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14 часов Π½Π°Π·Π°Π΄

Manufacturing Associate I and II (Biopharma)

79Β 000 - 102Β 500$
Π€ΠΎΡ€ΠΌΠ°Ρ‚ Ρ€Π°Π±ΠΎΡ‚Ρ‹
onsite
Π’ΠΈΠΏ Ρ€Π°Π±ΠΎΡ‚Ρ‹
fulltime
Π“Ρ€Π΅ΠΉΠ΄
junior/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

ВСкст:
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TL;DR
Manufacturing Associate I and II (Biopharma): Executing cGMP manufacturing operations for oncolytic immunotherapy products with an accent on aseptic processing, single-use technologies, and production documentation. Focus on preparing buffers, operating filtration and filling equipment, supporting viral production, and maintaining manufacturing readiness in a cleanroom environment.

Location: Framingham, Massachusetts, United States; on-site

Salary: $79,000–$102,500 annual base pay, plus performance incentive bonus and equity eligibility.

Company

hirify.global develops oncolytic immunotherapies designed to activate durable systemic anti-tumor responses and transform cancer treatment.

What you will do

  • Execute cGMP manufacturing operations supporting production at the Framingham facility.
  • Author and revise SOPs, batch records, deviations, and other manufacturing documentation.
  • Perform aseptic operations in biosafety cabinets and cleanroom environments, including gowning and sterile gowning.
  • Assemble, clean, and autoclave process components and equipment; prepare buffers and solutions.
  • Set up and operate single-use equipment for viral production, tangential flow filtration, chromatography, filtration, and aseptic filling.
  • Support equipment validation and commissioning, routine maintenance, visual inspection, inventory, and manufacturing suite cleaning.

Requirements

  • Bachelor’s degree with 1–3 years of related cGMP biopharma manufacturing experience, or an associate’s degree/high school diploma with 3–6 years of related experience.
  • At least 1 year of manufacturing experience in a cGMP environment.
  • Experience in cell culture, drug substance purification, or aseptic filling.
  • Experience with single-use manufacturing technologies and Microsoft Word and Excel.
  • Strong organizational, communication, attention-to-detail, and teamwork skills.
  • Availability for occasional weekend or holiday work based on production needs.

Culture & Benefits

  • Collaborative, bold, dedicated, and candid working environment focused on patient impact.
  • Medical, dental, and vision insurance.
  • 401(k) match, flexible time off, and paid holidays including a year-end shutdown.
  • Annual performance incentive bonus, new-hire equity, and ongoing performance-based equity.

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†’