Job Summary
We are currently seeking a dedicated QA R&D Chemist I to join our team in Monmouth Junction, New Jersey. This position is crucial for ensuring quality assurance in research and development functions within our organization. The ideal candidate will possess a strong foundation in analytical chemistry and relevant practical experience in a cGMP environment.
Responsibilities
- Conduct quality assurance activities to support research and development projects.
- Perform analytical testing and documentation in accordance with cGMP regulations.
- Collaborate with cross-functional teams to ensure compliance with quality standards.
- Assist in the development and validation of analytical methodologies.
Qualifications
- A Bachelor’s degree in Chemistry or a related scientific discipline with a minimum of 3 years of laboratory experience in a cGMP setting is required.
- Alternatively, a Master’s degree in Chemistry or a related field is acceptable.
- Strong analytical skills and attention to detail.
- Ability to work effectively in a team-oriented environment.
Tris Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
