Quality Control Senior Associate

Company: Actalent
Location: Thousand Oaks
Posted on: January 26, 2026

Job Description:

Job Description Job Description Job Title: Quality Control Senior Associate Job Description We are seeking a diligent and detail-oriented Quality Control Senior Associate to join our team. This position offers the flexibility to work remotely or in a hybrid capacity, with a work schedule during the dayshift. The role focuses on executing deliverables for a project to implement a new fully Electronic Lab Notebook (ELN) system, and it is not a laboratory testing position. Responsibilities include the design, configuration, and validation of the new ELN system, recreation and/or migration of required master data, and involvement in the deployment of production instances at the sites. The successful candidate will work under BPO supervision, adhering to established procedures, Standard Operating Procedures, and Work Instructions for safety and cGMP/CFR requirements. Collaboration with colleagues across the network to ensure project commitments are met is key, along with reporting status updates and escalating issues through the project management team. Responsibilities Participate in process engineering activities. Facilitate the development of new business SOPs, forms, and manuals using new processes and workflows. Participate in system requirement, software configuration, and design activities. Receive and/or verify master data for the sites. Coordinate ELN Template development and review with site SMEs. Support the development and review of Operational Qualifications. Execute User Acceptance Testing and Data Migration Verification. Review and provide input on training materials. Support training material development by providing inputs and reviews. Support site Instrument Qualification activities, including planning and execution. Essential Skills Experience with Electronic Lab Notebooks (ELN). Knowledge in Quality Management Systems (QMS) and quality assurance. Experience in the medical device or pharmaceutical industries. Understanding of GDP and GLP practices. Additional Skills & Qualifications Bachelor's degree and 2 years of industry Quality Control or Quality experience, OR Associate's degree and 6 years of industry Quality Control or Quality experience, OR High school diploma/GED and 8 years of industry Quality Control or Quality experience. Work Environment The position offers the flexibility of working in a remote or hybrid setup, requiring attendance in the office three days a week. The role operates during the dayshift and involves collaborating with a team in a supportive environment. The work environment emphasizes adherence to established procedures, safety standards, and documentation practices. Job Type & Location This is a Contract position based out of Thousand Oaks, CA. Pay and Benefits The pay range for this position is $37.00 - $43.00/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 hybrid position in Thousand Oaks,CA. Application Deadline This position is anticipated to close on Feb 5, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Keywords: Actalent, Covina , Quality Control Senior Associate, Engineering , Thousand Oaks, California