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MCS Associate Quality Control

Actalent
CONTRACTOR Remote · US Thousand Oaks, CA, Ventura, US USD 56160–58240 / month Posted: 2026-05-11 Until: 2026-07-10
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Job Description
Actalent is Hiring for a Quality Control Associate in the Thousand Oaks area! Job Description The MCS Associate Quality Control position offers a unique opportunity to work within the Quality Control organization at a biopharmaceutical manufacturing site, directly supporting both manufacturing and Quality Control operations. The role focuses on microbiology and environmental monitoring, including analytical testing, data entry into laboratory information systems, and adherence to cGMP and data integrity requirements. The successful candidate will work in a collaborative lab environment, supporting routine operations, investigations, audits, and continuous improvement activities. Responsibilities Analyze environmental monitoring samples under minimal supervision and ensure all sample requirements comply with applicable standard operating procedures. Enter test results accurately and efficiently into Laboratory Information Management Systems (LIMS) and/or SmartLab LMES. Consistently follow safety guidelines from Environmental Health, Safety and Sustainability (EHSS), current Good Manufacturing Practices (cGMP), and other applicable regulatory requirements. Adhere to good documentation practices, ensuring records are complete, accurate, and compliant with data integrity standards. Complete all required training before performing any assigned tasks or laboratory activities. Manage and coordinate assigned tasks, prioritizing workload to complete all deliverables in a timely manner. Ensure preventive maintenance and calibrations for laboratory equipment are performed as required and completed by their due dates. Participate in the investigation of out-of-specification and/or non-conforming test results, providing data, observations, and technical input as needed. Support internal and external inspections and audits, including laboratory preparation, data retrieval, and documentation support. Troubleshoot and resolve routine laboratory issues, communicating findings and progress to relevant team members. Implement preventive or corrective actions in the laboratory based on feedback from lab leadership and quality systems. Perform Quality Control support tasks such as organizing and cleaning the laboratory, checking and removing expired media, archiving documentation, and performing preliminary plate readings. Support the Microbiology laboratory with analytical testing, including pipetting, water testing, and observing colonies on agar plates. Work in a laminar flow hood while maintaining aseptic technique and compliance with microbiological best practices. Contribute to the implementation of laboratory improvements to enhance efficiency, productivity, and compliance. Collaborate effectively within the laboratory team and with colleagues across the broader network to achieve shared goals. Work an on-site schedule Monday through Friday (typically 8:00 AM – 5:00 PM or 7:00 AM – 4:00 PM), with flexibility to support possible weekend and holiday work based on business needs. Maintain a high level of attention to detail to deliver right-first-time results in all testing and documentation activities. Essential Skills Bachelor’s degree in a relevant scientific discipline or appropriate specialty such as Life Sciences, plus one year of related experience, or an equivalent combination of education and relevant work experience. Background in biology or microbiology with hands-on laboratory and benchwork experience. Experience with microbiology techniques, including pipetting, water testing, and observing colonies on agar plates. Exposure to cGMP or GxP environments and understanding of aseptic technique. Ability to work with Laboratory Information Management Systems (LIMS) and/or SmartLab LMES with efficiency and accuracy. Strong attention to detail and commitment to delivering accurate, right-first-time results. Ability to manage multiple tasks, prioritize work, and meet deadlines in a fast-paced environment. Effective written and verbal communication skills for documentation, collaboration, and interaction with cross-functional teams. Capability to troubleshoot routine laboratory issues and contribute to problem-solving efforts. Physical ability to frequently sit, grasp lightly, perform fine hand manipulation, handle agar plates repetitively, perform desk-based computer tasks, and lift, carry, push, or pull objects up to 15 pounds. Willingness and ability to work on-site full-time with flexibility for potential weekend and holiday shifts based on business requirements. Additional Skills & Qualifications GxP experience, particu