5 дней назад
Quality Technician II, QC Aseptic (Biotechnology)
22 - 31$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Quality Technician II, QC Aseptic (Biotechnology): Performing environmental monitoring and microbial sampling in classified and non-classified areas to support sterile manufacturing operations with an accent on aseptic environments, cGMP documentation, and sample analysis. Focus on maintaining compliant laboratory activities, following SOPs, identifying deviations, and supporting technician training.
Location: West Chester, Ohio, USA; onsite
Salary: $21.50–$30.50 per hour
Company
is a technology-focused biomanufacturing company developing high-tech, end-to-end manufacturing solutions for pharmaceutical production.
What you will do
- Perform environmental monitoring, microbial sampling, visual inspections, and sample analysis in classified and non-classified areas, including Class 100/ISO 5 aseptic environments.
- Use environmental monitoring, sampling, and testing systems to collect samples, analyze results, and enter data.
- Document activities, results, sample receipts, laboratory records, and quality records in accordance with documentation practices.
- Follow SOPs, control documents, work instructions, cGMP requirements, and the quality management system.
- Maintain laboratory areas and equipment in a compliant state and report deviations or non-conformances.
- Audit SOPs and work instructions, recommend corrective activities, and support training for new technicians.
Requirements
- Ability to follow written procedures, SOPs, and work instructions with minimal supervision and escalate issues when needed.
- Strong attention to detail, accurate recordkeeping, and ability to perform mathematical calculations.
- Ability to read, write, speak, and follow instructions in English.
- High school, vocational school, or equivalent education.
- Ability to work a 12-hour 2/2/3 schedule from 6:00 a.m. to 6:30 p.m., with 24/7 on-call support as needed.
- Ability to perform non-sedentary physical work, use required PPE, and handle potential chemical exposure according to SOPs.
Nice to have
- At least one year of experience in pharmaceutical, biotechnology, or cGMP-regulated manufacturing.
- Working knowledge of Microsoft applications, MODA, LIMS, Novatek, or equivalent sampling and testing software.
- Experience in LEAN manufacturing.
- Knowledge of cGMPs and FDA policies and procedures.
Culture & Benefits
- Full-time employment with an annual cash bonus program.
- 401(k) plan with company match.
- Medical, dental, vision, life, and disability insurance.
- Paid vacation, holidays, and other leaves of absence.
- Tuition reimbursement and caregiving support.
- Work authorization and visa sponsorship are not available for this position.
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