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Quality Specialist
- Actalent (Phillipsburg, NJ)
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Job Title: Quality SpecialistJob Description
As a Quality Specialist, you will be responsible for the continual improvement and management of the Quality Management System. You will work closely with managers and supervisors to plan, schedule, and implement quality assurance activities, ensuring compliance with analytical results and standard operating procedures.
Responsibilities
+ Responsible for the continual improvement of the Quality Management System.
+ Establish, coordinate, and monitor the Quality Management System.
+ Work closely with managers and supervisors to plan, schedule, and implement QA related activities.
+ Plan, develop, and implement quality assurance programs.
+ Implement corrective actions in processes as required.
+ Review and approve reports of analytical results/Certificate of Analysis for compliance evaluation.
+ Create and develop or approve standard operating procedures.
+ Serve as document owner responsible for document creation, maintenance, and compliance for processes.
+ Prepare and maintain computer programs for compiling and statistical analysis of quality assurance data.
+ Develop and present training for processes and procedures.
+ Investigate quality events, discrepancies, noncompliance issues, corrective and preventive actions reports, and complaints.
+ Identify corrective actions in procedures and processes.
+ Manage and maintain databases for the quality system and prepare quality trending reports.
+ Participate in quality and planning meetings and applicable Corrective Action Team activities.
+ 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.
+ Interact with associates, clients, and suppliers, maintaining an atmosphere of cooperation, teamwork, and respect even under stress.
+ Complete audit paperwork as defined.
Essential Skills
+ Bachelor's Degree in Sciences
+ Quality experience with CAPA and Investigations
+ Experience with GMP or GDP
Additional Skills & Qualifications
+ Biology knowledge
+ Data entry skills
+ Experience with reagents
Work Environment
This position is based in a Manufacturing Lab located in Phillipsburg, NJ, USA. The work environment fosters collaboration and teamwork, ensuring a cooperative atmosphere even in stressful situations.
Job Type & Location
This is a Contract to Hire position based out of Bridgewater, New Jersey.
Pay and Benefits
The pay range for this position is $35.00 - $43.27/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 Phillipsburg,NJ.
Application Deadline
This position is anticipated to close on Oct 10, 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 [email protected] (%[email protected]) for other accommodation options.
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