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10 часов Π½Π°Π·Π°Π΄

Manufacturing Technician II - Sterile Filling

21 - 32$
Π€ΠΎΡ€ΠΌΠ°Ρ‚ Ρ€Π°Π±ΠΎΡ‚Ρ‹
onsite
Π’ΠΈΠΏ Ρ€Π°Π±ΠΎΡ‚Ρ‹
fulltime
Π“Ρ€Π΅ΠΉΠ΄
middle
Английский
b2
Π‘Ρ‚Ρ€Π°Π½Π°
US
Вакансия ΠΈΠ· списка Hirify.GlobalВакансия ΠΈΠ· Hirify Global, списка ΠΌΠ΅ΠΆΠ΄ΡƒΠ½Π°Ρ€ΠΎΠ΄Π½Ρ‹Ρ… tech-ΠΊΠΎΠΌΠΏΠ°Π½ΠΈΠΉ
Для мэтча ΠΈ ΠΎΡ‚ΠΊΠ»ΠΈΠΊΠ° Π½ΡƒΠΆΠ΅Π½ Plus

ΠœΡΡ‚Ρ‡ & Π‘ΠΎΠΏΡ€ΠΎΠ²ΠΎΠ΄

Для мэтча с этой вакансиСй Π½ΡƒΠΆΠ΅Π½ Plus

ОписаниС вакансии

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TL;DR
Manufacturing Technician II - Sterile Filling (Biomanufacturing): Operating and sanitizing sterile filling equipment, performing in-process checks, filter integrity testing, documentation, and batch record entries in a cGMP cleanroom environment with an accent on aseptic processing, equipment operation, and quality compliance. Focus on executing media fills, maintaining gowning qualifications, supporting validation and preventive maintenance, and improving production processes through lean activities.

Location: West Chester, Ohio, United States; onsite work in controlled and classified cleanroom production areas. Schedule: 12-hour 2/2/3 night shift.

Base pay: $21.50–$32.00 per hour, depending on location, experience, qualifications, skills, and knowledge.

Company

Technology-focused biomanufacturing company developing end-to-end manufacturing solutions for pharmaceutical production.

What you will do

  • Operate, assemble, disassemble, adjust, and sanitize sterile filling equipment.
  • Perform filter integrity testing, equipment start-up, material handling, printing, and in-process and finished-product inspections.
  • Complete SCADA and HMI data entries, batch records, GMP documentation, logs, calculations, and limited SAP inventory reconciliation.
  • Maintain cleanroom standards through cleaning, housekeeping, aseptic behaviors, gowning, media fills, and viable and non-viable monitoring.
  • Support preventive maintenance, validation and engineering protocols, cross-training, and daily tier meetings.
  • Participate in 5S, problem-solving, and process improvement while maintaining cGMP compliance.

Requirements

  • Previous experience in a regulated manufacturing environment; 1+ years in pharmaceutical, biotechnology, or cGMP manufacturing is preferred.
  • English proficiency sufficient to read, write, speak, and understand SOPs, batch records, and work instructions.
  • Accurate documentation and data-entry skills, including batch records and logbooks.
  • Basic mathematical and problem-solving skills, with the ability to follow procedures and escalate deviations.
  • Ability to work in a fast-paced production environment and complete required certifications, including aseptic gowning qualification.
  • Ability to perform physically demanding work, use PPE, pass an onboarding eye exam, and participate in occupational health requirements.

Nice to have

  • High school, vocational school, or equivalent education.
  • Knowledge of cGMP principles, lean manufacturing, Microsoft applications, SAP, or Veeva Vault.

Culture & Benefits

  • Annual cash bonus program and 401(k) plan with company match.
  • Medical, dental, vision, family-building, life, and disability benefits.
  • Paid vacation, holidays, and other leaves of absence.
  • Tuition reimbursement and caregiving support.
  • Work requires adherence to the Quality Management System, SOPs, cGMPs, safety procedures, and cleanroom requirements.

Π‘ΡƒΠ΄ΡŒΡ‚Π΅ остороТны: Ссли Ρ€Π°Π±ΠΎΡ‚ΠΎΠ΄Π°Ρ‚Π΅Π»ΡŒ просит Π²ΠΎΠΉΡ‚ΠΈ Π² ΠΈΡ… систСму, ΠΈΡΠΏΠΎΠ»ΡŒΠ·ΡƒΡ iCloud/Google, ΠΏΡ€ΠΈΡΠ»Π°Ρ‚ΡŒ ΠΊΠΎΠ΄/ΠΏΠ°Ρ€ΠΎΠ»ΡŒ, Π·Π°ΠΏΡƒΡΡ‚ΠΈΡ‚ΡŒ ΠΊΠΎΠ΄/ПО, Π½Π΅ Π΄Π΅Π»Π°ΠΉΡ‚Π΅ этого - это мошСнники. ΠžΠ±ΡΠ·Π°Ρ‚Π΅Π»ΡŒΠ½ΠΎ ΠΆΠΌΠΈΡ‚Π΅ "ΠŸΠΎΠΆΠ°Π»ΠΎΠ²Π°Ρ‚ΡŒΡΡ" ΠΈΠ»ΠΈ ΠΏΠΈΡˆΠΈΡ‚Π΅ Π² ΠΏΠΎΠ΄Π΄Π΅Ρ€ΠΆΠΊΡƒ. ΠŸΠΎΠ΄Ρ€ΠΎΠ±Π½Π΅Π΅ Π² Π³Π°ΠΉΠ΄Π΅ β†’