytical base business support for the Small Molecule (SM) R&D and Manufacturing product portfolio. Finally we provide development and implementation of Process Analytical Technology (PAT) / New Innovative Analytical Technology Platforms for Small Molecules and Cleaning Validation.

Role and responsibilities

• You are responsible for the planning, coordination and execution of the analytical experimental work (method development, validation, transfer) the main part of this experimental work focusing on analytical methods for assay/purity, content uniformity, ID, moisture and solvents

• You independently lead multiple assigned projects: establishes priorities, checkpoints, and time frames in line with the project- and team objectives/deliverables

• You will collaborate closely with colleagues from analytical, API and Drug product

  development

• You advise and inform management and stakeholders of technical requirements, about potential scientific challenges and risks, prioritisation or resources conflicts and makes suggestions to resolve or mitigate these

• You initiate ideas to improve the support and efficiency of the analytical method development/validation/transfer activities for the R&D portfolio

• You ensure that applicable guidelines, established operating procedures and

  safety regulations adhering to company work standards are being followed

• You author and review technical reports, protocols and standard operating procedures

• You maintain knowledge of Good Manufacturing Practices (GMP) and ICH Guidelines

how to succeed

A bachelor's degree in Analytical Chemistry, Pharmaceutical Technology, or a related scientific field, along with a minimum of 3 years of experience, is required. If you possess a master's degree, we are open to considering recent graduates or individuals with less experience. Additionally, experience in PLC is essential, and we value candidates who are confident and proactive in expressing their thoughts.

You will also bring:

• In-depth technical knowledge and experience for developing/validating and

  transferring analytical methods in support of the R&D project portfolio with a major focus on techniques such as Liquid Chromatography (UHPLC), Mass Spectrometry (Single Quad) is required.

• Knowledge and/or experience with oligonucleotide/oligopeptide Analytical method development is preferred.

• You can work independently, though you are also an excellent collaborator and like to work in a multidisciplinary, inter departmental and cultural divers’ context

• You can oversee projects in a professional way with respect to deadlines and with a good sense of urgency

• You ensure high scientific quality standards for experiments and take on responsibility for these experiments

• You are a prudent risk-taker, who thinks of innovative and creative solutions

• Fluent In English

Benefits

This role offers a very competitive hourly rate. This contract will run for a minimum of 12 months and has a strong possibility of extending.

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

Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years. As a skilled contractor, you’ll play a key part in the thinking, strategy, dynamism - and impact - of this iconic global healthcare company as they touch the lives of nearly a billion people every day. Contribute to the next healthcare breakthrough with your next project at Johnson & Johnson. 

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. PAYE & Umbrella 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”.