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Quality Specialist I Logistics

Parexel -
Quakertown, PA

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Job Details

$24 - $33 an hour

Benefits

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

Qualifications

Pharmaceutical regulatory compliance
ICH guidelines
Clinical research compliance
Quality assurance experience within pharmaceutical industry
Quality control experience within pharmaceutical industry
Clinical quality assurance standards

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 Specialist I to join our team in an on-site capacity at our North America Distribution Center in Quakertown, PA. As a Quality Specialist I, you will support quality operations that help bring life-changing medicines to patients. This position plays a key role in quality assurance, regulatory compliance, and clinical supply chain integrity. You'll collaborate with cross-functional teams, follow industry-standard processes, and contribute to quality operations from receipt through distribution. Responsibilities include executing quality checks on medicinal products, performing quality control tasks in depot and warehouse operations, and providing quality consultancy to operations personnel.

You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through quality assurance, process improvement, and regulatory excellence. With diverse teams and continuous learning opportunities, the Quality Specialist I can explore career paths and expand skills across clinical research and supply chain operations.

Key Responsibilities

Execute quality checks of medicinal products and clinical trial supplies during receipt, production, and distribution
Perform quality control tasks in depot and warehouse operations as assigned
Undertake local quality management tasks as described in Parexel controlled documents
Provide support for change control management related to premises, equipment, and processes
Support premise and equipment maintenance and cleaning activities
Perform reviews of Production Batch Records and support qualification and validation activities
Participate in Standard Operating Procedure (SOP) and process development initiatives
Serve as a quality consultant to operational groups, including process authoring, review, and expertise in GxP guidelines
Contribute to the development of training materials as a process subject matter expert
Support identification, management, and prevention of quality issues through audit and inspection support
Provide quality consultancy to operations personnel and verify compliance with GxP guidelines and regulations

Candidate Profile

You'll thrive in this role if you bring:

Excellent interpersonal, verbal, and written communication skills
Ability to take initiative with a flexible approach to work assignments and new learning
Critical thinking with a patient and client-focused mindset
Strong organizational skills with the ability to manage multiple and varied tasks with attention to detail
Capability to work independently and collaboratively as part of a team
Attention to quality and compliance in a regulated environment

Required Qualifications

Bachelor's degree in technology, biological science, pharmacy, or other health-related discipline, or equivalent years of professional experience
Minimum 1 year of experience in a GMP (Good Manufacturing Practice) environment
Knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
Experience with quality management systems and processes in a clinical or pharmaceutical setting
Strong communication, organization, and problem-solving skills

Preferred Qualifications

Experience in clinical research, pharmaceutical industry, or Clinical Research Organization (CRO) environments
Familiarity with Logistics Quality Management (LQM) support functions
Experience with quality management systems and documentation
Background in depot, warehouse, or supply chain quality operations

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 hourly pay range for this role is $24hr to $33hr. The actual hourly salary pay 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

Refine Your Search

pharmacy site jobs in easton pa

Quality Specialist I Logistics

Hospice Medical Records

VP, QA Franchise (Med Device)

Mold Shop Machinist-Tool & Die Maker (2nd Shift)

Veterinary Technician

Field Reimbursement Manager

Regional Healthcare Sales Executive

Quality Manager, Logistics

Microbiologist I 1st Shift

Clinical Educator (PT) - Evergreen

Pharmacy Technician FrameworkLTC Data Entry & Billing Specialist

Pharmacy Technician II - Per Diem - Shift/Hours Varies - Atlantic Health Hackettstown Medical Center, NJ

Production Technician

Pharmacy Site Manager

General Manufacturing Associate: (1st shift)

Product Manager I, AIS

Medication Reconciliation Technician

Specialty Pharmacy Technician - Part Time

Pharmacy IV Room Coordinator

Medical Assistant Float, Maternal Fetal Medicine (Per Diem)

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