Today
Unspecified
Mid Level Career (5+ yrs experience)
$90,000
No Traveling
Engineering - Chemical
Andover, MA (On/Off-Site)
Energy Storage company is commercializing a new class of flow battery technology for low-cost grid-scale energy storage based on novel aqueous electrolyte solutions. We are seeking a quality control professional from the chemicals, pharmaceutical, or biotech industries to assist in the analysis and verification of a range of flow battery electrolyte samples. Typical analytical testing will comprise HPLC, ICP, UV-Vis, viscometry, turbidity, and conductivity analyses. This role will provide critical chemical quality information to assist in the development of new battery electrolyte products, in the development of manufacturing processes with manufacturing partners, and in the quality control of commercial electrolyte products. The successful candidate will interface with a staff of senior analytical chemists, battery scientists and chemicals manufacturing supply chain partners to ensure that the battery electrolyte under development and in the field meets or exceeds product specification. The candidate selected for role will be joining a team that currently has 4 members, supporting QC analysis of electrolytes, generating data, and testing samples from Research and Development product development.
Basic Required Qualifications:
• Completion of a BS degree in a scientific discipline with laboratory experience
• 1 year or more of relevant work experience in a laboratory environment: research, commercialization of a chemical, pharmaceutical or biotech product
• Experience with state-of-the-art analytical chemistry techniques (e.g. high performance liquid chromatogram (HPLC) and/ or inductively coupled plasma optical emission spectroscopy (ICP-OES))
• Able to conduct testing, analyze data, and contribute to planning for next steps
• Demonstrate troubleshooting skills
• Ability to work independently and as part of a team
• The individual must be flexible, able to adapt to a fast-paced, dynamic work environment
• Strong organizational skills with ability to execute parallel projects
• Dependability and timeliness
Desired skills:
• Experience (4+ years) in industrial chemical and/or pharmaceutical product development and quality control
• Experience in analytical method development and validation
• Experience in developing procedures for validation, verification, and periodic monitoring of chemical products to ensure that it meets customer specification
Schedule-4x10 first shift-core hours are from 10am-2pm. Most team members work 8am-6pm, but hours are flexible.
Basic Required Qualifications:
• Completion of a BS degree in a scientific discipline with laboratory experience
• 1 year or more of relevant work experience in a laboratory environment: research, commercialization of a chemical, pharmaceutical or biotech product
• Experience with state-of-the-art analytical chemistry techniques (e.g. high performance liquid chromatogram (HPLC) and/ or inductively coupled plasma optical emission spectroscopy (ICP-OES))
• Able to conduct testing, analyze data, and contribute to planning for next steps
• Demonstrate troubleshooting skills
• Ability to work independently and as part of a team
• The individual must be flexible, able to adapt to a fast-paced, dynamic work environment
• Strong organizational skills with ability to execute parallel projects
• Dependability and timeliness
Desired skills:
• Experience (4+ years) in industrial chemical and/or pharmaceutical product development and quality control
• Experience in analytical method development and validation
• Experience in developing procedures for validation, verification, and periodic monitoring of chemical products to ensure that it meets customer specification
Schedule-4x10 first shift-core hours are from 10am-2pm. Most team members work 8am-6pm, but hours are flexible.
group id: 90736999
