23 часа назад
Manufacturing Process Technician (Biotech Manufacturing)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Manufacturing Process Technician (Biotech Manufacturing): Performing bulk manufacturing processes in aseptic and non-aseptic environments with an accent on equipment operation, material handling, cleaning, sampling, and GMP documentation. Focus on monitoring clean systems and autoclaves, preparing and transferring solutions, completing electronic batch records, and maintaining accuracy during rotating 12-hour shifts.
Location: West Greenwich, Rhode Island, United States; onsite manufacturing role with rotating 12-hour shifts from 7am to 7pm, covering 7 days per week on a two-week rotation.
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, and set up and break down single-use materials.
- Weigh and dispense raw materials, prepare and transfer solutions, and handle manufacturing materials.
- Operate and monitor clean systems, autoclaves, and processing equipment, including power industrial vehicles.
- Collect, process, store, and deliver samples, and reconcile products and components.
- Complete process documentation accurately, perform calculations, and follow current Good Manufacturing Practices.
Requirements
- High school diploma/GED plus 1 year of manufacturing, operations, or military experience, or an associate degree.
- Ability to assemble, disassemble, operate, and understand simple to moderately complex equipment according to procedures.
- Basic understanding of measurements, calculations, and the metric system.
- Ability to stand or sit for extended periods, maintain focus during repetitive tasks, and perform work with close attention to detail.
- Ability to follow written procedures, recognize and report malfunctions, complete electronic batch records, and communicate effectively.
- Ability to work a rotating 12-hour shift schedule from 7am to 7pm.
Nice to have
- Experience in a GMP or other regulated environment.
- Knowledge of GMP principles and drug substance manufacturing experience.
- Ability to receive coaching and demonstrate measurable improvement.
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, work-life balance support, and career development opportunities.
- Inclusive, collaborative, science-based work environment focused on serving patients.
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