Quality Control Specialist (2nd Shift)

Job Description

This role involves conducting incoming, in-process, and final release quality control testing within a controlled manufacturing environment. Responsibilities extend to executing validation studies, analyzing data, generating analytical reports, investigating non-conformances, evaluating processes and procedures, utilizing statistical techniques, and inspecting and testing equipment. The position may also require conducting training on quality-related tools, methods, and procedures, and interacting with R&D, Manufacturing, Quality, and Supply Chain teams, as well as customers and suppliers on quality-related issues.

Responsibilities

• Conduct incoming, in-process, and final release QC testing.
• Execute validation studies and test protocols.
• Analyze data and generate analytical reports.
• Investigate non-conformances and evaluate processes and procedures.
• Utilize statistical techniques and review specifications.
• Inspect and test equipment.
• Conduct training on quality-related tools, methods, and procedures.
• Interface with R&D, Manufacturing, Quality, and Supply Chain teams.
• Participate in departmental projects and investigations as needed.
• Monitor inventory levels daily.
• Complete batch records while maintaining good documentation practices.
• Prepare/formulate QC test solutions following standard operating procedures.

• B.S. degree in basic sciences, life sciences, or engineering.
• Three years of relevant experience in a QC capacity preferred.
• Familiarity with cGMP and ISO standards.
• Proficiency in molecular techniques such as DNA extraction and PCR amplification.
• Knowledge of safety precautions for biohazards and bloodborne pathogens.
• Understanding of the Quality System and ability to execute change orders.
• Basic statistical knowledge for interpreting scientific data.

• Technical knowledge of molecular biology, including principles of nucleic acid hybridization, probe and primer design, and enzymatic amplification of specific gene sequences.
• Ability to assist with special projects and perform additional duties as required.

The role operates within a GMP, ISO certified or FDA workplace, adhering to safety standards and requirements. The work environment involves handling biohazards and requires knowledge of related safety precautions. This is a 2nd shift position, Monday- Friday 11:30am-8:00pm

The pay range for this position is $27.22 - $27.22/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 Carlsbad,CA.

Application Deadline

This position is anticipated to close on Jul 9, 2025.

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 ... for other accommodation options.