Manufacturing Associate I – Reagent and Cartridge Production at Alveo Technologies

Alameda, California, United States -

Full Time

Start Date

Immediate

Expiry Date

18 Aug, 26

Salary

27.07

Posted On

20 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Precision Assembly, GMP, GDP, Mechanical Aptitude, Automated Machinery Operation, QMS, PLM Software, ERP System, Kaizen, Cleanroom Protocols, Hand Tool Proficiency, Data Collection

Industry

Biotechnology Research

Description

About Alveo At Alveo Technologies, we are reshaping diagnostics for a healthier and more sustainable future. We are the first company to make molecular detection and diagnostics universally accessible – on the farm and in the field, clinic or manufacturing plant – helping to prevent or significantly limit the destructive impact of viruses, fungi, bacteria and other pathogens. By decentralizing molecular diagnostics across a broad range of industries, we are enabling rapid detection and decision making, timely action and better outcomes at the Point of Need™. Our portable, multiplex-capable diagnostic platform, Alveo Sense™, employs a patented method of direct electrical sensing of nucleic acid amplification to provide quick, affordable and accurate results. Through early pathogen detection, we help manage global animal and human health, food security, and supply chain resiliency by providing actionable insights at light speed. Know Sooner, Act Faster™ with Alveo. About the Role Alveo is looking for a skilled manufacturing professional who will be a valued member of our manufacturing operations. In this role, you will be part of a small and growing team of manufacturing staff, working to meet supply requirements while meeting our high-quality standards You’ll thrive here if you: Like being part of a team of production experts in a GMP manufacturing Clean Environment Room (CER). Check and maintain cleanliness and conditions within the CER; follow all CER protocols and cleaning procedures; and adhere to good GMP and GDP. Read, understand, and follow documented manufacturing instructions and workflows with attention to detail, precision, and care while collecting necessary product and quality data. Maintain workflow at a set cadence to ensure that daily output goals are achieved. Expertise with precision assembly, demonstrated attention to detail, and mechanical aptitude that includes use of small hand tools. Capable of operating semi-automated and automated machinery. Maintain and complete manufacturing records physically and/or electronically. Adhere to the existing programs and processes to deliver products that consistently meet specifications and quality requirements. Capable of executing regular maintenance checks and regular cleaning of machinery in addition to cleaning and preparing the CER before each shift. Participate in training and process improvement (kaizen) activities. Ensure consistent record-keeping in the Quality Management System (QMS), product lifecycle management (PLM) software, and enterprise resource planning(ERP) system. Adhere to best safety practices and documented procedures to ensure a safe working environment, including the use of PPE. What You Bring 2+ Years related experience; Previous experience working in a CER preferred. High school graduate or equivalent. Technical training or an associate's degree preferred. High attention to detail. Demonstrated ability to work collaboratively with other team members. Flexible in changing work activities. Physical Requirements: Good hand dexterity, able to perform precise tasks using tools such as tweezers or other hand tools. Able to work in CER. This is a non-exempt, hourly position. \n \n $23.08 - $27.07 an hour \n We are an equal opportunity employer and value diversity at Alveo Technologies. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Responsibilities

The role involves producing reagents and cartridges within a GMP Clean Environment Room while adhering to strict quality and safety protocols. Responsibilities include operating automated machinery, maintaining manufacturing records, and participating in process improvement activities.