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 microbiologist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship.
Qualifications
Bachelor’s degree required; concentration in a scientific or applied discipline strongly preferred, with 3-5 years of experience in pharmaceutical microbiology related position required; or a MS with 1-2 years of experience
Required Skills and Experience
Solid microbiology foundation with experience in performing product testing
Proven technical writing skills (SOPs, protocols)
Desired Skills and Experience
Experience in the pharmaceutical/biotechnology industries preferred
Experience with environmental monitoring and water testing preferred
Responsibilities
MICROBIOLOGICAL PRODUCT ANALYSIS
Analyze samples and compile meaningful data
Perform Investigations and prepare/respond to CAPA
Review, revise Test Procedures/Standard Operating Procedures
Ad Hoc work
Rotational on-call assignments
MICROBIOLOGICAL ACTIVITIES Include (but not limited to)
Receive, verify & Log in samples
MLT
Method Suitability testing
Endotoxin testing
Return templates and shipping paperwork when and where appropriate
Compile and trend data
Prepare and ship materials offsite for ID/testing (when applicable)
Environmental monitoring
Stock culture management and quality control of same
Biological indicator management
Bioburden testing
Water sampling
Microbiological media management and quality control of same
Sterilization activities
Research experiments as deemed appropriate by client management
Method Validation/Qualification
Other microbiological activities
Rotational on-call assignments for responding to alarms
CALIBRATIONS
Execute “Before-Use” calibrations prior to performing testing
Review calibration data within the ELN
Prepare and submit equipment for calibrations (offsite or onsite)
Complete calibration/PM paperwork
PROCAL Entries
GMP ACTIVITIES
Prepare GMP documentation as requested by management
Perform laboratory sanitizations and ensure cleanliness of laboratory workspace
Perform equipment sanitizations (incubators / hoods / refrigerators)
Purchase supplies (GMP)
Prepare and send documents to Records Center
INVESTIGATIONS
Initiate, facilitate, and perform Investigations and NOEs (Notice of Event-NOE) for Environmental samples [NOE for Microbiological Environment Event (MEN)]
Inform management of non-conforming events
AUDITS
Participate in audits (Regulatory, In-house, Corporate)
Participate in self-inspections and safety inspections
Retrieve data when requested by Microbiology management
TRAINING
Complete assigned training when required
Ensure training is complete prior to performing tasks
The role is intended to be a 40 hours per week position.
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.

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 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.
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