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Quality Specialist
Actalent
An engineering and sciences services and talent solutions firm connecting specialized experts with industry projects.
Responsible for managing and improving the Quality Management System in a Manufacturing Lab, ensuring compliance with analytical results and standard operating procedures.
19d ago
$35 - $4,327
Junior (1-3 years)
Contractor
Phillipsburg, NJ
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
corrective actions
document management
database management
data analysis
process validation
sop development
Implement corrective actions in processes as required.
Serve as document owner responsible for document creation, maintenance, and compliance for processes.
Manage and maintain databases for the quality system and prepare quality trending reports.
Perform standard quality assurance/quality control evaluation procedures, evaluate data using statistical methods for analysis, interpret results of analysis, and make recommendations to management.
Formulate and maintain Process Validation and QC objectives based on company vision and objectives.
Participate in quality and planning meetings and applicable Corrective Action Team activities.
Identify corrective actions in procedures and processes.
Plan, develop, and implement quality assurance programs.
Responsible for the continual improvement of the Quality Management System.
Create and develop or approve standard operating procedures.
Interact with associates, clients, and suppliers, maintaining an atmosphere of cooperation, teamwork, and respect even under stress.
Review and approve reports of analytical results/Certificate of Analysis for compliance evaluation.
Establish, coordinate, and monitor the Quality Management System.
Develop and present training for processes and procedures.
Work closely with managers and supervisors to plan, schedule, and implement QA related activities.
Prepare and maintain computer programs for compiling and statistical analysis of quality assurance data.
Investigate quality events, discrepancies, noncompliance issues, corrective and preventive actions reports, and complaints.
Complete audit paperwork as defined.
What you bring
biology
capa
bachelor's
data entry
reagents
gmp
Biology knowledge
Quality experience with CAPA and Investigations
Bachelor's Degree in Sciences
Data entry skills
Experience with reagents
Experience with GMP or GDP
Benefits
Time Off/Leave (PTO, Vacation or Sick Leave)
Health Spending Account (HSA)
Medical, dental & vision
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Critical Illness, Accident, and Hospital
Short and long-term disability
Transportation benefits
Employee Assistance Program
401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
Training + Development
Information not given or found
Interview process
Information not given or found
Visa Sponsorship
Information not given or found
Security clearance
completion of audit paperwork as defined.
eligibility for benefits may depend on job classification and length of employment.
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