QA Product Manager (Sterile Products) - Contractor

Joulé

Florham Park, NJ

JOB DETAILS
SALARY
$65–$85 Per Hour
SKILLS
Change Control, Computer Skills, Contract Manufacturing, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Drug Manufacturing, Drug Products, FDA (Food and Drug Administration), ICH Regulations, Maintain Compliance, Manufacturing, Microsoft Excel, Microsoft Outlook, Microsoft Word, Negotiation Skills, Outsourcing, Problem Solving Skills, Product Management, Product Support, QA Partner Testing Software, Quality Assurance, Quality Management, Quality Monitoring, Regulations, Regulatory Requirements, Service Delivery, Supply Chain, Support Documentation, Time Management
LOCATION
Florham Park, NJ
POSTED
Today

Job Title: QA Product Manager (Sterile Products) - Contractor

Location: Florham Park, New Jersey

Type: Contract

Compensation: $65.00 - $75.00 per hour dependent on years of experience and education.

Contractor Work Model: Hybrid – onsite and remote

Hours: 40.0 hours per week

Overview

Responsibilities

  • Review manufacturing and packaging batch records; escalate issues and perform final disposition of assigned products.
  • Support and coordinate investigations (deviations, OOS/OOT, product complaints), initiate CAPAs, and ensure timely closure.
  • Maintain ongoing communication with contract manufacturers to resolve quality issues, monitor compliance, and ensure product release readiness.
  • Provide QA input during regulatory inspections and support documentation needs (change controls, stability protocols, technical agreements).
  • Assist in ensuring that audit findings are tracked and CAPAs are effectively implemented.
  • Collaborate with Supply Chain, Regulatory, and other partners to ensure continued product quality and supply continuity.
  • Lead large-scale technology transfers.
  • Build or negotiate new or existing quality agreements.
  • Provide support for Developmental Products as needed.

Requirements

  • Minimum 4 years of experience of QA experience in sterile drug product manufacturing/oversight.
  • Strong background in batch record review, CAPA management, and sterility assurance.
  • Direct experience with third-party (CMO) oversight.
  • Able to operate independently with minimal supervision.
  • Comfortable working cross-functionally and representing QA in external partner interactions.
  • Experience with quality management software and tools such as Veeva including demonstrated computer experience with MS Word, Excel, and Outlook.
  • Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

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Ref: #568-Clinical


About the Company

J

Joulé

With extensive scientific, clinical, and healthcare industry experience, Joulé recruiters excel at placing talent across core specialty areas:

  • Scientific staffing for hard-to-find skills

Working across every scientific discipline, Joulé places biologists, chemists, scientists, technicians and other specialists.

  • Clinical lifecycle recruiting

From research to regulations, safety to statistics, Joulé helps clients manage every stage of the clinical development lifecycle.

  • Equipment calibration, maintenance and validation

Laboratory and facility support comes with a total quality commitment backed by ISO 9001:2008 certification.

  • National healthcare recruitment

Trust Joulé’s extensive experience in physician, advanced practice provider and executive direct placement search.

COMPANY SIZE
500 to 999 employees
INDUSTRY
Biotechnology/Pharmaceuticals
WEBSITE
https://www.jouleinc.com/