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Philadelphia, PA, United StatesPosted 109 months ago
Full-timehybridMid-Senior Level

Job Description

Following is the position details:

Title: Microbiologist - Permanent Position

Location: West Chester, PA.

Job Description:

We are seeking a highly motivated QC Microbiologist who is interested in joining our fast-paced, dynamic QC environment to perform microbiological sampling in support of Facility Utilities Monitoring and Environmental Monitoring Program in support of the GMP manufacturing facility of a cell therapy product including sampling of raw material and release testing.

Duties & Responsibilities

· Sampling Lead – Utililities, gases, EM and Raw Materials

· Submit micro identifications to CRO

· Responsible for daily scheduling of junior analyst sampling schedule

· Manage variable sample influx by potentially adjusting daily schedule

· Communicate expected sample test times and results with QC Lab Assistants

· Participate in aseptic processing in a clean room environment

· Performs environmental monitoring sampling of plant utilities and production clean zones using particle counters, contact plates and microbial air samplers

· Perform protocol driven studies for bioburden, endotoxin, , EM, Raw Materials -ID, etc

· Report testing results via Laboratory Inventory Management System (LIMS)

· Generating data to support site manufacturing and/or complaint investigations and resolving project-related questions

· Performs routine and non-routine microbiological testing such as water bioburden and media growth promotion; Gram staining and microbial identifications

· Performs enumeration and characterization of microorganisms recovered from samples

· Perform growth promotion

· Identifies bacteria and susceptibilities, molds, yeast, parasites, and other related organisms

· Perform Microbiological test methods for cell therapy product, raw material and release testing

Minimum Requirements

· B.S. in Biology/Microbiology, or related sciences with 3-5 years of related experience.

· Previous working experience in a QC laboratory GMP manufacturing facility highly desirable

· Strong time management and organization skills are required

· Knowledge of regulatory requirements and standards (FDA, EU, ICH, ISO, USP) a plus

· Aseptic technique or cleanroom experience desired

· The ability to work off-shift hours, based on business needs, is required

· Able to work independently with minimum supervision

· Good accurate and clear documentation skills is required

BS/MS in biology or microbiology

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus


Thank you for your time and consideration. I look forward to hearing from you!

Regards,

Neha Thakur

Life Sciences Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

(Direct) 732-844-8735

www.irionline.com

Gold Seal JCAHO Certified ™ for Health Care Staffing

“INC 5000’s FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)


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Microbiologist at Integrated Resources INC | Renata