Research & Development Chemist II/III

Bachem AG•Torrance, CA

5d•$30 - $53

About The Position

The R&D Chemist II/III within the Process Development Group will be responsible for purification, analysis, and isolation of GMP grade peptides under GMP regulations. This work will encompass preparative and analytical chromatography, and lyophilization.

Requirements

Bachelor's degree in chemistry, biochemistry, or bioengineering with a minimum 3 years’ experience or
Master's degree with 1+ year of experience
Hands-on experience in preparative and analytical reversed-phase high performance liquid chromatography (HPLC) and isolation operations in a GMP environment
Hands-on laboratory experience (academic acceptable, industry preferred) in protein or peptide chemistry
Experience in RP-HPLC and ion exchange chromatography
Experience with synthesis and/or purification
Strong knowledge of GMP regulations and ICH guidelines
Good laboratory notebook and data organization skills
Excellent written and oral communication skills
Basic computer knowledge, including Microsoft Word, Excel and PowerPoint
Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment
Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues
Detail oriented with the ability to troubleshoot and resolve problems
Ability to work independently and manage one’s time
Communicate effectively and ability to function well in a team environment

Responsibilities

Perform preparative and analytical reversed-phase high performance liquid chromatography (HPLC) and isolation operations with direction from supervisor
Follow written procedures such as Standard Operating Procedures (SOP) and Batch Production Records (BPR)
Comply with SOP’s in all aspects of the work and follow GMP regulations
With appropriate training, become well-versed in operation of specific chromatography platforms used in the GMP Manufacturing Group
Document accurately purification conditions and yields in the Batch Production Records (BPR)
Work in close cooperation with synthetic chemists to meet project commitments with regard to deliverable timelines, quantity, and quality
Constantly monitor and improve practices by learning from past projects
Ensure that all laboratory safety and housekeeping standards are met