Renaissance LLC

All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.


Overview

The purpose of the Scientist I, QC Spray/Particulate role is to perform basic tests and analysis and conduct laboratory procedures in compliance with established protocols under supervision, while provide administrative support to ensure an efficient operation of the laboratory. This role will keep records and provide information to others. The role will maintain a level of appropriate scientific knowledge in assigned area and perform scientific literature searches and evaluations as required, while understanding and complying with accepted laboratory and safety procedures.

Hours are 3:00 pm to 11:30 pm

Responsibilities

• File, scan, organize and upload scientific documents.

• Obtain approvals on documentation when necessary.

• This role may be asked to contact vendors (e.g. to obtain price quotes and other information).

• Test chemical components or products as assigned. This role involves the use and maintenance of major laboratory instruments and equipment (e.g. HPLC, UPLC, FTIR, HIAC, PLM, Nasal spray test equipment, as well as, wet chemical skills)

• This role may use Renaissance quality systems (e.g. Documentum, LIMs, LN)

• Tests chemical components or products using major laboratory instruments such as HPLC, GC, FTIR, UV-VIS spectrophotometer, pH meter, viscometer, etc.

• Understand and execute protocols and provide information to draft in-house test standards and methods.

• Within area responsibility, understand and comply with all Renaissance safety, environmental and quality practices and procedures as outlined in organizational/departmental guidelines and SOPs, as well as applicable federal, state and local regulations.

• Perform other duties as assigned.

• Work as a team player.

• Flexibility in working hours may be requested - dependent on company need.

Qualifications

• Bachelor of Science Degree in Chemistry, Biology or related science required.


• 0-2 years' experience in cGMP laboratory.

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