6 часов назад
RMF Senior Production Technician (Biopharmaceutical Manufacturing)
24 - 34$
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
RMF Senior Production Technician (Biopharmaceutical Manufacturing): Supporting the startup, qualification, validation, and commercial operation of a cGMP manufacturing facility for Flublok/Panblok drug substance with an accent on equipment setup, electronic manufacturing systems, production documentation, and cross-functional execution. Focus on commissioning manufacturing equipment, executing qualification and production runs, maintaining inspection readiness, and troubleshooting production processes.
Location: Swiftwater, Pennsylvania, United States; onsite, third shift. The role may require work across multiple buildings, modified shifts, weekends, holidays, and overtime.
Salary: $24.34–$32.45 per hour
Company
is an R&D-driven biopharmaceutical company developing medicines and vaccines, including products that address infectious diseases.
What you will do
- Support commissioning, setup, testing, qualification, and validation of manufacturing equipment for the B55 Recombinant Manufacturing Facility.
- Prepare manufacturing spaces and equipment for engineering runs, process qualification runs, and cGMP commercial production of Flublok/Panblok drug substance.
- Operate and document cGMP manufacturing activities, including equipment setup, cleaning, sterilization, upstream and downstream processing, and material preparation.
- Support MES, eLogbooks, eBRs, SAP, LIMS, Labwatch, Documentum, Metasys, and DeltaV activities.
- Collaborate with engineering, validation, quality assurance, quality control, manufacturing technology, and external stakeholders.
- Train and guide operations personnel, support investigations, CAPAs, change controls, process improvements, and production issue resolution.
Requirements
- High school diploma or GED with at least 2 years of cGMP or pharmaceutical experience; or an associate degree with at least 1 year of experience; or a bachelor’s degree with no experience required.
- Experience or knowledge in cGMP, pharmaceutical or industrial quality operations.
- Mechanical aptitude, computer skills, troubleshooting ability, strong comprehension and retention, attention to detail, and manual dexterity.
- Ability to lift up to 50 pounds, stand for approximately 8 hours per shift, gown, and enter manufacturing areas.
- Ability to work flexible and off-shift schedules and potentially support aseptic processing areas and N95 fit testing.
- Applicants are limited to US and Puerto Rico residents.
Nice to have
- Experience with batch record review, environmental monitoring, logbook review, technical writing, SAP, or PI Historian.
- Familiarity with media or buffer preparation, cell and virus stock production, bioreactors, centrifugation, chromatography, or filtration.
Culture & Benefits
- Work alongside cross-functional manufacturing and supply teams supporting vaccine production.
- Career development opportunities through promotion, lateral moves, and international opportunities.
- Employee rewards and benefits programs.
- Healthcare, prevention, and wellness benefits.
- At least 14 weeks of gender-neutral parental leave.
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