Quality Control Analyst

QC Analyst- Pharmaceutical Job Description Join a dynamic team as a Quality Control Analyst where you will perform essential biochemical, physical, and chemical evaluations of process development, lot release, and stability samples in compliance with cGMP guidelines. This role requires a commitment to safety and quality, with opportunities for training on advanced analytical methods. Responsibilities Perform biochemical, physical, and chemical analyses of test samples under cGMP with direct or minimal supervision to meet specified timelines. Provide technical support for troubleshooting test methods as needed. Identify and contribute to Out of Specification (OOS), Out of Expectation (OOE), and Out of Trend (OOT) investigations related to testing performed. Initiate and author deviation and laboratory investigations. Maintain the laboratory in an inspection-ready state. Develop and maintain proficiency in a broad range of trained test methods. Train analysts on test methods and procedures. Author Change Control records and lead the revision of written procedures as assigned. Ensure compliance with cGMP, 21CFR, USP, EP, ICH, and other applicable regulatory requirements. Manage reagent and equipment inventory for assigned areas of responsibility. Responsible for sampling and testing of incoming raw materials. Essential Skills Strong working knowledge of cGMP regulations, including 21CFR 210 & 211, USP, EP, and ICH. Ability to follow written instructions and perform tasks with direct or minimal supervision. Capable of working independently as well as in a team environment. Proficient in Windows, Microsoft Word, and Excel. Strong written and verbal communication skills. Excellent documentation skills. Ability to develop skills in the operation and maintenance of various analytical instruments. Additional Skills & Qualifications Experience with Protein analytics, SDS-PAGE, separations technology for HPLC, Chromatography Data Systems (CDS) software such as OpenLab, subvisible particles testing (USP ), and Container Closure Integrity Testing (CCIT) is preferred.

B.S./B.A.

in Science or related field with a major in biology, biochemistry, or chemistry. Minimum of 5 years of relevant laboratory experience in a GMP environment is desired. Ability to occasionally lift and/or move up to 25 pounds. Specific vision abilities required include close vision, depth perception, and ability to adjust focus. Work Environment The work environment promotes a friendly culture with an emphasis on collaboration and adherence to safety protocols. The facility operates with advanced technologies and requires a commitment to quality standards in a professional laboratory setting. 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 $35.00 - $40.00/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:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• 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 17, 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, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with 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 actalentservices.com.