Scientist Liquid Chromatography

il y a 4 semaines

Beerse, Belgique Johnson & Johnson Temps plein

**About Johnson & Johnson**:
Small Molecule Method Development is a department within the Global Analytical Development department in the Therapeutics Development and Supply (TDS) organization within Johnson & Johnson Innovative Medicine R&D. 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 Synthetics R&D and Manufacturing product portfolio. Finally, we provide development and implementation of Process Analytical Technology (PAT) / New Innovative Analytical Technology Platforms for Synthetics and Cleaning Validation.

In the SMMD department in Beerse, Belgium, we are currently looking for a

**Scientist - Liquid Chromatography Method and Product developer**

**Key Responsibilities**:

- Design and implement the scientific product characterization strategy of peptides in close collaboration with the clinical release & stability organization.
- Planning, coordination and execution of the analytical experimental work, i.e. method development, validation and transfer to support initial product characterization.
- Perform analysis in support of product characterization and clinical development. Focus will be on Liquid Chromatography.
- Perform scientific data aggregation and evaluation, communicate and discuss your results with the project team.
- Digitalization of analytical data sets to drive analytical data sciences.
- Ensure that applicable guidelines, established operating procedures and safety regulations adhering to company work standards are being followed.
- Author and review technical reports, protocols and standard operating procedures.
- Maintain knowledge of Good Manufacturing Practices (GMP) and ICH Guidelines.

**Qualifications**:
**Education**:

- You hold mínimally a PhD or Master degree in Chemistry or Pharmaceutical Sciences or related science with at least 3 years of relevant experience.

**Experience and Skills**:
**Required**:

- In-depth technical knowledge and experience for developing/validating and transferring analytical methods in support of the R&D project portfolio with major focus on Liquid Chromatography (UHPLC) is required.
- Knowledge and/or experience with Synthetics 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.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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