Manufacturing Associate

**Manufacturing Associate**ManufacturingThousand Oaks, California, US+ Added - 04/06/2026_Our client, a renowned leader in biotechnology, is revolutionizing the use of living cells to create groundbreaking biologic medicines. As a guiding force in the biotech industry, they set the bar for innovation and advancement.__We are excited to announce a fantastic opportunity to join their team as a Manufacturing Associate!_**Location:** Ventura County, CA**Schedule** : M-F Days/Swing/Overnight (Looking for someone flexible as the shift will be changing!)**Pay rate** : $20/hr. - $25/hr. DOE**Job type:** 1 year contract (high chance of extension or conversion)**Responsibilities**+ Perform setup, cleaning, and sanitization of manufacturing equipment in accordance with SOPs and GMP guidelines+ Execute and monitor manufacturing operations under general supervision+ Follow all GMP documentation (SOPs, MPs) with strict adherence to safety, quality, and compliance requirements+ Conduct in-process sampling and support basic operation of analytical equipment+ Monitor critical processes and perform basic troubleshooting as needed+ Maintain accurate documentation, including equipment logs, batch records, and quality reports+ Assist in drafting, reviewing, and updating controlled documents such as SOPs and Manufacturing Procedures (MPs)+ Identify and support implementation of process improvements for routine operations+ Maintain a clean, organized, and compliant work environment at all times+ Work in a cleanroom environment while properly wearing required PPE (gowning, gloves, hairnet, steel-toe shoes, etc.)+ Collaborate effectively with team members to complete production goals safely and efficiently+ Perform physically demanding tasks including bending, lifting, climbing stairs/ladders (up to 6 feet), and extended periods of standing**Qualifications**+ High school diploma or GED and a minimum of 2 years of work or military experienceOR associate degree and a minimum of 6 months of work or military experience+ Ability to work in a regulated GMP environment following strict safety and quality standards+ Strong communication skills, both written and verbal+ Ability to work effectively in a team-oriented environment+ High attention to detail with strong focus on accuracy and compliance+ Ability to meet physical requirements of the role, including standing for long periods and performing repetitive tasks in a cleanroom setting+ Willingness to work varied shifts, including days, nights, weekends, holidays, and rotating schedulesINDBH\#LI-DNIWe are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.