Job Information
Actalent MCS Quality Control Associate in Thousand Oaks, California
Job Title: MCS Quality Control AssociateJob Description
The MCS Quality Control Associate performs routine laboratory procedures and analytical testing in a regulated quality control environment to support ongoing laboratory operations. Working under general supervision, this role focuses on executing cell-based potency assays and ligand-binding assays, accurately documenting and interpreting data, and maintaining compliance with cGMP, CFR, and internal quality standards. The position is ideal for a life sciences graduate with hands-on laboratory and GMP experience who thrives in a collaborative, fast-paced setting and demonstrates long-term commitment to their roles.
Responsibilities
Perform routine laboratory procedures in a regulated quality control environment, including sample preparation and execution of analytical tests.
Conduct routine analytical testing, including cell-based potency assays and ligand-binding assays such as ELISA, following established protocols and regulatory guidelines.
Use core laboratory techniques such as accurate pipetting, preparation of serial dilutions, and operation of automated liquid handling systems.
Document, compute, compile, interpret, and enter data in laboratory notebooks and electronic systems with a high level of accuracy and attention to detail.
Maintain, operate, and troubleshoot specialized laboratory equipment to ensure reliability and readiness for testing.
Initiate and implement changes to controlled documents in accordance with internal procedures and regulatory expectations.
Learn, understand, and comply with all applicable safety guidelines, cGMPs, and CFRs, including maintenance of training records, laboratory documentation, written procedures, building monitoring systems, and laboratory logbooks.
Evaluate documentation and data according to internal quality standards and regulatory requirements, identifying any discrepancies or issues.
Organize daily work efficiently, handle multiple priorities, and meet required deadlines for testing and documentation.
Communicate effectively with team members, providing clear written and oral updates on work status, issues, and results.
Demonstrate strong conflict resolution skills and contribute positively to collaboration within a small team environment.
Recognize when and how to appropriately escalate issues that may impact data integrity, compliance, safety, or timelines.
Identify, recommend, and potentially implement improvements related to routine job functions, workflows, or documentation practices.
Maintain a high level of flexibility and adaptability in response to changing priorities, project needs, and regulatory requirements.
Essential Skills
Bachelor’s degree in a Life Science discipline such as Biology, Chemistry, Biochemistry, or a related field.
Hands-on laboratory experience in a regulated environment, preferably within pharmaceutical, biotechnology, or academic settings.
GMP or cGMP experience in a quality control or similarly regulated laboratory environment.
Practical experience performing analytical testing, including cell-based potency assays and ligand-binding assays (for example, ELISA).
Demonstrated proficiency in core laboratory techniques, including accurate pipetting and preparation of serial dilutions.
Experience using automated liquid handling systems in a regulated QC environment.
Basic proficiency with Microsoft Excel and Word for data entry, documentation, and reporting.
Ability to adhere strictly to regulatory requirements, written procedures, and safety guidelines.
Ability to evaluate documentation and data according to internal and regulatory guidelines.
Strong written and oral communication skills for clear documentation and effective teamwork.
Strong attention to detail and a high level of accuracy in all laboratory and documentation tasks.
Ability to organize work, manage multiple tasks simultaneously, and meet deadlines.
Flexibility and adaptability to changing priorities and requirements.
Understanding of regulatory requirements, safety guidelines, and factors that impact compliance.
Ability to recognize and appropriately escalate issues when necessary.
Demonstrated role longevity and commitment, with a consistent work history that reflects long-term engagement in prior positions.
Additional Skills & Qualifications
Experience working in a quality control laboratory environment supporting pharmaceutical, biotechnology, or academic research activities.
Familiarity with maintaining training records, laboratory documentation, written procedures, building monitoring systems, and laboratory logbooks in compliance with cGMP and CFR requirements.
Experience identifying, recommending, and implementing process improvements within routine laboratory functions.
Strong interpersonal skills, including the ability to resolve conflicts constructively within a small team.
Self-starting initiative with the ability to work independently under general supervision while contributing to team goals.
Work Environment
This is a full-time, on-site laboratory role with a standard schedule of Monday through Friday from 8:00 AM to 5:00 PM, with occasional overtime approximately once a month on a weekend day as operational needs arise. The work takes place in a regulated quality control laboratory that operates under cGMP and CFR guidelines, with a strong emphasis on safety, documentation integrity, and compliance. The environment involves regular use of specialized laboratory equipment, automated liquid handling systems, and standard computer applications such as Excel and Word for data entry and reporting. Team members work closely in a small, collaborative group that values clear communication, reliability, and mutual support. Appropriate laboratory attire and adherence to all safety and procedural requirements are expected at all times.
Job Type & Location
This is a Contract position based out of Thousand Oaks, CA.
Pay and Benefits
The pay range for this position is $25.00 - $25.00/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 Thousand Oaks,CA.
Application Deadline
This position is anticipated to close on May 5, 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.