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QC Associate
Actalent
An engineering and sciences services and talent solutions firm connecting specialized experts with industry projects.
Perform QC release assays, sterility checks, and support quality control for manufacturing.
2d ago
$26 - $28
Junior (1-3 years)
Contractor
Emeryville, CA
Onsite
Company Size
5,000 Employees
Service Specialisms
Technical consultation
Performance analysis
Physical development
Injury prevention and recuperation
Sports psychology
360° Marketing
Consultancy with clubs and sporting entities
Legal services
Sector Specialisms
Utilities
Power
Automotive
Food and Beverage
Consumer Products
Industrial Goods
Manufacturing
Mechanical Engineering
Role
What you would be doing
product validation
qc testing
equipment qualification
documentation management
sterility checks
lot release
Conduct validation of products using in-house assays.
Conduct or assist with deviation initiation, lab investigation, change controls, document change orders, and CAPA execution related to QC testing.
Assist with equipment qualification/validation protocols, reports, and other documentation.
Organize and maintain logs and all related documentation according to the SOPs.
Maintain standards for reliability and performance of production.
Conduct routine QC release assays such as cell count, viability, and purity.
Conduct routine sterility checks and prepare samples for viral testing.
Execute quality improvement testing and activities.
Conduct Batch Record reviews and Material Disposition for Fresh Send-Outs.
Work with both the Manufacturing and Quality teams to ensure optimum lot release workflow and improve existing products.
What you bring
bsc
biotech
cellular biology
glp
problem solving
teamwork
Flexibility to wear multiple hats within the organization.
Good conceptual, analytical, problem-solving, planning, and organization skills.
Excellent oral and written interpersonal communication skills.
Critical thinker with the ability to read, analyze, and interpret technical data.
Experience with laboratory procedures and techniques.
Working knowledge of quality systems and Good Laboratory Practices (GLP).
Ability to prioritize and adapt to changing priorities while maintaining a high-quality standard.
Ability to multi-task and assist other departments as needed.
Bachelor of Science degree or equivalent in molecular biology, chemistry, or life science-related field.
Ability to motivate and work effectively within a team.
Minimum of 1-2 years in a Biotechnology role. Experience in cellular biology is preferred.
Benefits
Time Off/Leave (PTO, Vacation or Sick Leave)
Health Spending Account (HSA)
Employee Assistance Program
401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
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