When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
We are looking to fill a Laboratory Associate position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in West Point, PA within their Regulated Bioanalytical Group. The laboratory associate will provide essential laboratory support for regulated bioanalytical studies conducted under Good Laboratory Practice (GLP). This role focuses on the preparation of solutions and reagents, handling and preparation of regulated biological samples, and execution of routine laboratory tasks in accordance with approved methods, SOPs, and regulatory requirements. The lab associate works under close supervision and contributes to the timely and compliant generation of high-quality bioanalytical data. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship.
Responsibilities
Laboratory Operations and Sample Handling
• Prepare buffers, solutions, standards, controls, and reagents per approved procedures.
• Receive, log, aliquot, label, store, and track biological samples in compliance with GLP requirements.
• Support sample preparation and basic assay execution under supervision.
Compliance and Documentation
• Perform all work in accordance with GLP, SOPs, and safety procedures.
• Accurately complete laboratory notebooks, worksheets, logbooks, and electronic records.
• Maintain data integrity following established documentation practices.
Equipment and Laboratory Support
• Assist with routine laboratory maintenance, cleaning, and inventory monitoring.
• Operate basic laboratory equipment after training and qualification.
• Report equipment issues, deviations, or unexpected observations to senior staff.
Team and Development
• Work effectively within a team-based regulated laboratory environment.
• Demonstrate a learning mindset and actively build technical and regulatory knowledge.
Qualifications -
A.S. in Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, or related scientific discipline (or equivalent laboratory experience)
Required Skills and Experience
Basic understanding of laboratory techniques and scientific principles.
Strong attention to detail and ability to follow written procedures precisely.
Willingness to work in a regulated environment and adhere to strict compliance standards.
Desired Skills and Experience
Prior experience in a regulated laboratory environment (GLP, GMP, or GxP).
Hands-on experience with solution or reagent preparation and biological sample handling.
Familiarity with basic laboratory documentation practices.
About Parexel
Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies.
For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement.
Come join us!
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EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
