Quality Control Senior Associate
Company: Actalent
Location: Thousand Oaks
Posted on: January 26, 2026
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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, Pomona , Quality Control Senior Associate, Engineering , Thousand Oaks, California
