Job Information
J&J Family of Companies Associate scientist SMMD in Antwerp, Belgium
Associate scientist SMMD - 2406169484W
Description
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
Primary Location Europe/Middle East/Africa-Belgium-Antwerp-Beerse
Organization Janssen Pharmaceutica N.V. (7555)
Job Function Pharmaceutical Product R&D
Req ID: 2406169484W