8 дней назад
Quality Control Lab Technician
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Quality Control Lab Technician (Analytical Chemistry): Conducting routine and non-routine testing of raw materials, in-process materials, and finished goods with an accent on chromatographic analysis, laboratory instrumentation, and GMP-compliant quality control. Focus on troubleshooting and maintaining instruments, investigating deviations and OOS results, supporting CAPA, and executing method validation and transfer activities.
Location: On-site in Pensacola, Florida, United States
Company
Cytiva is a operating company providing life-science, diagnostics, and biotechnology solutions that support biological research, vaccines, medicines, and cell and gene therapies.
What you will do
- Perform routine and non-routine testing of raw materials, in-process materials, and finished goods using Karl Fischer titration, Buchi IPA extraction, GC, HPLC, IC, FTIR, wet chemistry, sample preparation, and data analysis.
- Analyze and trend laboratory data in Microsoft Excel and prepare clear technical documentation and reports.
- Operate, calibrate, troubleshoot, and maintain laboratory instruments while documenting and reviewing data under GMP, GLP, GDP, ISO, and applicable regulatory requirements.
- Investigate laboratory deviations and out-of-specification results, support CAPA activities, and contribute to continuous improvement.
- Support method validation, verification, and transfer through protocol execution, data collection, statistical analysis, and technical reporting.
Requirements
- Bachelor’s degree in Chemistry, Biology, or a related scientific discipline.
- 3+ years of laboratory experience, preferably in a regulated pharmaceutical, medical-device, manufacturing, food, environmental, or quality-testing environment.
- Hands-on experience with analytical instrumentation, wet chemistry, laboratory testing, and instrument troubleshooting.
- Strong analytical, organizational, problem-solving, communication, and independent-working skills with close attention to detail.
- Proficiency in Microsoft Excel and Word.
- Ability to travel up to 10%, stand for extended periods, and lift, move, or carry equipment weighing up to 50 lbs.
Nice to have
- Working knowledge of cGMP, GLP, GDP, ISO 17025, ISO 9001, ISO 13485, or similar quality management systems.
- Experience writing, revising, or auditing Quality Management System documentation.
- Lean, Six Sigma, or other continuous improvement training or certification.
Culture & Benefits
- Culture focused on belonging, learning, innovation, and continuous improvement.
- Paid time off and medical, dental, and vision insurance for eligible employees.
- 401(k) benefits for eligible employees.
- Eligibility for bonus or incentive pay.
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