3 дня назад
QC Microbiology Associate I (Pharmaceutical Manufacturing)
23 - 28$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
QC Microbiology Associate I (Pharmaceutical Manufacturing): Performing routine microbiological testing and laboratory support for pharmaceutical products and manufacturing processes with an accent on environmental monitoring, microbial testing, cGMP compliance, and accurate documentation. Focus on investigating OOS/OOT results and laboratory deviations, maintaining qualified equipment, and improving microbiology test methods and SOPs.
Location: Onsite in Irvine, California, United States. Schedule: Sunday–Tuesday or Wednesday, 5:30 p.m.–5:30 a.m., working 3 or 4 12-hour shifts.
Salary: $23.68–$28.37 per hour.
Company
develops and manufactures healthcare products and services focused on infusion therapy, pain management, nutrition, pharmacy compounding, wound care, ostomy care, and dialysis.
What you will do
- Perform microbiological testing for finished products, stability studies, utilities, raw materials, and environmental monitoring samples.
- Receive, prepare, incubate, enumerate, identify, and document microbiological samples and test results.
- Record, review, and maintain laboratory data in accordance with cGMP, laboratory procedures, and data integrity standards.
- Maintain laboratory equipment, media, reagents, and supplies to support uninterrupted testing.
- Assist with equipment qualification, calibration, preventive maintenance, troubleshooting, and performance monitoring.
- Support OOS, OOT, and laboratory deviation investigations, as well as improvements to test methods and SOPs.
Requirements
- High school diploma or GED required; an associate degree in microbiology, biology, biotechnology, or a related discipline is preferred.
- 0–2 years of experience in microbiology, laboratory, pharmaceutical, medical device, biotechnology, or another regulated environment.
- Basic knowledge of microbiological techniques, aseptic practices, and laboratory safety procedures.
- Ability to follow written procedures and accurately document laboratory activities.
- Strong attention to detail, organization, teamwork, and ability to manage multiple priorities.
- Basic computer proficiency, including Microsoft Office applications.
Nice to have
- Experience in a cGMP-regulated pharmaceutical, medical device, or biotechnology environment.
- Hands-on experience with environmental monitoring, bioburden testing, microbial identification, or sterility testing.
- Familiarity with laboratory systems, data management software, electronic documentation, USP microbiological testing, and contamination control.
Culture & Benefits
- Collaboration with Quality, Manufacturing, Technical Services, supervisors, and laboratory peers.
- Work within a team-oriented environment focused on product quality, patient safety, and regulatory compliance.
- Healthcare benefits and a 401(k) plan.
- Tuition reimbursement.
- Continuous improvement supported through ’s Sharing Expertise initiative.
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