6 дней назад
Quality Associate I, Microbiology
68 000 - 93 500$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Quality Associate I, Microbiology (Microbiology/Pharmaceutical Quality): Supporting microbiological testing of pharmaceutical products, raw materials, environmental samples, and critical facility systems with an accent on aseptic techniques, sterility and endotoxin testing, and cGMP compliance. Focus on environmental monitoring, laboratory investigations, data integrity, and improving laboratory efficiency through LEAN practices.
Location: Round Lake, Illinois, United States. Onsite at the Round Lake manufacturing facility; first shift, Tuesday–Saturday, with occasional off-shift and holiday work.
Salary: $68,000–$93,500 annually, with potential eligibility for discretionary bonuses.
Company
develops and manufactures healthcare and pharmaceutical products focused on saving and sustaining lives.
What you will do
- Conduct biological testing of raw materials, in-process samples, finished products, and environmental monitoring samples.
- Perform sterility, endotoxin, facility environmental, and critical systems monitoring for water, clean steam, compressed air, and nitrogen.
- Prepare laboratory media and reagents and operate instruments such as particle counters, pH meters, SAS units, and autoclaves.
- Record and analyze data in LIMS, prepare quality-system trend reports, and maintain data integrity.
- Author and revise laboratory procedures and investigations, support audits, and update plant SOPs.
- Support LEAN improvement projects, inventory management, preventative maintenance, housekeeping, and laboratory operations across Drug Delivery and Penicillin facilities.
Requirements
- Bachelor’s degree in microbiology or an equivalent degree with biology or microbiology laboratory coursework, plus 0–2 years of laboratory experience.
- Proficiency with LIMS and knowledge of basic biology, microbiology, and aseptic technique.
- Must not be allergic to penicillin, cephalosporin, or related products and minerals.
- Ability to work independently and collaboratively, manage multiple tasks, communicate issues, and maintain attention to detail.
- Ability to lift up to 50 pounds when required and comply with company SOPs, safety requirements, FDA, QSR, and cGMP regulations.
- Applicants must already be authorized to work for any employer in the United States; visa sponsorship is not available.
Nice to have
- Knowledge of GLP and pharmaceutical aseptic-processing cGMP requirements.
Culture & Benefits
- Collaborative quality organization with opportunities to work independently and contribute to manufacturing improvements.
- Medical and dental coverage beginning on day one, plus life, disability, and travel accident insurance.
- 401(k) retirement plan with company matching, employee stock purchase plan, flexible spending accounts, and educational assistance.
- Paid holidays, paid time off, family and medical leave, paid parental leave, childcare benefits, and employee assistance resources.
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