4 дня назад
QC Microbiology Assoc II (Sun-Tues/Wed 5:30pm-5:30am)
26 - 31$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
QC Microbiology Associate II (Microbiology/Quality Control): Performing microbiological testing and laboratory support for finished products, stability samples, environmental monitoring, and other samples with an accent on cGMP compliance, data integrity, and accurate documentation. Focus on verifying laboratory results, maintaining and qualifying equipment, supporting investigations and continuous improvement, and operating safely in a regulated pharmaceutical manufacturing environment.
Location: Onsite in Irvine, California, United States. Schedule: Sunday–Tuesday/Wednesday, 5:30 p.m.–5:30 a.m.; 3/4 × 12-hour shifts. Relocation is not available.
Salary: $26.00–$31.00 per hour.
Company
develops, manufactures, and markets medical products and services for infusion therapy, pain management, nutrition, pharmacy admixture, wound care, dialysis, and related healthcare applications.
What you will do
- Perform microbiological testing of finished products, stability samples, environmental monitoring samples, and other laboratory samples.
- Receive, prepare, process, document, review, and compile samples, results, reports, and supporting records.
- Maintain data integrity and ensure testing complies with cGMP requirements, approved methods, specifications, and quality standards.
- Support equipment calibration, qualification, preventive maintenance, troubleshooting, and routine laboratory operations.
- Assist with laboratory investigations, procedure and test-method revisions, and continuous improvement initiatives.
- Maintain laboratory cleanliness, organization, safety, and regulatory compliance while working with laboratory equipment and biological materials.
Requirements
- High school diploma or GED.
- At least one year of laboratory, microbiology, quality control, or related scientific experience.
- Strong attention to detail and accurate documentation and recordkeeping skills.
- Ability to follow written procedures and work independently and collaboratively in a regulated environment.
- Proficiency in data recording, report preparation, and laboratory documentation review.
- Ability to work onsite in Irvine and cover the specified overnight Sunday–Wednesday schedule.
Nice to have
- Bachelor’s degree in microbiology, biology, chemistry, or a related scientific discipline.
- Experience in pharmaceutical, biotechnology, medical device, or other 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
- Work in a laboratory and pharmaceutical manufacturing support environment with required PPE and safety procedures.
- Healthcare benefits and a 401(k) plan.
- Tuition reimbursement.
- Continuous improvement is supported through the Sharing Expertise initiative.
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