2 дня назад
Associate Scientist, Microbiology
60 200 - 100 400$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Associate Scientist, Microbiology (GMP/Environmental Monitoring): Performing microbiological testing and environmental monitoring to support the quality and development of biological therapeutics with an accent on GMP methods, aseptic technique, and data integrity. Focus on qualifying microbiological methods, analyzing bioburden and endotoxin results, and documenting testing for manufacturing and clinical supplies.
Location: Onsite in St. Louis, Chesterfield, Missouri, United States. Monday–Friday, first shift; occasional weekend or off-shift work may be required. Weekly manufacturing-area monitoring requires qualification in cleanroom gowning.
Annual base salary: $60,200–$100,400, plus eligibility for a 7.5% bonus target.
Company
develops medicines and vaccines through research, development, and manufacturing operations.
What you will do
- Apply GMP microbiological methods, including bioburden, endotoxin, PCR, and related testing, to assess product quality and detect impurities.
- Perform microbiology identification, testing, method qualification, validation, and characterization for biological therapeutics.
- Conduct and document environmental monitoring of manufacturing areas, water systems, and compressed gases.
- Analyze data independently, draw conclusions, present results, and propose solutions to technical problems.
- Review and contribute to validation protocols and reports, analytical procedures, investigations, trend reports, and change controls.
- Follow SOPs, GMP/GLP requirements, data-integrity standards, and applicable safety practices.
Requirements
- Bachelor’s degree in microbiology, biochemistry, biology, or a related field, plus 0–2 years of experience.
- Excellent documentation skills and strong attention to detail.
- Strong organizational, interpersonal, and written communication skills.
- Ability to work effectively in a team, follow established procedures, and operate with minimal supervision.
- Ability to perform repetitive laboratory work with micropipettes and periods of standing, sitting, or walking.
- Must have permanent authorization to work in the United States; visa sponsorship is not available now or in the future.
Nice to have
- Experience with quality systems in a GMP environment.
- Experience with LIMS, analytical instruments, or pharmaceutical laboratory work.
- Knowledge of biological drug development, regulatory requirements, and guidelines.
- Experience managing multiple tasks or projects and using generative AI tools responsibly to support problem solving.
Culture & Benefits
- Work in a research and development organization supporting biological therapeutics and clinical supplies.
- Benefits include a 401(k) plan with company contributions and retirement savings contributions.
- Paid vacation, holidays, personal days, caregiver and parental leave, and medical leave.
- Medical, prescription drug, dental, and vision coverage.
- Relocation assistance may be available based on business needs and eligibility.
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