What are the responsibilities and job description for the Manufacturing Associate III position at Alveo Technologies?
About Alveo
Alveo Technologies is the first company to make molecular detection and diagnostics universally accessible – on the farm, in the field, in the clinic, or in the manufacturing plant – helping prevent or significantly limit the destructive impact of viruses, fungi, bacteria, and other pathogens by detecting earlier at the Point of Need™. Alveo’s rugged and portable, multiplex-capable diagnostic platform employs IntelliSense™, its patented method of direct electrical sensing of nucleic acid amplification to provide affordable, rapid, and accurate results. By enabling early pathogen detection, Alveo helps manage global health, food security, and supply chain resiliency by providing actionable insights at lightspeed. Know Sooner, Act Faster™ with Alveo. For more, visit: https://www.alveotechnologies.com/
Alveo is looking for a skilled manufacturing professional to join our internal Reagent Manufacturing operations. In this role, you will be part of a small and growing team of reagent manufacturing colleagues working together to meet reagent supply requirements and our high-quality standards.
You Will:
Be part of a team of production experts in a GMP/GLP formulations/compounding lab as well as cartridge manufacturing.
Manufacture reagents, buffers and cartridge assemblies in compliance with cGMP, cGLP, GDP, QSRs, ISO and IVD regulations.
Follow production management controls, tools, and reporting.
Adhere to the existing programs and processes to deliver reagents that consistently meet specifications and quality requirements batch-after-batch.
Follow detailed work instructions and collect necessary product and quality data.
Assist in process improvements/implementations that works towards team goals.
Pay attention to details to perform consistent and quality work without excessive supervision.
Assist leadership with troubleshooting and handling of process deviations.
Assist with root cause and corrective actions.
Ensure consistent record-keeping in the Quality Management System (QMS), product lifecycle management (PLM) software, and enterprise resource planning(ERP) system.
Understand and assist with requests for raw materials needed for production.
Adhere to best safety practices and documented procedures to ensure a safe working environment, including use of PPE.
Your Background Should Include:
Bachelor or Associate Degree (BA, BS, AS, AAS) with a focus on chemical and/or biological sciences required.
3 Years related experience in a GMP/GLP formulations/compounding lab required.
Must be able to work in a fast-paced environment, managing multiple competing priorities and assignments with the ability to plan and deliver against deadlines.
Strong computer and scientific skills with attention to detail.
Strong organizational skills to maintain a timely production turn around time.
Strong written and verbal communication skills required.
Laboratory experience including pipetting, safety, and hazardous materials handling, and working in a BSC is strongly preferred.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Familiarity with cell and nucleic acid amplification assays.
Strong understanding of basic laboratory equipment.
Experience with process scale up is strongly preferred.
This is a non-exempt position. Salary range is $25.79 - $30.41 per hour.
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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.
Salary : $26 - $30
