10 дней назад
QC Microbiology Associate II (Microbiology)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
QC Microbiology Associate II (Microbiology): Performing microbiological testing and laboratory support for pharmaceutical and medical products with an accent on cGMP compliance, data integrity, and accurate sample documentation. Focus on testing finished products and environmental samples, maintaining laboratory equipment, reviewing results, and supporting regulated quality systems.
Location: Onsite in Irvine, California, United States. Schedule: Sunday–Tuesday/Wednesday, 5:30 p.m.–5:30 a.m., working three 12-hour shifts.
Company
develops and manufactures medical products and services for healthcare, including infusion therapy, pain management, nutrition, pharmacy compounding, wound care, and dialysis.
What you will do
- Perform microbiological testing of finished products, stability samples, environmental monitoring samples, and other laboratory samples.
- Receive, prepare, process, and document samples in accordance with approved procedures and cGMP requirements.
- Record, review, and compile laboratory results and supporting documentation.
- Support equipment calibration, qualification, preventive maintenance, troubleshooting, and routine laboratory operations.
- Verify test results and assist with improvements to laboratory procedures, test methods, and documentation.
- Maintain laboratory cleanliness, organization, safety, and regulatory compliance.
Requirements
- High school diploma or GED.
- At least one year of laboratory, microbiology, quality control, or related scientific experience.
- Strong attention to detail and documentation skills.
- Ability to follow written procedures and work in a regulated laboratory environment.
- Proficiency in recording data, preparing reports, and reviewing laboratory documentation.
- Ability to work independently, collaborate with a team, and work non-standard hours.
Nice to have
- Bachelor’s degree in Microbiology, Biology, Chemistry, or a related scientific discipline.
- Experience in pharmaceutical, biotechnology, medical device, or FDA-regulated environments.
- Familiarity with cGMP regulations, laboratory quality systems, and microbiological testing methods.
- Experience with laboratory investigations, equipment qualification, or continuous improvement.
Culture & Benefits
- Healthcare benefits and a 401(k) plan.
- Tuition reimbursement.
- Work in a regulated laboratory and manufacturing-support environment with required PPE and safety procedures.
- Physical work includes standing, walking, bending, laboratory equipment use, and occasional lifting of up to 20 pounds.
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