Post-Doc (Research Associate/Fellow) Analytical Development Small Molecule Method Development-00000TW6
Description
Janssen Research and Development (Janssen R&D) of the Janssen Pharmaceutical Companies of Johnson & Johnson, Small Molecule Method Development/Analytical Development (AD-SMMD) has a Post-Doc vacancy (1 year) in Beerse, Belgium.
This vacancy is an ideal opportunity to obtain applied pharmaceutical analytical industrial experience.
Janssen Pharmaceutical Companies of Johnson & Johnson develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease, diabetes, hematology, metabolic disorders, immunologic disorders, and reproductive medicine.
AD-SMMD is a department of Pharmaceutical Development and Manufacturing Sciences (PDMS) within the Janssen R&D organization.
The department is responsible for the analytical method development/validation of assay and related compounds evaluation/characterization test methods of small molecule drug substance, drug product, intermediates, chemical raw materials and in-process controls from early development through the lifecycle for commercial products; analytical transfer of these methods to internal and/or external clinical and commercial testing sites; characterization, certification, management and distribution of small molecule reference standards; supporting all regulatory filings (CTA/IND, NDA/MAA, post approval submissions), inspections and investigations.
Description of the role/key areas of accountability:
• The Scientist–Post-Doc will be responsible for method development and validation including HPLC, UHPLC, GC and wet-chemistry tests with regard to assay/related compounds and other relevant attribute tests of small molecule active pharmaceutical ingredients (API’s) and its raw materials/intermediate products and pharmaceutical finished products (DP’s).
• Designs, executes scientific experiments, will originate and defend experimental protocols.
• Applies state-of-the-art scientific knowledge to assigned projects; show a high level of technical proficiency in separation sciences and demonstrate reasonable knowledge/expertise outside of own field. This individual will introduce new techniques to the solution of technical problems.
• Keeps abreast of current scientific developments and new techniques by reading the current scientific literature and by interacting with colleagues. Applies information from literature searches to current projects, and to the development of new ideas.
• Works independently under general guidance on the assigned projects. Actively and personally involved in lab work.
• Interacts with other departments and project teams, presents results in meetings as appropriate to support team and departmental goals.
• Establishes priorities, checkpoints, and time frames for experimental work in support of individual and project / team objectives.
• Is responsible for the safe use of equipment, proper recording of information and raw data obtained during the experiments and for the timely preparation of technical reports through use of electronic laboratory notebook systems and electronic document management systems. Summarizes, interprets, reviews data, and draws conclusions. Ensures that records are properly retained.
• Follows established operating procedures and safety regulations adhering to company work standards.
Qualifications
Qualifications and Critical Experience Required:
• Advanced scientific degree (PhD) in chemistry or pharmaceutical chemistry/sciences with specialization in analytical chemistry.
• Thorough technical/analytical chemistry knowledge and high level of proficiency of different separation techniques (e.g. LC (UHPLC), GC) are required.
• Knowledge of wet chemistry techniques (e.g. titrations, specific optical rotation) is a plus.
• Knowledge of chromatographic software such as Waters Empower is preferred. Working knowledge of Waters and/or Agilent chromatographic instruments is preferred.
• Excellent interpersonal and communication skills are required.
• Excellent English oral and written proficiency is required.
Critical Competencies:
• Collaboration and Teaming
• Problem Solving
• Results and Performance Driven
• Sense of Urgency
• Self Awareness & Adaptability
Primary Location:
Belgium-Beerse
Primary Location:Europe/Middle East/Africa-Belgium-Antwerp-Beerse
Organization: Janssen Pharmaceutica N.V. (7555)
Job Function: R&D
Description
Janssen Research and Development (Janssen R&D) of the Janssen Pharmaceutical Companies of Johnson & Johnson, Small Molecule Method Development/Analytical Development (AD-SMMD) has a Post-Doc vacancy (1 year) in Beerse, Belgium.
This vacancy is an ideal opportunity to obtain applied pharmaceutical analytical industrial experience.
Janssen Pharmaceutical Companies of Johnson & Johnson develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease, diabetes, hematology, metabolic disorders, immunologic disorders, and reproductive medicine.
AD-SMMD is a department of Pharmaceutical Development and Manufacturing Sciences (PDMS) within the Janssen R&D organization.
The department is responsible for the analytical method development/validation of assay and related compounds evaluation/characterization test methods of small molecule drug substance, drug product, intermediates, chemical raw materials and in-process controls from early development through the lifecycle for commercial products; analytical transfer of these methods to internal and/or external clinical and commercial testing sites; characterization, certification, management and distribution of small molecule reference standards; supporting all regulatory filings (CTA/IND, NDA/MAA, post approval submissions), inspections and investigations.
Description of the role/key areas of accountability:
• The Scientist–Post-Doc will be responsible for method development and validation including HPLC, UHPLC, GC and wet-chemistry tests with regard to assay/related compounds and other relevant attribute tests of small molecule active pharmaceutical ingredients (API’s) and its raw materials/intermediate products and pharmaceutical finished products (DP’s).
• Designs, executes scientific experiments, will originate and defend experimental protocols.
• Applies state-of-the-art scientific knowledge to assigned projects; show a high level of technical proficiency in separation sciences and demonstrate reasonable knowledge/expertise outside of own field. This individual will introduce new techniques to the solution of technical problems.
• Keeps abreast of current scientific developments and new techniques by reading the current scientific literature and by interacting with colleagues. Applies information from literature searches to current projects, and to the development of new ideas.
• Works independently under general guidance on the assigned projects. Actively and personally involved in lab work.
• Interacts with other departments and project teams, presents results in meetings as appropriate to support team and departmental goals.
• Establishes priorities, checkpoints, and time frames for experimental work in support of individual and project / team objectives.
• Is responsible for the safe use of equipment, proper recording of information and raw data obtained during the experiments and for the timely preparation of technical reports through use of electronic laboratory notebook systems and electronic document management systems. Summarizes, interprets, reviews data, and draws conclusions. Ensures that records are properly retained.
• Follows established operating procedures and safety regulations adhering to company work standards.
Qualifications
Qualifications and Critical Experience Required:
• Advanced scientific degree (PhD) in chemistry or pharmaceutical chemistry/sciences with specialization in analytical chemistry.
• Thorough technical/analytical chemistry knowledge and high level of proficiency of different separation techniques (e.g. LC (UHPLC), GC) are required.
• Knowledge of wet chemistry techniques (e.g. titrations, specific optical rotation) is a plus.
• Knowledge of chromatographic software such as Waters Empower is preferred. Working knowledge of Waters and/or Agilent chromatographic instruments is preferred.
• Excellent interpersonal and communication skills are required.
• Excellent English oral and written proficiency is required.
Critical Competencies:
• Collaboration and Teaming
• Problem Solving
• Results and Performance Driven
• Sense of Urgency
• Self Awareness & Adaptability
Primary Location:
Belgium-Beerse
Primary Location:Europe/Middle East/Africa-Belgium-Antwerp-Beerse
Organization: Janssen Pharmaceutica N.V. (7555)
Job Function: R&D