QC Microbiology Associate, Environmental Monitoring

BioPhase Solutions is seeking a QC Microbiology Associate for Environmental Monitoring in Los Angeles, CA. The role involves microbiological testing and environmental monitoring in sterile product manufacturing, along with laboratory maintenance and documentation support. Candidates should have a Bachelor's in Microbiology or a related field and at least 1 year of experience in a cGMP setting. The position requires strong organizational skills and effective communication.
BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QC Microbiology Associate, Environmental Monitoring to work for a leading Greater Los Angeles area biopharmaceutical company.
Pay Rate: $20-30/hour depending on experience.
Summary:The QCM Associate will perform various microbiological facility environmental and utility monitoring (EM) support of sterile product manufacturing, to include sampling and testing of the collected samples. The incumbent may also support other microbiological test methods, equipment and laboratory support and maintenance, and assist with the drafting of SOPs, protocols and reports to support cell therapy manufacturing operations. Organizes daily workload schedule and relevant resource requirements. Participates in authoring complex, explicit documentation for cell therapy manufacturing operations. The QC Microbiology Associate will also play a critical role in working collaboratively with cell culture manufacturing technicians and associates in support of EM. Important aspects of this role include excellent organization skills, flexibility, and the ability to thrive in an efficient, highly interactive, goal-oriented team environment, and other duties may be assigned. Essential duties are performed with regular oversight of QC Microbiology Supervisor/QC Manager.
Responsibilities:Performs Environmental and Utilities Monitoring and Microbiological testing in support of manufacturing cleanroom facility.Responsible for routine sample testing under GMP or non-GMP modes, laboratory maintenance, and assist in method qualification/validations.Responsible for laboratory maintenance to include cleaning and sanitization of laboratory equipment, laboratory restocking of supplies and inventory.Assist with the drafting of SOPs and work instructions, data entry and reportingQualifications:Bachelors in Microbiology or scientific related field1+ years of relevant experience within a cGMP Quality Control setting, preferably in the pharmaceutical or biotechnology industryExperience in cGMP aseptic processing facility is a plusGood understanding and demonstration of aseptic techniques.Communication skills: foster open communication, active listening and good communication skills; Good written and verbal communication skillsDemonstrates excellent attention to detail, can work quickly and accurately, organizing tasks and delivering quality with efficiency.Responsibilities outside of initial job descriptionPlease send resumes to tiffany@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities!!!