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Quality Manager, Logistics

Parexel -
Quakertown, PA

Apply Now

Job Details

$110,000 a year
1 day ago

Benefits

Health savings account
Health insurance
Dental insurance
Tuition reimbursement
Paid time off
Vision insurance
401(k) matching
Life insurance
Pet insurance

Qualifications

Health Care Logistics
Biological safety protocols
Regulatory inspections
Drug regulation
Compliance audits & assessments
Good documentation practices (GDP)
English
GMP
Quality control audit
ICH guidelines
Quality assurance experience within pharmaceutical industry
Quality inspection
Regulatory readiness in healthcare
Clinical research inspection readiness
Quality control experience within pharmaceutical industry
Research regulatory compliance
Quality audits
Logistics compliance
State and federal pharmacy laws
Healthcare compliance
Audit support
Quality assurance experience within healthcare

Full Job Description

About Parexel

Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose - moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart®.

About the Role

We are seeking a Quality Manager, Logistics to join our team onsite out of our Quakertown, PA location. As a Quality Manager, Logistics, you will drive quality excellence and operational compliance across our clinical supply chain and logistics operations. This position plays a key role in ensuring regulatory adherence, maintaining Good Manufacturing Practices GMP/ Good Clinical Practices GDP standards, and supporting the safe and timely delivery of clinical trial supplies to research sites worldwide. You'll collaborate with cross-functional teams, champion process improvements, and contribute to supply chain operations from planning through closeout.

You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through quality assurance, process optimization, and regulatory compliance. With diverse teams and continuous learning opportunities, the Quality Manager, Logistics can explore career paths and expand skills across clinical research operations and quality management.

Key Responsibilities

Identify process improvement opportunities and champion their implementation across logistics and quality operations
Provide expert quality consultancy to operational groups, functional leads, and project teams while maintaining independence and objectivity
Mentor, train, and provide leadership direction to Quality Specialists and depot staff, fostering a culture of continuous improvement and compliance
Oversee quality management projects including validation review and approval processes, change request management, and quality investigations
Verify compliance with GxP guidelines, ICH-GCP standards, FDA, DEA, and local regulations across all designated operational areas
Support identification, management, and prevention of quality issues through facilitation of corrective and preventive action (CAPA) programs
Provide audit and inspection support, including preparation assistance, representation during regulatory audits, and response review
Execute QC release of medicinal products and clinical trial supplies; oversee QC activities and premise/equipment maintenance in depot and warehouse environments
Manage US state registrations, depot distribution licensing activities, and qualified officer responsibilities for Biosafety level; BSL-1 and BSL-2 operations
Assist with collection and reporting of quality metrics; remain informed about regulatory developments and share insights with the quality and operations teams
Receive approval from local QPs (Qualified Person), RPs (Responsible Pharmacist) or APs (Authorized Persons) before entering into the HQC-role

Candidate Profile

You'll thrive in this role if you bring:

Strengths in quality management, regulatory compliance, and process improvement, including oversight of quality management systems.
Experience performing QP Audits, on-site audits, conducted to evaluate whether a site complies with GMP standards.
Experience working in clinical research, healthcare, logistics, or a regulated environment
The ability to collaborate across teams, mentor staff, and communicate clearly with diverse stakeholders
A patient-focused mindset and strong attention to detail in high-stakes operations
Comfort working with quality management systems, Microsoft Office applications, and general IT literacy
You have experience managing facility licenses, including state medical drug distribution

Required Qualifications

Bachelor's degree in technology, biological science, pharmacy, or other health-related discipline, or equivalent qualification or clinical research experience
Relevant experience in Quality Management, clinical research operations, or Logistics Quality Management (LQM) support
Knowledge of GMP/GDP regulations (Good Distribution Practices), ICH-GCP standards, and clinical trial processes
Experience with distribution licensing, QP, GMP and GxP auditing, and quality management systems
Experience with BSL level 1 and 2 operations and distribution of medical supplies, drugs, or devices

Strong communication, organization, and problem-solving skills with the ability to work independently and take initiative
English proficiency (written and oral English)

Preferred Qualifications

Bachelors or Master's degree in a science, technology, or industry-related discipline
Trainer's experience and expertise in developing training materials and mentoring programs
Experience performing QP Audits
Experience managing distribution state licenses and licensing requirements
Oversight of quality management systems
Ability to travel approximately 20-30%
Experience with radiopharmaceutical operations and oversight
Familiarity with FDA, DEA, and state regulatory requirements for depot operations
Experience managing multiple complex projects simultaneously across different operational areas

Benefits and Compensation

Health, Vision & Dental Insurance
Tuition Reimbursement
Vacation/Holiday/Sick Time
Flexible Spending & Health Savings Accounts
Work/Life Balance
401(k) with Company match
Pet Insurance
For a complete list of benefits, please visit www.parexel.com/us-benefits

The potential base pay range for this role is $110,000. The actual salary offered may vary within this range based on several factors, including the position and level offered, skills, education, training, experience, professional achievements, and location.

Some roles may also be eligible for additional incentives, bonuses, or other compensation programs. Our Talent Acquisition team will provide details on applicable bonus plans or incentive structures for eligible positions.

We offer a comprehensive benefits package to eligible employees, which includes paid time off, a 401(k) match, life insurance, health insurance, and additional benefit offerings in accordance with the terms of our applicable plans.

If this job doesn't sound like the next step in your career, but perhaps you know of someone who'd be a perfect fit, send them the link to apply!

We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.

Apply Now

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