QUALITY CONTROL ASSOCIATE - MCS

Position Quality Control Associate – MCS Location: Thousand Oaks, CA Category: Quality and Compliance Employment: Contract Worksite: On-Site Target Pay Range: 19-27/hr DOE Country: United States Job Summary This position is a unique opportunity to work within Quality Control at the Thousand Oaks site and to directly support both manufacturing and Quality Control operations. Under minimal supervision analyze environmental monitoring samples, cross‑check sample requirements against SOPs, and enter results in a laboratory information management system (LIMS) and/or SmartLab (LMES). This position will work in a team environment, collaborating within the lab as well as with various colleagues across the network. Key Responsibilities Align with safety guidelines from EHSS, cGMPs, and other applicable regulatory requirements at all times. Adhere to good documentation practices. Complete all required training before starting any tasks. Work efficiently and accurately with LIMS and/or SmartLab (LMES). Manage and coordinate assigned tasks, ensuring timely completion of all deliverables. Ensure equipment preventive maintenance is performed per requirements and due dates. Participate in investigations of out‑of‑specification and/or non‑conforming test results. Support internal and external inspections and audits (lab preparation, data retrieval, etc.). Troubleshoot, solve problems, and communicate with relevant team members. Implement prevention or corrective actions based on lab manager feedback. Perform QC support tasks such as organizing and cleaning the lab, ensuring removal of expired media, archiving documentation, and preliminary plate readings. Support the Microbiology lab with analytical testing. Implement lab improvements to ensure an efficient and productive lab environment. Willingness to work an on‑site Monday‑Friday (7 am‑4 pm) schedule and possibly weekend and holiday work based on business needs. Basic Qualifications Bachelor’s degree in a relevant scientific discipline or an appropriate specialty such as Life Sciences, plus one year of related experience or an equivalent combination of education and experience. Preferred Qualifications GxP experience, specifically practices and requirements in the testing of biopharmaceuticals. Experience using QC systems such as CDOCS (Veeva Vault), LIMS and/or SmartLab (LMES). Knowledge of Data Integrity Requirements in QC systems. Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint). Excellent problem‑solving capabilities and attention to detail for delivering right‑first‑time results. Experience collaborating within and across functional areas. Excellent written, verbal, and organizational communication skills, with attention to detail. Physical Requirements Frequently sit, grasp lightly, use fine hand manipulation, handle agar plates, perform desk‑based computer tasks, and lift, carry, push, and pull objects up to 15 pounds. Working Conditions Must perform tasks that require personal protective equipment such as safety glasses, shoes, lab coats, gloves, and possibly a mask. Equal Opportunity Employer We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. If you have a disability or require reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore appropriate arrangements. #J-18808-Ljbffr Planet Pharma