6 дней назад
Manufacturing Process Technician - Nights (Biotech Manufacturing)
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Manufacturing Process Technician - Nights (Biotech Manufacturing): Performing bulk drug-substance manufacturing processes in aseptic and non-aseptic environments with an accent on GMP compliance, equipment operation, materials handling, and electronic batch-record documentation. Focus on operating clean systems and autoclaves, managing cryogenic systems, completing process calculations, and maintaining accurate manufacturing records during the night shift.
Location: West Greenwich, Rhode Island, United States; onsite night-shift role
Company
is a biotechnology company researching, manufacturing, and delivering medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.
What you will do
- Perform simple to moderately complex bulk-manufacturing processes according to standard operating procedures and batch records.
- Clean equipment and parts using manual and automated methods in aseptic and non-aseptic environments.
- Set up and break down single-use materials, weigh and dispense raw materials, and handle manufacturing materials.
- Operate and monitor clean systems, autoclaves, processing equipment, cryogenic systems, and power industrial vehicles.
- Collect, process, store, and deliver samples; reconcile products and components.
- Complete process documentation, calculations, CIP and SIP operations, and other assigned manufacturing tasks in accordance with current GMP requirements.
Requirements
- High school diploma or GED plus at least one year of manufacturing or operations experience, or military experience; alternatively, an associate's degree.
- Ability to follow written procedures, recognize and report malfunctions, and accurately complete electronic batch records.
- Ability to operate, assemble, and disassemble simple to moderately complex equipment.
- Basic understanding of measurements, calculations, and the metric system.
- Ability to stand or sit for extended periods, maintain focus during repetitive tasks, and work with strong attention to detail.
- Ability to work independently and in a team, communicate effectively, and respond constructively to coaching.
Nice to have
- At least one year of experience in a GMP or other regulated environment.
- Knowledge of GMP principles and drug-substance manufacturing experience.
Culture & Benefits
- Health, dental, and vision coverage, life and disability insurance, and flexible spending accounts.
- Retirement and savings plan with company contributions.
- Discretionary annual bonus program and stock-based long-term incentives.
- Paid time-off plans and career development opportunities.
- Collaborative, innovative, science-based work environment focused on serving patients.
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