Quality Control Analyst

Quality Control Analyst, Sample Management As a Quality Control Analyst in Sample Management, you will play a critical role in maintaining the lifecycle of quality control samples. This includes ensuring accurate receipt, labeling, aliquoting, storage, distribution, and disposal of samples in compliance with regulatory and company standards. You will support laboratory operations by maintaining sample inventory systems, preparing samples for testing, and ensuring proper documentation and traceability. Collaboration with QC laboratories, manufacturing, and logistics teams is essential to ensure timely sample availability while adhering to Good Manufacturing Practices (GMP) and data integrity requirements. Responsibilities + Receive, log, and label incoming samples in accordance with SOPs and regulatory requirements. + Maintain accurate sample tracking using paper-based logs and electronic systems such as LIMS. + Ensure proper storage of samples, including temperature-controlled environments and stability chambers. + Coordinate sample distribution to QC laboratories for testing. + Monitor critical reagent and reference standard inventory levels. + Manage the sample lifecycle from receipt through disposal. + Prepare and aliquot samples for testing while maintaining the chain of custody. + Ensure compliance with GMP, GDP, and data integrity standards. + Review and verify sample-related documentation and equipment logbooks for accuracy and completeness. + Support stability studies by managing sample pulls and tracking time points. + Coordinate with manufacturing and logistics teams for sample requests and timelines. + Perform biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines. + Assist with SOP creation, revision, and training related to sample management processes. + Identify and contribute to deviation and laboratory investigations, including sample discrepancies and OOS/OOE/OOT events. + Maintain the laboratory in an inspection-ready state. + Hold self and others accountable to abide by department and company policies and practices. + Adhere to cGMP, 21CFR, USP, EP, ICH, and other applicable regulatory requirements. + Perform sampling and testing of incoming raw materials. Essential Skills + Experience maintaining cGMP compliant Quality Control and Stability laboratories. + Ability to follow written instructions and perform tasks with direct or minimal supervision. + Capability to work independently as well as in a team environment. + Familiarity with Laboratory Information Management Systems (LIMS). + Proficient in using computers, including Windows, Microsoft Word, and Excel. + Strong written and verbal communication skills. + Strong documentation skills are essential. Additional Skills & Qualifications + B.S./B.A./A.A. in Science or a related field such as biology, biochemistry, or chemistry. + Minimum of 2 years of relevant laboratory experience in a GMP environment is desired. Work Environment The position requires the ability to occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, depth perception, and the ability to adjust focus. The work environment involves maintaining GMP operations in a Quality Control laboratory, ensuring adherence to Good Documentation Practices, proper sample handling, and chain of custody. The role requires compliance with Standard Operating Procedures and an understanding of regulatory requirements, with proficiency in using LIMS and supporting inspections and quality audits. Job Type & Location This is a Contract to Hire position based out of Vacaville, CA. Pay and Benefits The pay range for this position is $30.00 - $35.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: u2022 Medical, dental & vision u2022 Critical Illness, Accident, and Hospital u2022 401(k) Retirement Plan u2013 Pre-tax and Roth post-tax contributions available u2022 Life Insurance (Voluntary Life & AD&D for the employee and dependents) u2022 Short and long-term disability u2022 Health Spending Account (HSA) u2022 Transportation benefits u2022 Employee Assistance Program u2022 Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Vacaville,CA. Application Deadline This position is anticipated to close on Apr 13, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people Actalent is an equal opportunity employer. About Actalent Actalent is a global leader in engineering and sciences services. For more than 40 years, weu2019ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APACu2014with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at .

Created: 2026-04-09