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Job Requirements of Sr Quality Partner:
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Employment Type:
Contractor
-
Location:
Branchburg, NJ (Onsite)
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Sr Quality Partner
Careers Integrated Resources Inc
Branchburg, NJ (Onsite)
Contractor
Job Title: Senior Quality Partner
Location: Branchburg, NJ
Duration: 24-Month Contract
Shift: Standard Day Shift
Role Overview
As a Senior Quality Partner, you will serve as a strategic quality expert supporting operational excellence and compliance across departments. You’ll play a critical role in driving continuous improvement, enhancing quality systems, and fostering a culture of collaboration and accountability. This position is essential in ensuring the development and delivery of safe, high-quality products throughout the lifecycle.
Key Responsibilities
Drive Business Results & Ensure Compliance
Must Have:
Bachelor’s or Master’s degree in Life Science, Data Science, or related field.
Location: Branchburg, NJ
Duration: 24-Month Contract
Shift: Standard Day Shift
Role Overview
As a Senior Quality Partner, you will serve as a strategic quality expert supporting operational excellence and compliance across departments. You’ll play a critical role in driving continuous improvement, enhancing quality systems, and fostering a culture of collaboration and accountability. This position is essential in ensuring the development and delivery of safe, high-quality products throughout the lifecycle.
Key Responsibilities
Drive Business Results & Ensure Compliance
- Independently perform quality and regulatory activities to meet goals and objectives.
- Identify and implement process improvements in collaboration with management.
- Lead technical reviews and support documentation for audits and changes.
- Mentor and coach less experienced quality professionals.
- Communicate risks and issues that could impact product quality or compliance to executive leadership.
- Initiate and complete scheduled/unscheduled tasks with minimal supervision.
- Facilitate and implement cross-functional process improvements.
- Participate in and/or lead local and global projects or squads.
- Resolve complex issues that may affect broader organizational goals.
- Build strong partnerships across departments to ensure alignment and effectiveness.
- Promote a culture of continuous improvement and engrained quality at the site.
- Act as a role model for Agile leadership and Dia Operating Principles.
- Champion new, agile ways of working including collaborative decision-making and governance.
- Contribute to strategic goals, including expanding patient access and developing insight-driven diagnostic solutions.
Must Have:
Bachelor’s or Master’s degree in Life Science, Data Science, or related field.
- Equivalent technical/lab qualifications may be considered.
- 3–5 years in Quality Management, preferably with experience in multiple functions or global projects.
- Strong understanding of compliance, quality systems, and regulatory frameworks
- QA experience within pharmaceutical industry.
- Lead technical reviews and support documentation for audits and changes.
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