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Manufacturing Associate I/Ii

Aviva Systems Biology

This is a Contract position in Las Vegas, NV posted May 12, 2022.

Manufacturing Associate I/II Aviva Systems Biology is a fast-paced, mid-stage life sciences research tools company located in San Diego, CA.

We commercialize life science tools and reagents for research, drug discovery, and diagnostics.

Location: San Diego, CAHow will you make an impact?The Manufacturing Associate will assist in the production of recombinant proteins and other biological products under GMP guidelines.

Assist manufacturing team members to develop products in support of the company’s growth strategy.

This is a highly collaborative role where you will directly impact the company’s revenue growth.

The Manufacturing Associate works as part of a multidisciplinary team performing standard molecular biology techniques, protein purification and analysis, and cell culture maintenance.

Clear communication skills, careful execution with attention to details, and excellent record keeping are a must.

The ideal candidate will thrive in a fast-paced, dynamic environment as a part of a highly focused team of motivated scientists.

Job Responsibilities:Prepare buffers following GMP proceduresPerform preventative maintenance on manufacturing equipmentGrow microbes such as E.

coli and S.

cerevisiae for use in large-scale protein purificationMaintain, order, track, receive raw materials according to quality management systemWork with FPLC to purify proteins according to GMP guidelines for use in medical devicesEducation Requirements:B.S.

or M.S.

in life science or related subject.Experience Desired:1 year related laboratory experience in manufacturing is preferredBasic knowledge of standard laboratory equipment such as spectrophotometers, centrifuges, autoclaves, and biosafety cabinetFamiliarity with Microsoft Office Suite and/or other data analysis softwareSkills and AbilitiesCan demonstrate ability to follow protocols and GMP batch recordsShows good technique in laboratory operations such as pipetting, sterile culture, buffer preparation, and note keepingCan maintain clear communication between manufacturing supervisor, QC, and QA departments WORKING CONDITIONS Some heavy lifting, kneeling, squatting, etc.

may be required.You must be authorized to work in the United States without restriction or sponsorship.

Interested candidates should forward questions and a resume to