Scientist II

Location: Ridgefield, CT

Duration: 12 Months

Duties & Responsibilities:

Independently designs and performs analytical methods to measure drug formulations by reverse-phase and size exclusion chromatography under Good Laboratory Practices (GLP) guidelines.

Participate in the development, qualification, and validation of new analytical methods.

Maintains an organized and detailed notebook according to Good Documentation Practices (GDP) guidelines.

Reports and treats data with a high level of integrity and ethics. Present results responsibly at team meetings.

Solid knowledge and understanding of applicable GLP regulations.

Work in a collaborative manner with members of other departments.

Review, approve, write, and revise Standard Operating Procedures (SOPs) and Technical Reports.

Comply with applicable regulation, perform all work in a safe manner; Maintain proper records in accordance with SOPs and polices.

Requirements:

Knowledge and experience in high performance liquid chromatography (HPLC) method development and validation for drug formulation analysis.

Experience with HPLC related software, such as Empower, to execute experiments and analyze data.

Ability to work independently in the lab to prepare reagents, pipette solutions accurately, and operate instruments.

Prior experience working in a GxP environment is preferred.

Strong laboratory skills with the ability to resolve and advise on technical issues of a moderate scope and develop new skills through on-the-job experiences.

Clear and effective written and verbal communication skills.

Proven problem solving ability.

Master’s Degree from an accredited institution in a related scientific discipline, OR Bachelor’s Degree from an accredited institution with three plus (3 ) years of experience in a related scientific discipline or equivalent experience in related field.