Associate Scientist Smmd

il y a 3 semaines


Beerse, Belgique Johnson & Johnson Temps plein

**Associate Scientist SMMD**

**limited J&J contract**

**Job description**
- Responsible for the coordination and execution of the analytical work (method development, -validation, -transfer) to be done in support of assigned projects and tasks, with a primary focus on the relevant quality attributes of the active pharmaceutical ingredients (API’s), drug products (DP’s) as well as raw materials/intermediates, and this using a variety of analytical techniques, such as Liquid chromatography, Gas chromatography, Titrations and KF water determinations.
- Manages multiple assigned projects and tasks, while establishing the right priorities in line with project/customer requirements and agreed timelines.
- Informs supervisor about potential technical/scientific challenges and risks, prioritization or resources conflicts.
- Reviews the scientific data and assists the AD-SMMD scientists in summarizing/interpreting the data and in drawing conclusions.
- Responsible for GMP documentation of generated data and protocol/report writing.
- Ensures that applicable guidelines, established operating procedures and safety regulations adhering to company work standards are being followed.
- Review, interpretation and reporting of the obtained analytical data.
- Works closely with the scientists of AD-SMMD and other partner departments to ensure fit for purpose analytical work and reporting.

**Qualifications**:
Education & experience
- You hold a Master’s degree with at least 2 years of relevant experience in chromatographic (UHPLC, HPLC, GC, Titrations and KF water determinations) method development and validation.
- In-depth knowledge and experience in GMP regulations and working in a GMP environment.
- Profound technical knowledge and proficiency of different (instrumental) analytical techniques, i.e., UHPLC/HPLC, GC, titration etc., including data handling systems, preferably Empower 3 and OpenLab.
- Knowledge and experience in analytical report writing using electronic document management systems.
- Previous experience with working in a global and/or matrix organization. Experience in collaborating with external partners, e.g., contract research organizations, is considered a plus.

Competencies
- Project management
- Prudent risk-taking
- Self-awareness & adaptability
- Ensure high scientific quality standards for experiments and take on responsibility for these experiments.
- Efficient, flexible and dynamic
- Innovative mindset - Problem solver
- Results and performance driven
- Sense of urgency
- Excellent communication skills (verbally and written)
- Excellent English oral and written proficiency.
- You are able to work independently and within a team, but also inter-departmental while embracing cultural diversity


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